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Genentech's Medicine Avastin Plus Chemotherapy Improved Survival in Women with Advanced Cervical Cancer, Compared to Chemotherapy Alone
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Genentech Announces Final Phase III Study Results of Avastin Plus Radiotherapy and Chemotherapy in People with an Aggressive Form of Brain Cancer
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Genentech's Obinutuzumab (GA101) Significantly Reduced the Risk of Disease Progression or Death in People with One of the Most Common Forms of Blood Cancer
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Genentech to Present Important New Data Reflecting Broad Cancer Pipeline at ASCO
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FDA Approves Tarceva (Erlotinib) Tablets and Cobas EGFR Mutation Test for Specific Type of Lung Cancer
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FDA Approves ACTEMRA® for Children Living with a Rare Form of Arthritis
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Phase III Results Showed omalizumab Significantly Reduced Disease Severity in Patients with a Chronic form of Hives who Failed Standard Therapy
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FDA Approves Genentech's Kadcyla (Ado-Trastuzumab Emtansine), the First Antibody-Drug Conjugate for Treating Her2-Positive Metastatic Breast Cancer
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Obinutuzumab (GA101) Significantly Improved Progression-Free Survival in People With Chronic Lymphocytic Leukemia (CLL)
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FDA Approves New Use of Avastin Plus Chemotherapy for People with Metastatic Colorectal Cancer
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Genentech Announces FDA Approval of Tamiflu for the Treatment of Influenza in Infants
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Genentech's Perjeta Significantly Extends Survival in People With HER2-Positive Metastatic Breast Cancer
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Genentech Study Showed That Avastin Helped People with Newly Diagnosed Glioblastoma Live Longer without Their Disease Worsening When Added to Radiation and Chemotherapy
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ADACTA Study Showed ACTEMRA Improved Signs and Symptoms of Rheumatoid Arthritis Significantly More Than Adalimumab as a Single-Agent Therapy
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FDA Grants Genentech's Trastuzumab Emtansine (T-DM1) Priority Review for HER2-Positive Metastatic Breast Cancer
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FDA Approves Expanded Indication for ACTEMRA® in Rheumatoid Arthritis
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Genentech's Trastuzumab Emtansine (T-DM1) Significantly Extended Survival in People With Aggressive Form of Breast Cancer
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New Data from Phase III EMILIA Study Showed Genentech's Trastuzumab Emtansine (T-DM1) Significantly Improved Survival of People With HER2-Positive Metastatic Breast Cancer
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FDA Approves Lucentis® (Ranibizumab Injection) for Treatment of Diabetic Macular Edema (DME)
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Genentech Study Showed That Adding Avastin to Radiation and Chemotherapy Significantly Extended the Time People with an Aggressive Form of Brain Cancer Lived without Their Disease Worsening
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Genentech Reports Second Positive Study of ACTEMRA® Given by Subcutaneous Injection to Patients with Rheumatoid Arthritis
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FDA Advisory Committee Unanimously Recommends Approval of Lucentis for Treatment of Diabetic Macular Edema (DME)
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New Data From Phase III Study Showed That People With HER2-Positive Metastatic Breast Cancer Lived Longer With Genentech's Perjeta
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FDA Approves Perjeta (Pertuzumab) for People With HER2-Positive Metastatic Breast Cancer
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Genentech's ACTEMRA® Improved Rheumatoid Arthritis Signs and Symptoms Significantly More Than Adalimumab as Single-Agent Therapy
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Genentech Data Showed That People With Metastatic Colorectal Cancer Lived Longer When They Continued on Avastin Plus Chemotherapy
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Genentech's Targeted Investigational Breast Cancer Medicine, Trastuzumab Emtansine (T-DM1), Reduced the Risk of Cancer Worsening or Death by 35 Percent in Pivotal Phase III Trial
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Genentech Study Showed That Adding Avastin to Chemotherapy Cut the Risk of the Disease Getting Worse in Difficult-to-Treat Recurrent Ovarian Cancer by Half
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Genentech Will Report New Data on Important Progress for People with Advanced Cancers at ASCO 2012
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Genentech Reports Positive Study of ACTEMRA Given by Subcutaneous Injection
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Genentech's Trastuzumab Emtansine (T-DM1) Showed Positive Phase III Results In HER2-Positive Metastatic Breast Cancer
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Genentech's ACTEMRA® Monotherapy Showed Superior Improvement in Rheumatoid Arthritis Signs and Symptoms Versus Adalimumab Monotherapy
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FDA Grants Genentech's Pertuzumab Priority Review for Previously Untreated HER2-Positive Metastatic Breast Cancer
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FDA Approves Erivedge (Vismodegib) Capsule, the First Medicine for Adults with Advanced Basal Cell Carcinoma
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Genentech Announces First Milestone Payment to Device-Maker ForSight VISION4, Inc. in Development of Sustained Delivery Lucentis
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Genentech Announces Positive Results of Pivotal Phase III Study with Pertuzumab in HER2-Positive Metastatic Breast Cancer
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Genentech to Present Important New Data for HER2-Positive Breast Cancer at 2011 San Antonio Breast Cancer Symposium
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FDA Commissioner Announces Final Decision on Avastin for Metastatic Breast Cancer
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FDA Accepts Genentech's New Drug Application For Vismodegib in Advanced Form of Skin Cancer
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Data Showed ACTEMRA Monotherapy Significantly Improved Signs and Symptoms of Rheumatoid Arthritis
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Phase II Study Showed Ocrelizumab Maintained Significant Reduction in Disease Activity for Multiple Sclerosis Patients for Almost Two Years
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Genentech's Investigational Medicine T-DM1 Showed Improvement in Progression-Free Survival Compared to Standard of Care in HER2-Positive Metastatic Breast Cancer
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Genentech Submits New Drug Application to FDA for Vismodegib for Rare Form of Advanced Skin Cancer
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FDA Approves Zelboraf (Vemurafenib) and Companion Diagnostic for BRAF Mutation-Positive Metastatic Melanoma, a Deadly Form of Skin Cancer
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Pertuzumab Combined with Herceptin and Chemotherapy Significantly Extended the Time People with
HER2-Positive Metastatic Breast Cancer Lived without Their Disease Getting Worse
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Genentech Provides Update from FDA Hearing on Avastin for Metastatic Breast Cancer
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Two Pivotal Phase III Lucentis Studies Showed Patients With Diabetic Macular Edema Experienced Significant Improvements in Vision and Fewer Developed More Advanced Retinopathy
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Pivotal Study Showed Vismodegib Helped Shrink Tumors or Heal Lesions in People with Rare Form of Advanced Skin Cancer
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Genentech Announces Data to Show Avastin-Based Regimen Halved the Risk of Disease Getting Worse in Women with Recurrent Ovarian Cancer
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Genentech Announces Vemurafenib Improved Survival in People With Metastatic Melanoma Who Have BRAF V600 Mutations
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Tarceva Nearly Doubled the Time People with a Genetically Distinct Type of Lung Cancer Lived without Their Disease Getting Worse
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MetMAb in Combination with Tarceva Doubled the Time People with Lung Cancer Lived without Their Disease Getting Worse
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Genentech to Present Significant Progress in Advanced Skin, Lung and Ovarian Cancers at ASCO
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New Drug Applications Submitted in the United States and Europe for Vemurafenib in Advanced Skin Cancer
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FDA Approves Rituxan Plus a Steroid for Use in Severe Forms of Vasculitis
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FDA Approves ACTEMRA® (tocilizumab) for the Treatment of Systemic Juvenile Idiopathic Arthritis (SJIA)
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Second Lucentis Phase III Study Meets Primary Endpoint for Improved Vision in Patients with Diabetic Macular Edema (DME)
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Genentech Announces Positive Pivotal Phase II Results for Hedgehog Pathway Inhibitor in Advanced Basal Cell Carcinoma
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Phase III Study of Lucentis Showed Rapid Vision Improvements Sustained for Two Years in Patients with Diabetic Macular Edema
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FDA Grants Genentech a Hearing on Avastin's Use for Metastatic Breast Cancer in the United States
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Lucentis Phase III Study Meets Primary Endpoint For Improving Vision In Patients With Diabetic Macular Edema (DME)
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Third Phase III Study of Avastin-Based Regimen Met Primary Endpoint in Ovarian Cancer
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Early Successful Readout of Tarceva Study in a Distinct Form of Lung Cancer
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Genentech Personalized Investigational Medicine Shows Survival Benefit in Advanced Skin Cancer
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Genentech Informs Customers of Important Information About Triad Group's Alcohol Prep Pads
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FDA Grants Supplemental Approval for ACTEMRA® (tocilizumab)
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Genentech Provides Update on Avastin for Metastatic Breast Cancer Following Reviews in Europe and the United States
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Phase II Study with First-in-Class Investigational Drug Demonstrates Improvement in Negative Symptoms in Patients with Schizophrenia
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Pertuzumab and Herceptin Plus Chemotherapy Significantly Improved the Rate of Complete Tumor Disappearance in Study of Women with Newly Diagnosed, Early-Stage HER2-Positive Breast Cancer
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Phase III Study Showed Rituxan® for Initial Use Followed by Continued Use Delayed the Need for Additional Therapy in People with Asymptomatic Follicular Lymphoma, a Common Type of Blood Cancer
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FDA Approves Rituxan for First-Line Maintenance Use in Follicular Lymphoma
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ACTEMRA Data Presented at ACR Annual Meeting on Rapid Response and Long-Term Efficacy in People with Rheumatoid Arthritis
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Genentech Reports Promising Phase II Results With New Targeted Approach in Advanced Melanoma
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FDA Approves Herceptin For HER2-Positive Metastatic Stomach Cancer
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Phase II Study with Ocrelizumab Shows Significant Reduction in Disease Activity for Multiple Sclerosis Patients
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Genentech Provides Update on Avastin for Advanced Breast Cancer
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Genentech Provides Update on FDA Application for T-DM1
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FDA Approves Longer Use of Valcyte for Adult Kidney Transplant Patients at High Risk of Developing Cytomegalovirus (CMV) Disease
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Genentech Provides Update From Avastin FDA Advisory Committee Meeting
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Genentech Submits Application to FDA for Trastuzumab-DM1 in Previously Treated Advanced HER2-Positive Breast Cancer
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Second Phase III Study Showed Avastin-Containing Regimen Helped Women with Ovarian Cancer Live Longer Without their Disease Getting Worse
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FDA Approves Lucentis® (Ranibizumab Injection) for the Treatment of Macular Edema Following Retinal Vein Occlusion
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Phase III Study Showed Avastin-Based Regimen Helped Women with Advanced Ovarian Cancer Live Longer Without Their Disease Worsening
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Genentech's Scheller Wins Kavli Prize in Neuroscience
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Phase III Study Showed First-Line Maintenance Use of Rituxan® Improved the Likelihood of People with Follicular Lymphoma Living without Their Disease Worsening
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Roche and Genentech to Present New Data on Different Approaches to Treating Cancer at ASCO
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Genentech Submits Supplemental Application to FDA for Herceptin in Advanced HER2-Positive Stomach Cancer
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FDA Approves Tarceva as a Maintenance Therapy for Advanced Non-Small Cell Lung Cancer
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Genentech Submits Supplemental Biologics License Application for ACTEMRA (tocilizumab) for Prevention of Structural Joint Damage and Improvement of Physical Function in Rheumatoid Arthritis
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Genentech Provides Update on Phase III Study of Avastin in Men With Late Stage Prostate Cancer
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Genentech Announces Positive Results of Avastin Phase III Study in Women with Advanced Ovarian Cancer
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Phase III Study of Avastin Plus Chemotherapy in Advanced Stomach Cancer Did Not Meet Primary Endpoint
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FDA Approves Rituxan Plus Chemotherapy for the Most Common Type of Adult Leukemia
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FDA Extends Review Period for Tarceva Application for First-line Maintenance Use in Advanced Non-small Cell Lung Cancer
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FDA Approves ACTEMRA® (tocilizumab) for the Treatment of Moderately to Severely Active Rheumatoid Arthritis
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FDA Advisory Committee Recommends Against Approving Tarceva for First-Line Maintenance Use in Advanced Non-Small Cell Lung Cancer
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New Phase II Study Showed Trastuzumab-DM1 Shrank Tumors in Women With Highly Advanced HER2-positive Breast Cancer
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Avastin Plus Commonly Used Chemotherapies Improved Progression-Free Survival in Women Previously Treated with Chemotherapy for Advanced Breast Cancer
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Genentech and Biogen Idec Announce Positive Results From First Phase III Trial of Ocrelizumab in Rheumatoid Arthritis
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Phase III Data Showed Rituxan Plus Chemotherapy Improved Survival in Patients With Most Common Form of Adult Leukemia
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Genentech and Biogen Idec Receive a Complete Response from the FDA for Rituxan for Chronic Lymphocytic Leukemia
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Genentech Submits Supplemental Applications to FDA for Avastin Combined with Commonly Used Chemotherapies for Women with Advanced Breast Cancer
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Genentech and Biogen Idec Receive a Complete Response from FDA for Earlier Use of Rituxan for Rheumatoid Arthritis
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Phase III Study Showed Two Years of ACTEMRA ® (tocilizumab) Inhibited Progression of Joint Damage and Improved Disease Remission
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Two Phase III Studies of Lucentis Show Early and Sustained Improvement in Vision in Patients with Retinal Vein Occlusion
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Phase III Study Showed Patients Lived Longer Without Low-Grade Lymphoma Progressing When Rituxan Was Used First-Line for Maintenance
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Avastin Plus Commonly Used Chemotherapies Improved Progression-Free Survival (PFS) in Women with Previously Treated Advanced Breast Cancer
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FDA Approves Avastin for the Most Common Type of Kidney Cancer
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Second Phase III Study Showed Lucentis Improved Vision in Patients with Retinal Vein Occlusion
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Genentech Announces Appointment of Sandra J. Horning, M.D., to Senior Vice President, Global Head, Clinical Development Hematology/Oncology
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Xeloda®-Oxaliplatin Combination (Xelox) Shown to Be More Effective Than Standard Chemotherapy Regimen In Adjuvant Colon Cancer
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New Data from Phase III Saturn Study Showed Tarceva Improved Overall Survival When Used Immediately After Initial Chemotherapy in Patients with Advanced Non-Small Cell Lung Cancer
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Phase III Study Showed Lucentis Improved Vision in Patients with Branch Retinal Vein Occlusion
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Phase III Study Showed Patients Lived Longer Without Advanced Lung Cancer Progressing When Tarceva Was Added to Avastin as First-Line Maintenance Therapy
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Genentech Announces Full Results from First Phase III Study of Avastin in Early-Stage Colon Cancer
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Avastin Plus Commonly Used Chemotherapies Improved Progression-Free Survival in Advanced Breast Cancer
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Genentech and Biogen Idec Submit Applications to the FDA for Rituxan for Most Common Type of Adult Leukemia
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Genentech to Present Advances With Targeted Cancer Medicines at ASCO
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FDA Grants Accelerated Approval of Avastin for Brain Cancer (Glioblastoma) That Has Progressed Following Prior Therapy
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Phase III C-08 Study of Avastin in Early-Stage Colon Cancer Did Not Meet Primary Endpoint
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Genentech Announces Voluntary Withdrawal of Raptiva from the U.S. Market
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FDA Advisory Committee Unanimously Recommends Accelerated Approval of Avastin for Previously Treated Brain Cancer (Glioblastoma)
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Roche Completes Acquisition of Genentech
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OSI Pharmaceuticals Submits Supplemental New Drug Application to the FDA for Tarceva as a First-Line Maintenance Therapy in Advanced Non-Small Cell Lung Cancer
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Roche and Genentech Reach a Friendly Agreement to Combine the Two Organizations and Create a Leader in Healthcare Innovation
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Phase III Study of Rituxan in Lupus Nephritis Did Not Meet Primary Endpoint
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Genentech Urges Stockholders to Take No Action With Respect to Revised Offer From Roche
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Genentech Receives Final Notification Upholding Cabilly Patent in Reexamination Proceeding
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Genentech Announces March 2, 2009 Webcast of Investment Community Meeting
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Genentech Special Committee Rejects Roche's $86.50 Offer as Inadequate
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National Coalition for Cancer Survivorship, UCLA, Wellpoint, and Genentech Launch Initiative to Provide Coordinated Follow-Up Care for People Surviving Cancer
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Genentech Urges Shareholders to Take No Action With Respect to Unsolicited Tender Offer from Roche
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Phase III Study Showed Tarceva in Combination With Avastin as First-Line Maintenance Therapy Improved Progression-Free Survival in Advanced Lung Cancer
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Special Committee of Genentech Board of Directors Responds to Roche's Announced Intention to Commence a Tender Offer
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Genentech Announces Vice President Appointment in Research
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Genentech Announces Full Year And Fourth Quarter 2008 Results
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Genentech Announces January 15 Webcast of Financial and Other Business Results
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Phase III Study Showed Rituxan Decreased The Progression Of Joint Damage In Patients With Early Rheumatoid Arthritis (RA)
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Rituxan in Combination with Chemotherapy Improves Progression-Free Survival in Difficult-to-Treat Form of Blood Cancer
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Avastin Plus Commonly Used Chemotherapies Demonstrated Improved Progression-Free Survival In Advanced Breast Cancer
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Genentech Issues Dear Healthcare Provider Letter Regarding a 2nd Case of PML in a Raptiva Patient
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Phase III Study (SATURN) Showed Tarceva Improved Progression-Free Survival as a First-Line Maintenance Therapy for Advanced Non-Small Cell Lung Cancer
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Genentech Submits Application to U.S. Food and Drug Administration for Avastin in the Most Aggressive Form of Brain Cancer
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Rituxan Data in Patients With Rheumatoid Arthritis To Be Presented at The American College of Rheumatology Annual Scientific Meeting
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Genentech Announces Phase III Study of Avastin Plus Chemotherapy in Adjuvant Colon Cancer Will Continue
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Genentech Announces Third Quarter 2008 Results
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Phase III Study Showed Rituxan in Combination with Chemotherapy Improved Progression-Free Survival in Patients with Relapsed Chronic Lymphocytic Leukemia
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Genentech and OSI Pharmaceuticals Announce Topline Results from Phase III Study Evaluating the Combination of Avastin and Tarceva as Second-Line Treatment for Advanced Non-Small Cell Lung Cancer
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Genentech, Glycart and Roche Enter Into Collaboration Agreement for Potential Cancer Therapy
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Genentech Issues Dear Healthcare Provider Letter Regarding a Reported Case of PML in a Raptiva Patient
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Genentech Announces October 14 Webcast of Financial and Other Business Results
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Genentech Announces Vice President Appointment In Research
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Genentech Special Committee of Independent Directors Responds to Roche Proposal
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Genentech Forms Special Committee of Independent Directors to Review Roche Proposal
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Genentech Announces Receipt of Proposal From Roche
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Genentech Announces Second Quarter 2008 Results
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Genentech Announces July 14 Webcast of Financial and Other Business Results
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Genentech Settles Dispute Related To Cabilly Patent
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Second Phase III Study of Avastin Plus Chemotherapy Shows Improved Progression-Free Survival in Women With Advanced HER2-Negative Breast Cancer
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Genentech Announces June 2 Webcast Discussion of Data Presented at ASCO
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Genentech Provides Update On Studies Of Investigational Biooncology Agents To Be Presented At The American Society Of Clinical Oncology Meeting
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Genentech Provides Update on Avastin Program
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Genentech and Biogen Idec Announce Top-Line Results From Phase II/III Clinical Study of Rituxan in Systemic Lupus Erythematosus
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Genentech Announces Decision In Contract Dispute
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Genentech Provides Update on "AVAiL" Phase III Study of Avastin Plus Chemotherapy in First-Line, Advanced, Non-Squamous, Non-Small Cell Lung Cancer
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Genentech Extends Stock Repurchase Program
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Genentech and Biogen Idec Announce Top-Line Results from a Phase II/III Clinical Trial of Rituxan in Primary-Progressive Multiple Sclerosis
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Genentech Announces First Quarter 2008 Results
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Genentech Announces April 10 Webcast of Financial and Other Business Results
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Genentech Provides Business Update At Annual Investment Community Meeting
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Genentech Announces March 14 Webcast of Investment Community Meeting
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Genentech Receives Notification of Rejection of Cabilly Patent Claims From Reexamination Process
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FDA Grants Accelerated Approval of Avastin in Combination With Paclitaxel Chemotherapy for First-Line Treatment of Advanced HER2-Negative Breast Cancer
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Avado Study of Avastin Plus Docetaxel Chemotherapy Showed Improved Progression-Free Survival in Patients With Advanced Breast Cancer
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Genentech and Biogen Idec Announce Positive Results from a Phase III Trial of Rituxan in Patients With Rheumatoid Arthritis Who Inadequately Responded to Methotrexate
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Genentech Announces Full Year and Fourth Quarter 2007 Results
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Genentech Announces January 14 Webcast Discussion of Financial and Other Business Results
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Genentech Provides Update From Avastin FDA Advisory Meeting
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Genentech Foundation for Biomedical Sciences Awards Nearly $1.2 Million to Health Science Education Programs in the Bay Area
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Avastin Shows Encouraging Results in Phase II Study in Patients With the Most Aggressive Form of Brain Cancer
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Genentech Announces Third Quarter 2007 Results
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Genentech Announces October 15 Webcast Discussion of Earnings and Other Business Results
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Genentech Announces Resubmission of Supplemental Biologics License Application for Avastin in Combination with Paclitaxel for First-Line Metastatic Breast Cancer
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Genentech Announces Expiration of Hart-Scott-Rodino Waiting Period and Completes Acquisition of Tanox
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Genentech Announces Second Quarter 2007 Results
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Abbott and Genentech Announce Global, Integrated Research, Development and Commercialization Collaboration in Oncology
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Genentech Announces July 11 Webcast Discussion of Earnings and Other Business Results
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Updated Overall Survival Data From Pivotal Herceptin Adjuvant Studies in HER2-Positive Breast Cancer
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Genentech Provides Update on Pipeline Agents at The American Society of Clinical Oncology Meeting
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Phase III Study Shows Avastin Plus Interferon Therapy Nearly Doubled Median Progression-Free Survival in Patients with Previously Untreated Advanced Kidney Cancer
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Second Phase III Study of Avastin Plus Chemotherapy Shows Improved Progression-Free Survival in First-Line Non-Squamous, Non-Small Cell Lung Cancer
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Genentech Announces June 4 Webcast Discussion of Data Presented at ASCO
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Rituxan Phase II Data in Patients with Relapsing-Remitting Multiple Sclerosis Presented at the American Academy of Neurology
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Genentech Extends Stock Repurchase Program
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Genentech Announces First Quarter 2007 Results
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Genentech to Provide Business Update at Annual Investment Community Meeting
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Genentech Announces April 11 Webcast Discussion of Earnings and Other Business Results
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Genentech Announces March 23 Webcast of Investment Community Meeting
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Analysis of International Phase III Study of Avastin Plus Chemotherapy Shows Improved Progression-Free Survival in Patients With Advanced Lung Cancer
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Genentech Provides Update on Cabilly Patent Reexamination
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Genentech Announces Additional Effort to Support Patient Access
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Genentech Announces Positive Results from a Phase IV Study of Raptiva in Patients With Moderate-to-Severe Hand and Foot Psoriasis
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Genentech and Tanox Receive "Second Request" from the Federal Trade Commission
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Genentech Announces Senior Vice President and Vice President Promotions in Commercial, Legal and Product Operations
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Genentech Announces Full Year and Fourth Quarter 2006 Results
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Genentech Again Named One of FORTUNE's "100 Best Companies to Work For"
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Genentech and Seattle Genetics Announce Exclusive Global Licensing Agreement for Development and Commercialization of SGN-40
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Genentech Announces Positive Results from a Randomized Phase II Study of Pertuzumab in Combination with Gemcitabine for Advanced Ovarian Cancer
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Genentech Announces January 10 Webcast Discussion of Earnings and Other Business Results
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Key Herceptin Data Presented at San Antonio Breast Cancer Symposium
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New England Journal of Medicine Publishes Data From Pivotal Study of Avastin Plus Chemotherapy in Most Common Type of Lung Cancer
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Interim Analysis of Phase III Trial Shows Avastin Plus Interferon Therapy Improved Progression-Free Survival in Patients With Previously Untreated Advanced Renal Cell Carcinoma
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FDA Approves Herceptin for the Adjuvant Treatment of HER2-Positive Node-Positive Breast Cancer
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Subsequent Course of Rituxan Improved Outcomes in Rheumatoid Arthritis Patients Who Inadequately Responded to TNF Antagonist Therapy
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Genentech Announces Agreement to Acquire Tanox for $20 Per Share
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Genentech Announces Manufacturing Agreements With Lonza
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Genentech Announces Third Quarter 2006 Results
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FDA Approves Avastin in Combination With Chemotherapy for First-Line Treatment of Most Common Type of Lung Cancer
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New England Journal of Medicine Publishes Data From Lucentis Pivotal Phase III Studies in Wet Age-Related Macular Degeneration
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Genentech Announces Vice President Appointments in Commercial Operations and Manufacturing
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Genentech and CGI Pharmaceuticals Enter Into Exclusive Global Strategic Alliance for Potential Products in Multiple Oncology and Autoimmune Indications
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FDA Approves Two New Indications for Rituxan in Patients With Non-Hodgkin's Lymphoma
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Genentech Announces October 10 Webcast Discussion of Third Quarter Earnings and Other Business Results
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Genentech Receives Complete Response Letter From FDA for Avastin in Metastatic Breast Cancer
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Genentech and Biogen Idec Announce Positive Results from a Phase II Trial of Rituxan in Relapsing-Remitting Multiple Sclerosis
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Genentech Foundation for Biomedical Sciences Awards $1.2 Million to Health Science Education Programs in the Bay Area
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Genentech Provides Update On Supplemental Biologics License Application For Adjuvant Herceptin In Early-Stage Her2-Positive Breast Cancer
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Genentech Announces Vice President and Officer Appointments in Product Development and Finance
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Genentech & Inotek Enter into Exclusive Global Strategic Alliance for the Discovery, Development and Commercialization of PARP Inhibitors for Cancer
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Genentech Announces Second Quarter 2006 Results
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Phase III Study of Avastin in Advanced Pancreatic Cancer Does Not Meet Primary Endpoint
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Analysis of Phase III Study Showed Rituxan Plus Methotrexate Reduced Joint Damage in Rheumatoid Arthritis Patients Who Respond Inadequately to TNF Antagonist Therapies
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FDA Approves Avastin in Combination with Chemotherapy for Second-Line Metastatic Colorectal Cancer Patients
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Genentech Announces July 11 Webcast Discussion of Earnings and Other Business Results
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FDA Approves LUCENTIS for the Treatment of Wet Age-Related Macular Degeneration
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Results From a Randomized Phase II Trial Suggested the Combinations of Avastin Plus Tarceva and Avastin Plus Chemotherapy Improved Progression-Free Survival in Advanced Non-Small Cell Lung Cancer
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Preliminary Results from a Phase IIIb Study Showed Patients with Wet AMD Treated with Lucentis Quarterly Experienced a 16-Letter Benefit over the Control Group at One Year
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Genentech Submits Supplemental Biologics License Application for Avastin with Chemotherapy in First-Line Metastatic Breast Cancer
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Genentech Announces June 5 Webcast Discussion of Data Presented at ASCO
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Recruitment to Resume in Avastin International Phase III Trial (AVANT) in Early-Stage Colon Cancer
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Genentech Announces June 2 Webcast Discussion Of Lucentis Data Presented At The 2006 Retinal Physician Symposium
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Genentech Announces Vice President Appointments In Commercial Operations And Product Development
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Genentech Extends Stock Repurchase Program
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Genentech Submits Supplemental Biologics License Application for Avastin with Chemotherapy in First-Line, Non-Squamous, Non-Small Cell Lung Cancer
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Genentech Announces First Quarter 2006 Results
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Genentech Announces Vice President Appointments in Commercial Operations and Product Development
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Genentech and Biogen Idec Submit Supplemental Biologics License Application for First-Line Use of Rituxan in Low-Grade or Follicular CD20-Positive B-Cell Non-Hodgkin's Lymphoma
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Genentech Announces April 11 Webcast Discussion of Earnings and Other Business Results
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Genentech Provides Updates at Annual Investment Meeting
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Genentech Announces March 17 Webcast of Investment Community Meeting
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Genentech Granted Six-Month Priority Review for Lucentis for the Treatment of Wet Age-Related Macular Degeneration
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FDA Approves Rituxan - The First Targeted B-Cell Therapy for Treatment of Moderate-to-Severe Rheumatoid Arthritis
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Genentech Submits Supplemental Biologics License Application for Adjuvant Herceptin in Early-Stage HER2-Positive Breast Cancer
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Recruitment Temporarily Suspended in an International Phase III Trial (AVANT) in Early-Stage Colon Cancer
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FDA Approves Rituxan Plus CHOP or other Anthracycline-Based Chemotherapy Regimens for First-Line Treatment of Diffuse Large B-Cell Non-Hodgkin's Lymphoma
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Amgen and Genentech Sign License Agreements for Antibody Patents
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Preliminary Phase III Data from Head-to-Head Study of Lucentis Shows Lucentis Improved Vision Compared to Visudyne in Patients with Wet Age-Related Macular Degeneration
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Genentech Announces Full Year and Fourth Quarter 2005 Results
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Genentech Named Number 1 on FORTUNE's 100 Best Companies to Work For
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Genentech Announces Vice President Appointments in Commercial Operations, Corporate Information Technology, Product Development and Product Operations
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Genentech Announces January 14th Webcast Discussion Of Data Presented At Macula 2006 Meeting
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Genentech Announces Executive Promotions
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Genentech Announces January 10 Webcast Discussion of Earnings and Other Business Results
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Genentech Submits Biologics License Application for FDA Review of Lucentis in Wet Age-Related Macular Degeneration
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Genentech Submits Supplemental Biologics License Application for Avastin in Relapsed Metastatic Colorectal Cancer
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Biogen Idec and Genentech Announce November 16th Webcast Discussion of Rituxan Data Presented at ACR
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Preliminary Data from Phase III Trial Show Lucentis is the First Investigational Therapy to Demonstrate Clinical Benefit over Visudyne in a Head-to-Head Study of Patients with Wet AMD
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FDA Approves Tarceva in Combination with Gemcitabine Chemotherapy for Treatment of Locally Advanced, Inoperable or Metastatic Pancreatic Cancer
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Biogen Idec and Genentech Announce FDA Acceptance of Supplemental Biologics License Application and Priority Review Designation for Rituxan in Rheumatoid Arthritis
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FDA Grants Priorty Review for Rituxan Supplemental Biologics License Application for Front-Line Treatment of Intermediate-Grade or Aggressive Non-Hodgkin's Lymphoma
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Genentech and ABC2 Announce Second Brain Cancer Collaboration
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Pivotal Herceptin Data in the New England Journal of Medicine Showed Significant Improvement in Disease-Free Survival in Early-Stage HER2-Positive Breast Cancer
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Genentech Announces Preliminary Results from Randomized Phase II Trial of Avastin and Tarceva in Kidney Cancer
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Genentech Announces Third Quarter 2005 Results
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Genentech Provides Information on Patent Reexamination
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Genentech Provides Update on Phase II Study with Avastin in Platinum-Refractory Ovarian Cancer
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Genentech Announces October 10 Webcast Discussion of Earnings and Other Business Results
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FDA Advisory Panel Recommends Tarceva Approval for Pancreatic Cancer
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Fourth Phase III Study Shows Herceptin Plus Chemotherapy Improved Disease-Free Survival in Early-Stage HER2-Positive Breast Cancer
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Genentech Announces Plans to File for FDA Approval of Lucentis for the Treatment of Wet Age-Related Macular Degeneration in December
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Biogen Idec and Genentech Submit a Supplemental Biologics License Application for FDA Review of Rituxan for the Treatment of Rheumatoid Arthritis
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Genentech and Biogen Idec File Supplemental Biologics License Application for FDA Review of Rituxan for Front-Line Treatment of Intermediate Grade or Aggressive CD-20-Positive, B-Cell, Non-Hodgkin's Lymphoma
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Genentech Announces Organizational Changes
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Genentech Foundation for Biomedical Sciences Bolsters Innovation in Health Science Education with $1.2 Million for Bay Area Programs
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Preliminary Phase I/II Study Showed Lucentis Improved Vision in Patients with Wet Age-Related Macular Degeneration When Used in Combination with Visudyne
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Phase III Study Shows Lucentis Improved Vision in Patients With Wet Age-Related Macular Degeneration
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Pivotal Phase III Tarceva Study Published in the New England Journal of Medicine Showed Survival Improvement in Advanced Non-Small Cell Lung Cancer
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Genentech Announces Pricing of $2 Billion in Senior Notes
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Genentech Announces Intention to Offer up to $2 Billion in Senior Notes
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Genentech Announces Second Quarter 2005 Results
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Genentech Announces July 18 Webcast Discussion of Data Presented at ASRS
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Genentech Announces Vice President Appointments in Product Operations, Regulatory, and Research
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Genentech Provides Manufacturing Update
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Genentech Announces June 24 Webcast Discussion of Recent Manufacturing Activities
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Genentech Announces July 11 Webcast Discussion of Earnings and Other Business Results
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Biologics Manufacturing Facility to be Purchased by Genentech from Biogen Idec
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Genentech Extends Share Repurchase Program
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Preliminary Phase IIb Study Showed Rituxan Improved Symptoms in Rheumatoid Arthritis Patients Who Failed One or More Disease-Modifying Anti-Rheumatic Drugs
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Preliminary Phase I/II Data Show Lucentis in Combination With Visudyne Maintained or Improved Vision in Approximately 90 Percent of Patients With Wet Age-Related Macular Degeneration
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Preliminary Phase III Data Show Lucentis Maintained or Improved Vision in Nearly 95 Percent of Patients with Wet Age-Related Macular Degeneration
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Data From Omnitarg Clinical Program Presented at American Society of Clinical Oncology Meeting
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Phase III Study of Tarceva in Combination with Chemotherapy Improves Survival in Pancreatic Cancer Patients
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Herceptin Plus Chemotherapy Improved Disease-Free Survival and Overall Survival in Adjuvant Setting for Early-Stage Her2-Positive Breast Cancer Patients
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Avastin Plus Chemotherapy Showed Doubling of Time Without Cancer Progression in Phase III Trial of
First-Line Metastatic Breast Cancer Patients
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Phase III Trial of Avastin Plus Chemotherapy Showed 30 Percent Improvement in Overall Survival in First-Line Non-Squamous, Non-Small Cell Lung Cancer
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Genentech Announces Webcast Discussions of Data Presented at ASCO; Phase III Breast Cancer Studies to be Presented at Educational Session
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Genentech Announces Vice President Appointments in Product Operations and Product Development
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OSI Pharmaceuticals and Genentech Announce Filing of a Supplemental New Drug Application to the FDA for Tarceva in Pancreatic Cancer
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Interim Analysis of Phase III Studies Shows Herceptin Plus Chemotherapy Improves Disease-Free Survival in the Adjuvant Setting for Early-Stage HER2-Positive Breast Cancer Patients
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Interim Analysis of Phase III Trial Shows Avastin Plus Chemotherapy Improved Progression-Free Survival in Patients with First-Line Metastatic Breast Cancer
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Genentech Announces First Quarter 2005 Results
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Phase III Study Shows Rituxan Significantly Improves Symptoms in Patients with Rheumatoid Arthritis Who Inadequately Responded to Anti-TNF Therapies
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Genentech Announces April 11 Webcast Discussion of Earnings and Other Business Results
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Genentech and Ipsen Agree to Develop Sustained-Release Formulations of Recombinant Human Growth Hormone
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Interim Analysis of Phase III Trial Shows Avastin Plus Chemotherapy Extends Survival of Patients with First-Line Non-Squamous, Non-Small Cell Lung Cancer
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Genentech Announces Strategic Updates at Investment Meeting
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Genentech Announces March 4 Webcast of Investment Community Meeting
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Three-Year Study with Raptiva Showed Long-Term and Sustained Clearing in Moderate-to-Severe Plaque Psoriasis Patients
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Data From Phase III Study Show Tarceva Plus Gemcitabine Significantly Improves Survival Compared to Gemcitabine Alone in Advanced Pancreatic Cancer Patients
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Preliminary Positive Results from Phase III Trial of Avastin Plus FOLFOX4 Chemotherapy Presented at ASCO GI Meeting
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Genentech Announces Fourth Quarter and Full Year 2004 Results
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Genentech Again Named One of FORTUNE's "100 Best Companies To Work For"
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Genentech Finalizes Avastin Label with Previously Announced Safety Information
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Genentech Board Announces Executive Promotions and Senior Appointments in Commercial Operations, Finance and Manufacturing
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Genentech Announces January 10 Webcast Discussion of Earnings and Other Business Results
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Phase III Results Show Avastin Plus Folfox4 Chemotherapy Significantly Extend Survival in Second-Line Metastatic Colorectal Cancer
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Genentech Again Named the No. 1 Employer in Science Magazine Survey
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Genentech Announces November 18 Webcast Discussion of Tarceva FDA Approval
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FDA Approves Tarceva for Patients with Advanced Non-Small Cell Lung Cancer
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Genentech Announces Organizational Changes
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Genentech and Rinat Neuroscience Announce Co-Development and Joint Commercialization Agreement for Anti-NGF Antibody for Acute and Chronic Pain
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Genentech Announces Senior Appointments in Manufacturing and Engineering
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Preliminary Phase IIb Data Show Rituxan Improved Symptoms in Patients with Moderate-to-Severe Rheumatoid Arthritis
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Genentech to Seek Review of Court Decision in Contract Dispute
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Genentech Announces Third Quarter 2004 Results
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Genentech Receives Subpoena on Rituxan
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Genentech Extends Share Repurchase Program
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Genentech and Wyeth Announce Manufacturing Agreement
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Tarceva Plus Gemcitabine Improves Survival Compared to Gemcitabine Alone in First-Line Pancreatic Cancer Patients
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Genentech Announces October 6 Webcast Discussion of Earnings and Other Business Results
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Genentech and OSI Pharmaceuticals Initiate Phase IIIB Clinical Trial of Tarceva in Advanced Non-Small Cell Lung Cancer
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Giants and Genentech Devote Sunday, September 5 to Striking Out Cancer
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Genentech Announces FDA Approval of Avastin Manufacturing at Vacaville Facility
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OSI Pharmaceuticals and Genentech Announce Completion of New Drug Application for FDA Approval of Tarceva
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Preliminary Data Showed Sustained Clinical Benefit for Moderate-to-Severe Plaque Psoriasis Patients Treated with Raptiva for 30 Months
|
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Genentech Announces Second Quarter 2004 Results
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Genentech Announces Senior Appointments in Commercial Operations and Development
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Genentech Announces July 7 Webcast Discussion of Earnings and Other Business Results
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Positive Data from Preliminary Phase II Study of Rituxan in Rheumatoid Arthritis Published in the New England Journal Of Medicine
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OSI Pharmaceuticals and Genentech Enter into Co-Promotion and Manufacturing Agreements for Tarceva
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Phase III Study of Tarceva in Relapsed Non-Small Cell Lung Cancer Shows Significant Improvement in Survival
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Genentech Presents Data from Broad Avastin Clinical Trial Program at the American Society of Clinical Oncology Meeting
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Key Herceptin Data Presented at American Society of Clinical Oncology Meeting
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Early Clinical Data Evaluating the Combination of Avastin and Tarceva Yield Initial Promising Results in Several Cancers
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Preliminary Results of a Phase III Study Showed Rituxan Maintenance Therapy Improved Progression-Free Survival in Newly Diagnosed Patients with Indolent Non-Hodgkin's Lymphoma
|
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Preliminary Phase III Data Showed Front-Line Use of Rituxan Plus Chemotherapy Improved Survival in Patients Under 60 with Aggressive Non-Hodgkin's Lymphoma
|
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Pivotal Avastin Study in New England Journal of Medicine Showed Significant Improvement in Patients with Metastatic Colorectal Cancer
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Genentech and Alkermes Announce Decision to Discontinue Commercialization of Nutropin Depot
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Genentech Announces Webcast Discussions of Data Presented at ASCO
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Genentech Foundation for Biomedical Sciences Awards More Than $1 Million to Science Education Programs in the Bay Area
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Tarceva Extends Survival of Patients with Relapsed Non-Small Cell Lung Cancer
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Genentech Announces Approval of Two-for-One Stock Split
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Genentech Announces First Quarter 2004 Results - Increase of 28 Percent in Product Sales
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Genentech Win in Chiron Patent Litigation Unanimously Affirmed by U.S. Court of Appeals
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Genentech Announces Senior Appointment in Corporate Information Technology
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Genentech and XOMA Announce Results of Phase II Study of Raptiva in Psoriatic Arthritis Patients
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Genentech Announces Long-Term Strategy and Financial Goals
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Genentech Announces April 7 Webcast Discussion of Earnings and Other Business Results
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Genentech Announces Organizational Changes
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Genentech's Board of Directors Approves a Conditional Stock Split
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Genentech Announces March 12 Webcast of Investment Community Meeting
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FDA Approves Avastin, a Targeted Therapy for First-Line Metastatic Colorectal Cancer Patients
|
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Genentech, Novartis and Tanox Settle Disputes Surrounding Xolair and TNX-901
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Genentech Announces Senior Appointments in Development, Commercial and Manufacturing
|
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Genentech Reports $3.3 Billion in Revenues with $1.9 Billion in Oncology Sales
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Genentech Announces Webcast of Presentation at JP Morgan 22nd Annual Healthcare Conference
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Genentech Named Number 15 on Fortune's "Best Companies To Work For" List
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Genentech and Lonza Announce Manufacturing Agreement
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Genentech Announces January 14 Webcast Discussion of Earnings and Other Business Results
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Phase III Trial of Rituxan Plus Chemotherapy as a Front-Line Therapy in Aggressive Non-Hodgkin's Lymphoma Reaches Pre-Specified Efficacy Endpoint Two Years Early
|
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Initial Results of a Randomized Phase II Study Suggest that Rituxan Maintenance Therapy Prolongs Remission in Indolent NHL
|
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Initial Results of a New Study of Rituxan Plus CVP Chemotherapy Demonstrate Prolonged Time to Treatment Failure as Front-Line Therapy for Patients with Indolent Non-Hodgkin's Lymphoma
|
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Initial Data from Phase III ECOG 4494 Study of Rituxan as Front-Line and Maintenance Therapy in Aggressive Non-Hodgkin's Lymphoma (NHL) Presented at ASH
|
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Genentech Announces Share Repurchase Program
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Preliminary Results of a Phase II Study of Herceptin and Taxotere (docetaxel) Combination Suggests Improved Survival in HER2-Positive Metastatic Breast Cancer Patients
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Genentech Announces FDA Acceptance of Biologics License Application with Priority Review of Avastin In First-Line Metastatic Colorectal Cancer
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Genentech Announces December 7th Webcast Discussion of Data Presented at ASH
|
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Genentech Reports Results from Phase II Trial of Avastin in Metastatic Colorectal Cancer
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Study in New England Journal of Medicine Shows Extending Raptiva (efalizumab) Treatment Provides Rapid and Continuous Benefit
|
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Eastern Cooperative Oncology Group (ECOG) Phase III Trial of Rituxan Maintenance Therapy in Indolent Non-Hodgkin's Lymphoma Reaches Pre-Specified Efficacy Endpoint Early
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Boehringer Ingelheim and Genentech Announce Initiation of a Clinical Trial Evaluating TNKase/Metalyse Use Prior to Angioplasty for Treatment of Heart Attack
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Genentech Named to "Scientific American 50" List
|
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Initial Data Released From Phase III ECOG 4494 Study of Rituxan as Front-Line and Maintenance Therapy in Aggressive Non-Hodgkin's Lymphoma
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Follow-Up Data from Phase II Study of Rituxan as a Potential Treatment for Rheumatoid Arthritis Show Durability of Response at 48 Weeks
|
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Genentech Named the No. 1 Rated Employer in Science Magazine Survey
|
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FDA Approves Raptiva (efalizumab) for Chronic Moderate-to-Severe Plaque Psoriasis
|
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Genentech Reports 17 Percent Increase in Non-GAAP Earnings Per Share for Third Quarter 2003
|
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Genentech Announces Senior Appointments in Commercial Operations and Research
|
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Phase III Trials of Tarceva(TM) Plus Chemotherapy in First-Line Non-Small Cell Lung Cancer Do Not Meet Primary Efficacy Endpoint
|
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Genentech Files Biologics License Application for FDA Approval of Avastin in First-Line Metastatic Colorectal Cancer
|
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Genentech Announces October 8 Webcast Discussion of Earnings and Other Business Results
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FDA Advisory Committee Unanimously Recommends Approval for Raptiva as a Potential Treatment for Moderate-to-Severe Plaque Psoriasis
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Genentech Promotes Richard Scheller to Executive Vice President, Research
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Genentech Appoints Marc Tessier-Lavigne to Senior Vice President, Research Drug Discovery
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Genentech Announces September 9th Webcast Discussion of DODAC Review of Raptiva BLA
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Genentech and Amgen Settle Patent Dispute
|
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|
Genentech Presents Positive Preliminary Six-Month Data from Phase Ib/II Study for Lucentis in Age-Related Macular Degeneration (AMD)
|
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|
Tarceva (erlotinib HCl) Phase II Clinical Trial Initiated in Patients with Malignant Glioma
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Genentech and XOMA Announce FDA Advisory Committee Review of Raptiva
|
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New Data Support Raptiva as a Potential Long-Term Treatment for Moderate-to-Severe Plaque Psoriasis
|
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Genentech Announces Senior Appointments in Research and Commercial Operations
|
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Genentech Reports 35 Percent Increase in Non-GAAP Earnings Per Share for Second Quarter
|
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Genentech Receives FDA Fast-Track Designation for Avastin
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Genentech Announces July 9 Webcast Discussion of Earnings and Other Business Results
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Genentech and Novartis Ophthalmics Announce Development and Commercialization Agreement for Age-Related Macular Degeneration Treatment, Lucentis
|
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Genentech and IDEC Announce Humanized Anti-CD20 Antibody Development Collaboration
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FDA Approves Xolair, Biotechnology Breakthrough for Asthma
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Genentech and Biogen Announce Autoimmune Collaboration
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Positive Results from Phase III Avastin Study in Metastatic Colorectal Cancer Presented at ASCO
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Clinical Data from Phase II Study in Early Breast Cancer Suggest Potential Use of Herceptin with New Chemotherapy Combination
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Genentech Reports Additional Data from BioOncology Pipeline at ASCO
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Tarceva (erlotinib HCl) Shows Encouraging Safety Profile and Activity in Phase I Clinical Study in Patients with Malignant Glioma
|
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Preliminary Positive Data From Rituxan Multi-Center Trial in First-Line and Maintenance Therapy in Patients with Chronic Lymphocytic Leukemia (CLL)
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Genentech Names Corsee Sanders Vice President, Biometrics and Business Operations, Medical Affairs
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Genentech Announces June 1st Webcast Discussion of Data Presented at ASCO
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Phase III Trial of Avastin Plus Chemotherapy Markedly Extends Survival of Metastatic Colorectal Cancer Patients
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|
FDA Advisory Committee Unanimously Recommends Approval of Xolair
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Genentech and XOMA Discontinue Rheumatoid Arthritis Trial
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Genentech Announces May 15th Webcast Discussion of PADAC Review of Xolair BLA
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Genentech And ABC(2) Agree to Collaborate on Brain Cancer Clinical Trial
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Genentech Announces April 23 Webcast of Annual Meeting of Stockholders
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Genentech Foundation for Biomedical Sciences Awards $1 Million to Science Education Programs in the Bay Area
|
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Genentech Reports 59 Percent Increase in Non-GAAP Earnings Per Share for First Quarter
|
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Genentech Announces April 9 Webcast Discussion of Earnings and Other Business Results
|
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Genentech, Novartis and Tanox Announce FDA Advisory Committee Review of Xolair (Omalizumab)
|
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Preliminary Results from Open-Label Raptiva Study Suggest Continued Benefit with Long-Term Treatment
|
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Phase III Study Results with Raptiva in the Treatment of Psoriasis Presented at Annual AAD Meeting
|
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Genentech Projects Double-Digit Growth for 2005-2010
|
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Genentech Appoints Philippa Norman Vice President, Global Supply Chain
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Genentech Announces March 21 Webcast Discussion of Data Presented at the American Academy of Dermatology
|
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Genentech Announces March 14 Webcast of Investment Community Meeting
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Genentech Appoints Ian Clark Senior Vice President and General Manager, BioOncology
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Genentech Exceeds $2.7 Billion in Revenues with $1.5 Billion in Oncology Sales
|
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Genentech Announces Webcast of Presentation at JP Morgan 21st Annual Healthcare Conference
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Genentech Named One of Fortune's "100 Best Companies To Work For"
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Genentech Announces January 15 Webcast Discussion of Earnings and Other Business Results
|
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Genentech and XOMA Submit Biologics License Application for FDA Approval of Raptiva(TM) (Efalizumab) for the Treatment of Moderate-to-Severe Plaque Psoriasis
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Genentech and Novartis Submit Amendment to the Biologics License Application for Xolair (TM) (Omalizumab) to FDA
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Preliminary Results from Phase III Study Demonstrate Herceptin/Chemotherapy Combination Delays Time to Disease Progression in HER2-Positive Breast Cancer
|
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Investigational Data Demonstrate Potential of Extended Rituxan(R) Use to Increase Event-Free Survival in Patients with Indolent NHL
|
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Pre-Hospital Thrombolytic Treatment of Heart Attack Found Feasible and Faster Than In-Hospital Therapy
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Preliminary Positive Data from Investigational Randomized Phase II Trial Demonstrates Rituxan as a Potential Treatment for Rheumatoid Arthritis
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Genentech Reports 23 Percent Increase in Product Sales for Third Quarter
|
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Genentech Reports First Quarter Results
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Genentech Announces Senior Appointments in Medical Affairs and Research
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Genentech Announces Preliminary Positive Phase Ib/II Data for rhuFab V2 in Age-Related Macular Degeneration (AMD)
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Genentech Announces October 9 Webcast Discussion of Earnings and Other Business Results
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Genentech Recognized as One of The 100 Best Companies for Working Mothers
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Genentech Listed as Top Employer in Science Survey
|
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Genentech and XOMA Announce Phase III Study with Raptiva(TM) Achieves Primary Efficacy Endpoint
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Phase III Trial With Avastin(TM) in Relapsed Metastatic Breast Cancer Does Not Meet Primary Endpoint
|
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Genentech Wins Patent Dispute With Chiron
|
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Genentech Names Stephen G. Juelsgaard Executive Vice President
|
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Genentech Receives FDA Approval to Include HER2 Gene Detection Test in Herceptin(R) Product Labeling
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OSI Pharmaceuticals and Genentech Provide Update on Status of Tarceva Program
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Genentech Extends Stock Repurchase Program
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U.S. PTO Interference Declared in Genentech/Chiron Patent Dispute
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Serono and Genentech Announce International Marketing Agreement for Psoriasis Treatment Raptiva
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Tarceva U.S. Phase III Non-Small Cell Lung Cancer Clinical Trial Completes Patient Enrollment
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Genentech and XOMA Announce Preliminary Data from Long-Term Study with Investigational Psoriasis Therapy
|
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Genentech Reports 28 Percent Increase in Product Sales for Second Quarter
|
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Genentech Announces July 10 Webcast Discussion of Earnings and Other Business Results
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Genentech to Appeal Judgment in Contract Dispute
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Preliminary Data from Phase II Study of Rituxan for Rheumatoid Arthritis are Positive
|
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Investigational Data from Randomized Study of Extended Therapy with Rituxan(R) Demonstrates Potential to Delay Disease Progression in Patients with Indolent NHL
|
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Genentech Announces Verdict in Contract Dispute
|
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Investigational Data Demonstrates Potential Use of Rituxan in Various CD20-Positive Cancers
|
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National Cancer Institute (NCI) Study Demonstrates Genentech's Investigational Anti-Angiogenesis Treatment Avastin(TM) Delays Time to Disease Progression in Metastatic Kidney Cancer
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Genentech Appoints Hal Barron Vice President, Medical Affairs
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Genentech and OSI Pharmaceuticals Announce FDA Fast-Track Designation for Tarceva(tm)
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Genentech Invites Investors to Listen to Webcast of May 21 Discussion of ASCO Presentations
|
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FDA Approves Nutropin AQ PEN (TM) For Delivery Of Nutropin AQ (R) Recombinant Growth Hormone
|
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Genentech Foundation for Biomedical Sciences Awards $869,411 to Support Quality Science Education in the Bay Area
|
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Genentech Reports 22 Percent Increase in Product Sales For First Quarter
|
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Genentech and Xoma Obtain Results from Xanelim(TM) (Efalizumab) Pharmacokinetic Study
|
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Genentech Announces April 9 Webcast Discussion of Earnings and Other Business Results
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Phase III Trial with Anti-IgE Shows Positive Results in Treating Seasonal Allergic Rhinitis
|
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Follow-Up Data Shows Improvement in Overall Survival in Metastatic Breast Cancer Patients Treated with Herceptin, Plus Chemotherapy
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Genentech Confirms Growth Hormone Research Performed Independently; Seeburg Testimony is False
|
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Immunex Corporation and Genentech, Inc. Join Forces To Develop TRAIL/Apo2L in Cancer
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No Verdict Reached in Genentech, University of California Patent Infringement Case
|
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Genentech to Remain Independent Company, Roche Intends to Exercise Its Call Option and Publicly Reissue Genentech Shares
|
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Study Shows Simpler Procedures Employed by Industry-Sponsored Heart Attack Registry Are Comparable to More Complex Government Program
|
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Genentech and Immunex Announce Patent License Agreement for Immunoadhesin Technology for ENBREL
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Phase III Clinical Trial Shows Promising Results of Nutropin Depot
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SEC Registration Filed for Genentech Public Offering
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Roche Exercises Option to Redeem Genentech Shares
|
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Genentech and Alkermes Announce the Submission of a New Drug Application with the FDA for Nutropin Depot
|
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Genentech Scientists Receive Distinguished Inventor Award
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Genentech Appoints Diane Parks Vice President of Marketing
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Unique Program Allows Previous Genentech Shareholders to be Included in Genentech Public Offering
|
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Genentech Submits Application for FDA Approval of Tenecteplase (TNK-tPA)
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XOMA Announces Expansion of Genentech Collaboration in hu1124 to Include Organ Transplant Rejection
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Genentech Appoints Laura Leber Vice President, Corporate Communications
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Genentech Appoints James Panek, Senior Vice President, Product Operations
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Genentech Named Among 100 Best Companies For Working Mothers
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Genentech Launches Annual Program to Boost Economic Development of Its Hometown of 23 Years
|
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Genentech Names Levinson as New Board Chair and Announces Appointment of Two New Directors
|
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Genentech Appoints Sulzbach Vice President, Information Resources
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Genentech Chairman/CEO Arthur Levinson Receives Irvington Institute's Corporate Leadership Award
|
|
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Roche To Publicly Sell 20 Million Genentech Shares, Genentech Board Approves 2-For-1 Stock Split
|
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SEC Registration Filed for Genentech Public Offering
|
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Secondary Offering by Roche of 20 Million Genentech Shares Priced at $143.50
|
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Genentech 2-For-1 Stock Split Effective on October 29
|
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Genentech and Chairman/CEO Levinson to Receive National Breast Cancer Coalition's Corporate Leadership Award
|
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Genentech and IDEC Pharmaceuticals to Receive 1999 Trailblazers Award from Cure for Lymphoma Foundation
|
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COR Therapeutics, Schering-Plough and Genentech Announce Plans to Study INTEGRILIN -- eptifibatide -- Injection in Combination with TNKase -- tenecteplase -- in Heart Attack Patients
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University of California and Genentech Settle Patent Infringement Lawsuits
|
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FDA Approves Efficacy Results for Spine Bone Mineral Density in Childhood-Onset Growth Hormone Deficient Adults
|
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New Data from Key Rituxan Clinical Studies Presented at 41st Annual Society of Hematology Meeting
|
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Genentech to Proceed With Phase III Trials of Experimental Anti-Angiogenesis Monoclonal Antibody
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Phase III Anti-IgE Asthma Clinical Trials Show Positive Preliminary Results
|
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Genentech Named One of Fortune's "100 Best Companies to Work for in America"
|
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Genentech and XOMA Announce Initiation of Anti-CD11A Phase III Clinical Trials for Psoriasis
|
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Genentech and Inspire to Collaborate on Respiratory Therapeutics
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FDA Approves Nutropin Depot(TM), First Long-Acting Dosage Form of Recombinant Growth Hormone for Growth Hormone Deficiency in Children
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Genentech Issued New t-PA Patent and Files Patent Infringement Suit Against Centocor's Thrombolytic Agent
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Preliminary Phase II Trial Results with Experimental Vascular Endothelial Growth Factor in Patients with Coronary Artery Disease are Disappointing
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Genentech Names Ebersman Vice President
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Phase III Trial With Nerve Growth Factor Did Not Reach Its Goal
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International Trial Shows Promising Results for Genentech's New Clot Buster Compared with Activase
|
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Genentech Discussing Settlement with U.S. Government
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Genentech Reports 1999 First Quarter Results
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Genentech Confirms Settlement Agreement with U.S. Government
|
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XOMA and Genentech Extend hu1124 (Anti-CD11a) Collaboration Through Phase III
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Genentech Reports 1999 Second Quarter Results
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Genentech, Inc. Announces Public Offering of 20 Million Shares Under New NYSE Trading Symbol, DNA
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Genentech Names Gene Murano Vice President, Regulatory Affairs
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Genentech Corporate Child Care Center Celebrates 10 Years
|
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Genentech Reports 41 Percent Increase in Year-End Net Income
|
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Schwarz Pharma AG and Genentech enter into a collaboration for two growth hormone products
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Roche and GNE Announce Agreement for Roferon-A
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Genentech Reports 1996 Year-End Results
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Genentech Appoints Two New Vice Presidents
|
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Comparison of Two Heart Attack Drugs Fails to Prove Primary Endpoint
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Leader in Oncology to Head Genentech's Molecular Oncology Department
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Bill Young Appointed COO of Genentech
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FDA Clears Genentech's Nutropin AQ
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Scios Suspends Development of AURICULIN
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Genentech is Granted Patents for Recombinant Factor VIII
|
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Genentech Reports 1997 First Quarter Results
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IDEC, Genentech & Roche Submit Applications for Approval of IDEC-C2B8
|
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Genentech Focuses On Cancer as it Launches BioOncology Initiative
|
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Genentech Announces Plans to Study TNK-tPA in Phase III
|
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Genentech Appoints Lars Barfod Vice President of Marketing
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Genentech and South San Francisco Celebrate Community Program
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Genentech Creates New Strand of DNA
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Genentech Reports 1997 Second Quarter Results
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FDA Advisory Committee Recommends Clearance for Cancer Treatment
|
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|
New Clot-Dissolving Agent Shows Promise
|
|
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Health Care Pioneers Reinforce Commitment to Improving Public Health
|
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Genentech Discontinues IGF-I Drug Development Effort in Diabetes
|
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Anti-IgE Monoclonal Antibody Progresses to Phase III Trials in Asthma
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Genentech Reports 1997 Third Quarter Results
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Genentech and Alkermes Announce Plans to Advance Prolease®, Human Growth Hormone to Phase III Clinical Trials
|
|
|
First New Drug for Non-Hodgkin's Lymphoma in Decade Receives FDA Clearance for Marketing
|
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|
Alteon and Genentech to Collaborate on Therapy for Diabetic Complications
|
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Genentech Wins Clearance of Nutropin for Growth Hormone Deficiency
|
|
|
New Drug for Non-Hodgkin's Lymphoma Available Now
|
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LeukoSite and Genentech Enter Collaboration
|
|
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Genentech Announces Phase III Investigational Trial Results
|
|
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Genentech Wins FDA Clearance of its Ready-To-Use Nutropin AQ
|
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|
FDA Grants Genentech Clearance to Market Nutropin AQ
|
|
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Levinson Appoints McLaughlin and Young as Executive Vice Presidents
|
|
|
Genentech Posts Strong Year-End Results
|
|
|
Genentech Announces Creation of Genenvax to Develop AIDS Vaccine
|
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|
Genentech Names Cynthia Ladd VP, Corporate Law
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Genentech Submits Product License Application for Activase
|
|
|
Genentech Licenses Worldwide Rights From Washington University for GDNF Homologue, Neurturin
|
|
|
Biotechnology Pioneer Genentech Turns 20
|
|
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Genentech Wins Second Major Biotechnology Patent Dispute In Japan
|
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Appeals Court Upholds Preliminary Injunction Prohibiting Sales of Biotechnology General's Growth Hormone Product
|
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|
Genentech Reports 1996 First Quarter Results
|
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|
Genentech and XOMA Agree to Develop Jointly Anti-CD11a
|
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|
Genentech Names Henner as Head of Research
|
|
|
Genentech Names Robert Arathoon to VP of Process Science
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Genentech Donates $25,000 To Solano Community College
|
|
|
Activase Cleared by FDA for U.S. Marketing
|
|
|
Genentech Granted Preliminary Injunction
|
|
|
Tanox Biosystems and Genentech Settle Lawsuits
|
|
|
Genentech Reports 1996 Second Quarter Results
|
|
|
Genentech Employees Take Another $50,000 Shopping Spree In Downtown South San Francisco, The Company's Hometown For 20 Years
|
|
|
Delaware Court Approves Settlement
|
|
|
Genentech Files Amended Complaint Against Novo Nordisk
|
|
|
Patent Infringement Suit Filed Against Boehringer
|
|
|
FDA Advisory Committee Recommends Pulmozyme
|
|
|
Genentech Advances Study of Nerve Growth Factor
|
|
|
FDA Advisory Committee Recommends Approval of Activase
|
|
|
Genentech Reports 1996 Third Quarter Results
|
|
|
Genentech Discontinues Pursuit of Actimmune for Renal Cell Carcinoma
|
|
|
New Senior Vice Presidents
|
|
|
Pulmozyme Receives Marketing Clearance for Use in Advanced Cystic Fibrosis Patients
|
|
|
Genentech and Baxter to Collaborate
|
|
|
IDEC Pharmaceuticals and Genentech Announce Positive Final Results
|
|
|
Genentech Founder Swanson Retires as Board Chair
|
|
|
Genentech Names Dick Munro as New Board Chair
|
|
|
FDA Clears Genentech's Nutropin Human Growth Hormone
|
|
|
FDA Advisory Committee Recommends Nutropin
|
|
|
Genentech Board Names Levinson President & CEO
|
|
|
Pharmacia & Upjohn Acquires Rights from Genentech for Thrombopoietin (TPO)
|
|
|
Sumitomo Pharmaceuticals and Genentech Enter Into Collaboration
|
|
|
Genentech's Year-End Results On Track
|
|
|
Vice President Gore To Visit Genentech
|
|
|
Genentech and Dako Announce Collaboration on HER2 Diagnostic Kit In Breast Cancer
|
|
|
Genentech Files Patent Infringement Suit Against Centocor's Thrombolytic Agent
|
|
|
Genentech Receives Fast Track Product Designation for Herceptin By FDA
|
|
|
Genentech Names Moore New Head of Government Affairs Office
|
|
|
Genentech Reports 1998 First Quarter Results - 30 Percent Earnings Increase
|
|
|
Genentech Submits Application for FDA Approval of HER2 Antibody, Herceptin
|
|
|
Genentech Names Dennis Henner and Stephen Juelsgaard to Senior Vice Presidents
|
|
|
Results of Phase III Studies Announced for HER2 Antibody, Herceptin
|
|
|
Genentech Names Moore Vice President of Government Affairs
|
|
|
Phase II Pilot Study of Rituxan with Chemotherapy Showed 97% Response Rate in Type of Non-Hodgkin's Lymphoma
|
|
|
Genentech Names Johnston Vice President, Intellectual Property
|
|
|
Novo Nordisk and Genentech Settle Long Term Dispute over Patents
|
|
|
Roche And Genentech Sign Licensing Agreement For Herceptin
|
|
|
Genentech Reports 1998 2nd Quarter Results
|
|
|
U.S. Stroke Study Halted Due to Lack of Clinical Benefit Observed in Patients Treated After Three Hours
|
|
|
Pivotal Clinical Trial of First Monoclonal Antibody
|
|
|
FDA Advisory Committee Recommends Approval of First Monoclonal Antibody for Metastatic Breast Cancer
|
|
|
Genentech and South San Francisco Celebrate Six-Year Anniversary of Community Program
|
|
|
Genentech Reports Third Quarter Results
|
|
|
Genentech and Alkermes Announce Positive Preliminary Results of Phase III Clinical Trial of Nutropin Depot®
|
|
|
Genentech Dedicates $250 Million Vacaville Facility
|
|
|
Genentech Names Barta Vice President, Quality
|
|
|
New Investigational Data Show Monoclonal Antibody to IgE May Reduce Seasonal Allergy Symptoms
|
|
|
Rituxan Follow-Up Data Shows 28 Percent of Responders Still in Remission
|
|
|
Genentech Appoints Dilly Vice President of Medical Affairs
|
|
|
Genentech Named One of Fortune's 100 Best Companies to Work For in America
|
|
|
Pulmozyme Receives FDA Approval for Labeling Change
|
|
|
Biotechnology Breakthrough In Breast Cancer Wins FDA Approval
|
|
|
Genentech Reports 1995 Second Quarter Results
|
|
|
Genentech and Scios Nova Enter Into Agreement for Development of Acute Kidney Failure Treatment
|
|
|
Genentech and Lilly Reach Settlement
|
|
|
Genentech Reports 1994 Fourth Quarter Results
|
|
|
ITC Votes Not to Review Judge's Decision
|
|
|
Accelerated Infusion Regimen of Activase Cleared by FDA for U.S. Marketing
|
|
|
Genentech Reports Strong 1995 First Quarter Results
|
|
|
Genentech and IDEC Pharmaceuticals to Collaborate on Anti-CD20 Monoclonal Antibody for B-Cell Lymphomas
|
|
|
Genentech and Roche Change Form of Transaction to Accommodate New Schedule for Stockholder Vote
|
|
|
Judge Grants Genentech's Request for Preliminary Injunction Prohibiting Sale of Novo Nordisk's Growth Hormone
|
|
|
Review Board Recommends Termination of Phase III Study of Pulmozyme in Chronic Obstructive Pulmonary Disease
|
|
|
Genentech Granted Preliminary Injunction Prohibiting Sale of Bio-Technology General (BTG) Human Growth Hormone Product
|
|
|
Genentech Receives Favorable Ruling on Process Patent Applicaiton for Recombinant Human Factor VIII:C
|
|
|
Genentech Completes Negotiations, Purchases Land For New Manufacturing Facility in Vacaville, CA
|
|
|
Ed Jennings Cleared of All Charges
|
|
|
Genentech Submits NDA for Nutropin in Turner's Syndrome
|
|
|
Genentech's Blood Platelet Factor (TPO) Enters the Clinic as Phase I Trial Begins
|
|
|
Genentech Stockholders Approve Roche's Extended Buyout Option
|
|
|
Brewer Resigns as Genentech's Senior VP of Sales & Marketing
|
|
|
Patent Claims Upheld for Genentech's t-PA in Europe
|
|
|
Genentech Reports 20 Percent Increase in Earnings for Third Quarter 1995
|
|
|
Cutter To Receive Factor VIII License From Genentech
|
|
|
Promising New Anti-Cancer Drug Produced By Genentech
|
|
|
Xanelim (Efalizumab) Study Results Presented at 60th Annual American Academy of Dermatology Meeting
|
|
|
Genentech to Collaborate with ABC2 for Brain Cancer Research
|
|
|
Phase III Tracleer (bosentan) Study in Chronic Heart Failure Does Not Meet Primary Efficacy Objective
|
|
|
Genentech Names Mark Ahn Vice President, Hematology Sales and Marketing
|
|
|
New England Journal of Medicine Study Shows 53 Percent Increase in Event-Free Survival in Patients Treated with Rituxan and CHOP Chemotherapy
|
|
|
Genentech Named One of Fortune's "100 Best Companies To Work For"
|
|
|
Genentech Exceeds $2 Billion in Revenues with $1 Billion in Oncology Sales
|
|
|
Genentech Announces January 16 Webcast Discussion of Earnings and Other Business Results
|
|
|
Genentech Granted Fundamental U.S. Patent for Antibody Technology
|
|
|
Genentech Receives FDA Approval to Add Survival Data to Herceptin Product Labeling
|
|
|
Clinical Trial Data Presented on Rituxan with Chemotherapy as Front-Line Treatment in Chronic Lymphocytic Leukemia (CLL)
|
|
|
Potential Extended Survival Benefit Shown with Rituxan and Chop Chemotherapy Study as Front-Line Therapy in Common Forms of Non-Hodgkin's Lymphoma (NHL)
|
|
|
Investigational Data Presented on Use of Rituxan in the Treatment of Immune Thrombocytopenic Purpura (ITP)
|
|
|
Key Milestones Achieved in Genentech's Biooncology Initiative
|
|
|
FDA Advisory Committee Unanimously Recommends Approval of Breast Cancer Test to Select Candidates for Herceptin Therapy
|
|
|
Genentech Invites Public to Listen to Webcast of December 10 Discussion of Rituxan Presentations at the American Society of Hematology Meeting
|
|
|
Genentech Announces Stock Repurchase Program
|
|
|
Genentech Announces Four Senior Appointments in Development and Product Operations
|
|
|
Genentech and Novartis Update Xolair BLA Amendment Timeline
|
|
|
National Cancer Institute (NCI) Trial Studying Genentech's Avastin in Advanced Kidney Cancer Reaches Pre-Specified Efficacy Endpoint Early
|
|
|
No Verdict Reached in Genentech, City of Hope Contract Dispute
|
|
|
Genentech Reports 34 Percent Increase in Product Sales for Third Quarter
|
|
|
Genentech Named Among 100 Best Companies for Working Mothers
|
|
|
Genentech and Xoma Update Xanelim BLA Filing Timing
|
|
|
Genentech Announces October 10 Webcast Discussion of Earnings and Other Business Results
|
|
|
FDA Approves Cathflo Activase® (Alteplase) To Restore Function To Central Venous Access Devices As Assessed By The Ability To Withdraw Blood
|
|
|
ASSENT 3 Trial Shows Heart Attack Patients May Benefit From New Treatment Regimen: Clot-Buster Plus Low-Molecular-Weight Heparin
|
|
|
Genentech Appoints Andrew C. Chan to Senior Director of Immunology
|
|
|
Xanelim Shows Initial Positive Results in Second Pivotal Phase III Study
|
|
|
Genentech Invites Public to Listen to Webcast of July 31 Discussion of Xanelim Phase III Results
|
|
|
Genentech Foundation for Biomedical Sciences Awards $766,000 to Local Community Programs
|
|
|
Genentech Reports 33 Percent Increase in Product Sales for Second Quarter
|
|
|
FDA Issues Complete Response Letter for Xolair (Omalizumab)
|
|
|
Genentech Announces July 11 Webcast Discussion of Earnings and Other Business Results
|
|
|
Xanelim in Pivotal Phase III Study Shows Initial Positive Results
|
|
|
Genentech Invites Public to Listen to Webcast of June 21 Discussion of Xanelim Phase III Results
|
|
|
Schwarz Pharma's Rights to Growth Hormone Products Reacquired by Genentech
|
|
|
Genentech Names Thomas T. Thomas Treasurer
|
|
|
Phase III Clinical Trials of Xanelim Humanized Monoclonal Antibody for Moderate-to-Severe Psoriasis Show Preliminary Positive Results
|
|
|
Genentech Appoints David Ebersman Senior Vice President, Product Operations
|
|
|
Positive Investigational Data Presented On Rituxan Plus Fludarabine As Potential Front-Line Therapy For Chronic Lymphocytic Leukemia
|
|
|
OSI Pharmaceuticals, Genentech and Roche Announce Clinical Data From Phase II Ovarian Cancer Trial of Tarceva (OSI-774)
|
|
|
FDA Approves Expanded Use of Rituxan for Treatment of Low-Grade Non-Hodgkin's Lymphoma (NHL)
|
|
|
Addition of Herceptin to Chemotherapy Demonstrates 50 Percent increase in Survival Benefit in Patients Selected by FISH
|
|
|
OSI Pharmaceuticals, Genentech and Roche Announce Interim Clinical Data From Phase II Cancer Studies of the Anti-EGFR Therapy Tarceva® (OSI-774)
|
|
|
Genentech Wins Patent Dispute With GlaxoSmithKline
|
|
|
Genentech Invites Public to View Webcast of May 10 Annual Meeting of Stockholders
|
|
|
Oral Endothelin Receptor Antagonist Tracleer Meets Primary Endpoint In Pulmonary Arterial Hypertension Study
|
|
|
Phase III Clinical Trial of Veletri for the Treatment of Acute Heart Failure Symptoms Does Not Meet Primary Efficacy Objective
|
|
|
Genentech Reports 38 Percent Increase in Product Sales for First Quarter
|
|
|
Genentech Appoints Kimberly Popovits Senior Vice President, Marketing and Sales, for CardioPulmonary and Specialty Markets
|
|
|
Genentech and Biotech Celebrate 25 Years of Scientific and Medical Innovation
|
|
|
Genentech Announces April 12 Webcast Discussion of Earnings and Other Business Results
|
|
|
First Endothelin Receptor Antagonist Shows Positive Preliminary Results for Acute Heart Failure
|
|
|
Genentech and Actelion Announce March 20 Webcast Discussion of Veletri (Tezosentan) RITZ-2 Trial Results
|
|
|
Study Published in New England Journal of Medicine Demonstrates Herceptin with Chemotherapy Increases Median Survival in Women with Metastatic Breast Cancer
|
|
|
Genentech And Novartis Update Expectations For FDA Review Of Xolair Biologics License Application
|
|
|
Genentech Names Robert Garnick Senior Vice President, Regulatory, Quality And Compliance
|
|
|
Genentech Invites Public to Listen to February 21, 2001 Webcast
|
|
|
Phase III Trial of Intravenous Endothelin Receptor Antagonist Tezosentan for Acute Heart Failure Shows Positive Hemodynamic Results
|
|
|
Genentech Reports 30 Percent Increase in Net Income and 28 Percent Increase in Earnings Per Share for 2000
|
|
|
Genentech Names John Whiting Vice President
|
|
|
Genentech Announces January 18 Webcast Discussion of Earnings and Other Business Results
|
|
|
Genentech and Alkermes to Expand Clinical Development of Nutropin Depot
|
|
|
COR, Schering-Plough, and Genentech Announce U.S. Collaboration for INTEGRILIN® (eptifibatide) Injection, TNKaseTM (Tenecteplase) and Activase® (Alteplase, Recombinant)
|
|
|
OSI Pharmaceuticals, Genentech and Roche Team up to Deveolp and Commercialize OSI-774, OSI's Leading Cancer Drug to Develop and Commercialize OSI-774, OSI's Lead Cancer Drug
|
|
|
Names Richard H. Scheller Senior Vice President, Research
|
|
|
Genentech Names Claudia Estrin Vice President, Decision Support and Commercial Innovation
|
|
|
Genentech Named One Of Fortune's "100 Best Companies To Work For In America"
|
|
|
Actelion and Genentech Sign Licensing Agreement for Tracleer (Bosentan) in the U.S.
|
|
|
Phase III Trials Underway Evaluating Herceptin In Early Stage Breast Cancer
|
|
|
New Investigational Data Presented on Rituxan Plus Chemotherapy as Potential Front-Line Therapy
|
|
|
Potential Survival Benefit Shown with Rituximab and CHOP Chemotherapy in Aggressive Non-Hodgkin's Lymphoma
|
|
|
Genentech Reports 25 Percent Increase in Product Sales for Third Quarter
|
|
|
Genentech Announces 2-For-1 Stock Split Effective October 17
|
|
|
Genentech Announces Filing of Supplemental Biologic License Application
|
|
|
Genentech Appoints Nagler to Vice President of Human Resources
|
|
|
Genentech Launches Annual Community Relations Program to Boost Local Economic Development
|
|
|
Genentech Appoints Joseph S. McCracken Vice President, Business Development
|
|
|
Genentech Reports 15 Percent Increase in Product Sales for Second Quarter
|
|
|
Genentech CEO Says Amgen/TKT Trial Outcome Not a Bellwether for Biotech
|
|
|
Genentech Announces Phase II Trial of Experimental Anti-CD18 Antibody Did Not Meet Its Primary Objectives
|
|
|
Genentech and Novartis Submit Application for FDA Approval of Anti-IgE Antibody
|
|
|
FDA Approves New, Single-Injection Clot Buster TNKase (Tenecteplase) For Treatment Of Heart Attack
|
|
|
Genentech Appoints Andrew Scherer Vice President, Engineering and Facilities
|
|
|
Preliminary Positive Phase II Results for Experimental Anti-VEGF Monoclonal Antibody with Chemotherapy in Lung Cancer Presented at ASCO
|
|
|
Single Agent Herceptin Demonstrates 26 Percent Response Rate as Front-Line Metastatic Breast Cancer Therapy in Phase II Trial
|
|
|
Anti-VEGF Monoclonal Antibody with Chemotherapy Demonstrates Preliminary Positive Phase II Results in Colorectal Cancer
|
|
|
Genentech Names Roy C. Hardiman Vice President, Corporate Law
|
|
|
Genentech Appoints Myrtle Potter to EVP of Commercial Operations and COO
|
|
|
ImmunoGen and Genentech Form Multi-Product Collaboration to Develop Tumor-Activated Prodrugs
|
|
|
ImmunoGen and Genentech Sign Exclusive License Agreement
|
|
|
Immunex and Genentech Moving Forward with Preclinical Development Program of TRAIL/Apo2L
|
|
|
Genentech's Vacaville Facility Granted FDA Licensure
|
|
|
Genentech Reports 21 Percent Increase in Product Sales for First Quarter
|
|
|
Genentech Purchases Cell Culture Manufacturing Facility in Spain
|
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Genentech Appoints Kraines Vice President of Finance
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Offering by Roche of 17.3 Million Genentech Shares Priced at $163 Per Share
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Roche to Launch Offering of Up to 19 Million Genentech Shares
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Genentech Announces Clinical Trials Testing TNKase (Tenecteplase) with Leading Anti-Thrombotics for Treatment of Heart Attack
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Genentech Issues Important Drug Notification for Pulmozyme Due to Packing Defect
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Studies Show Investigational Compound May Help Improve Control of Asthma Exacerbations While Reducing the Need for Steroids and Rescue Medication
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Actelion and Genentech Sign Licensing Agreement for Tezosentan in the U.S.
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Genentech Reports 1999 Year-End Results
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Genentech to File Motion and Appeal to Maintain Injunction Against BTG
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Roche to Issue Exchangeable Bonds
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Judge Finds Growth Hormone Patent Infringement by Novo-Nordisk and BTG; Recommends Dismissal of Complaint On Technicality
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Study Reaffirms Benefits of Activase t-PA
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Genentech Locates Major New Facility in Vacaville, CA
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Genentech Reports 1994 Third Quarter Results
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Genentech Names Louis J. Lavigne, Jr. Senior Vice President and Stephen Juelsgaard Vice President and General Counsel
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Genentech Names Dennis Henner and Bryan Lawlis Vice Presidents
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Genentech Opposes Recommendations to Make Growth Hormone a Scheduled Drug
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Genentech Employee Indicted on Charges of Violating Medicare/Medicaid Anti-Remuneration Laws as a Result of Federal Investigation in Minnesota
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Genentech Reports 1994 Second Quarter Results
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Genentech Responds to Ruling Regarding t-PA Patent Infringement by Genetics Institute
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Local Elementary School Students 'Go To Town' with Genentech Employees in South San Francisco
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Genentech Reports Discovery of New Blood Platelet Factor
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FDA's Cardio-Renal Advisory Committee Unanimously Recommends Accelerated Activase t-PA Label Change by FDA
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Genentech Names Polly Moore and Robert Garnick to Vice Presidents
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Genentech Extends Benefits Coverage to Same-Sex Domestic Partners
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Genentech Files Suit Against Centocor
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Genentech Reports 1994 First Quarter Results
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Pulmozyme Introduced in Ireland
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Pulmozyme Phase II Clinical Study Completed in Hospitalized Chronic Bronchitis Patients
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Genentech to Provide Growth Hormone Products Through PCS Pharmacy Network
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FDA Grants Genentech License to Market Nutropin for Growth Hormone Deficiency in Children
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Genentech Receives U.S. Patent for Transforming Growth Factor Beta (TGF)
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Genentech Begins Construction of $58 Million Laboratory Facility in South San Francisco
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Genentech Files Suit against Tanox Biosystems
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Genentech Reports 1993 Fourth Quarter And Year End Results
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Settlement Reached in Factor VIII Litigation Involving Genentech, Miles, The Scripps Research Institute and Rhone-Poulenc Rorer
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Pulmozyme Becomes Available to Cystic Fibrosis Patients
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FDA Grants Genentech License to Market Pulmozyme
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J. Beers Named General Manager of Genentech Canada, Inc.
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Genentech Receives FDA Approval to Market Nutropin for Growth Failure Due to Chronic Renal Insufficiency
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FDA Advisory Committee Unanimously Recommends Approval for Nutropin as Treatment for Growth Failure in Children with Chronic Renal Insufficiency
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Genentech Unveils $10 Million Program for High School Biology Teachers
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Genentech Reports Third Quarter Results
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Study Shows Alteplase t-PA Significantly Reduces Death Up To 12 Hours After Heart Attack Begins
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Activase Regains Marketshare
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STILE Study for Peripheral Arterial Occlusion Discontinued
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FDA Advisory Committee Unanimously Recommends Pulmozyme (DNase) for Approval as Cystic Fibrosis Treatment
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Genentech Granted Permanent Injunction in Wellcome Litigation Over t-PA Patents
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Genentech Reports Second Quarter Results
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Genentech Issued Pioneering Basic Processes Patent; Files Suit Against Lilly for Infringement
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Bio Holds First Board Meeting, Genentech CEO Elected Chairman
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41,000 Patient Gusto Trial Shows Activase t-PA Most Effective Clot-Buster to Save Lives of Heart Attack Patients
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Genentech Reports First Quarter Results
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Genentech Joins Coalition in Favor of Biodiversity Treaty
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Genentech Files Regulatory Applications to Market Pulmozyme (dornase alfa) DNase for Cystic Fibrosis in the United States, Canada, Europe
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Press Statement: Government-Imposed Price Controls Would Strangle Investment and Raise Health Care Costs
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Genentech Files Complaint with International Trade Commission to Enforce Growth Hormone Patents
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Genentech Announces Collaboration with GenVec to Develop Gene Therapy for Cystic Fibrosis
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Genentech French Patent Partially Revoked
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Genentech Reports Fourth Quarter and Year End Results
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Genentech Names Kurt Kopp to Head European Organization
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Genentech Receives U.S. Patent for Recombinant Human Nerve Growth Factor
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Pulmozyne(TM)(rhDNase) III Clinical Study Completed in Cystic Fibrosis
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Genentech Opens World's Largest Biotechnology Research Facility
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Genentech Reports Third Quarter Results
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Genentech Elects Linda Fayne Levinson To Board Of Directors
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Study Shows Altepase t-PA Significantly Reduces Mortality Up to 12 Hours After Heart Attack Begins
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Court Rules in Favor of Genentech in t-PA Patent Dispute
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Genentech Reports Second Quarter Results
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Xenova Receives Additional Equity Investment from Genentech, Inc.
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Genentech Secures European Patent for t-PA
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Genentech Reports First Quarter Results
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Genentech Names Gregory Baird Vice President of Corporate Communications
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Genentech Enters International Commercial Development and Marketing Agreement with Roche for DNase
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Genentech Reports Fourth Quarter and Year End Results
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Tularik Inc. Formed to Pursue Novel Biopharmaceutical Approach
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Wellcome and Sandoz Out-License Genentech Monoclonal Antibidody Patent
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Genentech Announces Auction of Vitamin C Concern
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Genentech Wins First Major Japanese Biotechnology Patent Case
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Genentech Announces Third Quarter Earnings
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Genentech and Xenova Announce New $20 Million Agreement
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Incyte And Genentech To Develop Drug For Treating Septic Shock
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Genentech Promotes Marty Glick to Vice President and Treasurer
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Genentech Reports Second Quarter Results
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Roche and Genentech Reach Agreement Over Human Growth Hormone Patent Dispute
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Genentech's t-PA Launched in Japan
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Genentech Announces First Quarter Results
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Genentech to Test Potential Therapy for Breast and Ovarian Cancers
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New gp120 AIDS Vaccine Enters NIAID Clinical Trials
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ISIS-3 Results Controversial and Inconclusive for U.S. Practice; T-PA Used in ISIS-3 Study Not Genentech's Product
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Judge Requires Beecham To Abide By Court Promises Concerning ISIS-3 Ads
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SmithKline to Stop Misleading ISIS-3 Ads
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Genentech Seeks Federal Court Order to Stop Beecham's False Advertising of Heart Attack Drugs
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FDA Grants Genentech Orphan Drug Status for DNase, a Potential Cystic Fibrosis Treatment
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Telios Pharmaceuticals and Genentech to Develop Anti-Clotting Drug
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Xenova and Genentech Expand Their Research and Development Collaboration
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Genentech Reports Fourth Quarter Earnings
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Genentech and Glycomed Announce Pact to Develop Carbohydrate-Based Therapeutics
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HHS News U.S. Department of Health and Human Services
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Genentech Granted Product License for Interferon Gamma-1B
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Genentech to Broadly License Key Monoclonal Antibody Patent
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Genentech Reaches an Agreement to Settle Class Action Litigation
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Study Begins to Test gp120 as a Potential Immune System Booster in HIV Infection
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Genentech Announces Third Quarter Results
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Genentech to Build $75 Million Research Center
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European Co-operative Study Group for Recombinant Tissue-Type Plasminogen Activator (rt-PA)
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Genentech and Roche Merger Transaction Completed
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Roche and Genentech to Complete Merger Transaction On or About September 7
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Genentech and Abott Settle Litigation Over t-PA Patents
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Genentech Promotes Arthur D. Levinson to Vice President of Research
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Genentech Promotes Marty Glick to Treasurer
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Genentech and Roche Certify Substantial Compliance with FTC Request
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Genentech Reports Second Quarter Results
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Genentech Stockholders Approve Roche Agreement
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Motion to Enjoin Vote at Genentech Stockholder Meeting Denied
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FDA Approves t-PA for Pulmonary Embolism
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Genentech Research on Protection of Chimpanzees from HIV Infection to be Published
|
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Genentech Announces Potential Therapy for Cystic Fibrosis
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Genentech Receives Important Process Patent For Gamma Interferon
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Genentech Issues Proxy on Roche Merger; Annual Meeting Set for June 8
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Genentech Reports First Quarter Results
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Genentech Wins Key t-PA Patent Cases in U.S. Federal Court
|
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Roche-Genentech Transaction Passes Exon-Florio Review
|
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Federal Trade Commission Requests More Information on Genentech-Roche Merger
|
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New Trial Results Inconclusive for U.S. Practice; Role of Heparin in Gissi-2 Questioned
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Genentech Begins Clinical Trials of Relaxin
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Genentech and Roche Holding LTD Form Pioneering Relationship; Roche to Own 60 Percent of an Independent Genentech
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Physicians Choose Activase as Preferred Heart Attack Treatment for Themselves
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Revised Development Plans Announced for CD4-based Products, Potential AIDS Therapeutics
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Biogen and Genentech Enter Into Cross-License Agreement for Gamma Interferon in The United States
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Genentech Fourth Quarter Revenues Up 24 Percent; 1989 Revenues Top $400 Million
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Genentech Surpasses 1989 Product Sales Goals
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Genentech Acquires Full Ownership of Canadian Operation
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Genentech Files FDA Application to Market Gamma Interferon in The United States
|
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TGF-beta Patent Issued December 12, 1989
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Genentech Sponsors Programs for Pharmacists "Building A New Pharmacopeia" Premieres at ASHP
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Genentech Appoints Gary Lyons Vice President -- Business Development
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Genentech Appoints Richard Brewer Vice President- Marketing
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Competitors Merge Marketing Strength to Co-Promote t-PA, Blood-Clot-Dissolving Agent, in Germany
|
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Genentech Third Quarter Profits Higher
|
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Genentech Receives Third Patent for Gamma Interferon
|
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Genentech Begins Clinical Trials of Insulin-Like Growth Factor
|
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Genentech Awards First Scientific Fellowship to David Goeddel
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Genentech Appoints M. David MacFarlane Vice President -- Regulatory Affairs
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Genentech rCD4 Partnership Raises $72.5 Million
|
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Genentech Promotes Murphy and Adds Rogers to Public Relations Staff
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Genentech Receives Additional United States Patent for t-PA
|
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Genentech Reports Second Quarter Earnings
|
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Genentech Expands CD4 Clinical Trials for AIDS
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Genentech Appoints David Beier Vice President - Government Affairs
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Genentech Opens Corporate Day Care Center
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Genentech Reports First Quarter Earnings and Increase in Activase Sales
|
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Genentech Scientists Share 1989 Investor of the Year Award
|
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Cross-Licensing Agreement Reached on Factor VIII Genetically Engineered Clotting Agent for Hemopheliacs
|
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FDA Approves Reduced Mortality Claim for Heart Attack Drug
|
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|
Genentech Anounces Activase Co-Promotion Agreement
|
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Genentech Will Not Appeal British t-PA Patent Case
|
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|
Genentech Reports 1988 Financial Results
|
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|
Genentech Meets Sales Forecast and Announces Two Collaborative Agreements
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|
Genentech, Cal Bio Announce Neonatology Product Agreement
|
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|
Licensing of Activase Marks New Era in Treating Heart Attacks
|
|
|
T-PA Approved in Canada
|
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|
Genentech's Patent on Basic Recombinant DNA Technology Issues in The United States
|
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Genentech Reports Third Quarter Results
|
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Genentech Appoints Two Vice Presidents
|
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T-PA Approved in West Germany
|
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|
T-PA Approved in South Korea
|
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Genentech Files Patent Suit on t-PA
|
|
|
T-PA Approved in Austria
|
|
|
Genentech Reports Second Quarter Results
|
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|
Britain's High Court Rules on t-PA Patent Dispute
|
|
|
Mitsubishi Chemical Industries and Genentech Agree to Commercialize Research Products
|
|
|
T-PA Approved in France
|
|
|
FDA Committee Reviews Activase t-PA
|
|
|
Genentech Reports First Quarter Results
|
|
|
FDA Cardiorenal Advisory Committee to Review t-PA
|
|
|
Genentech Completes Sale of $150 Million Convertable Subordonated Debentures in Europe
|
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|
Genentech Files Lawsuit Against FDA for Legalization of Orphan Drug Standards for Human Growth Hormone
|
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|
Genentech Reports Substantial Increase in 1986 Financial Results
|
|
|
Progress on Genentech t-PA Patent Application in Japan
|
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|
Genentech Completes Early Buyout Or First Two R&D Partnerships
|
|
|
Genentech Partnership Purchases Recieve Majority Approval
|
|
|
Genentech Names Chief Financial Officer
|
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|
Genentech Proposes Early Partnership Buyout
|
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|
Genentech Reports Third Quarter Results
|
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|
Genentech To Defend Patent Suit
|
|
|
Genentech Names Four Vice Presidents
|
|
|
Genentech Elects New Director to Its Board
|
|
|
Genentech Reports Second Quarter Results
|
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|
Genentech Reports First Quarter Results
|
|
|
Genentech's T-PA Patent Issues in the United Kingdom Today Suit Against Wellcome Follow
|
|
|
Genentech Reports Substantial Increase in 1985 Revenues and Income
|
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|
Genentech Announces 2 For 1 Stock Split
|
|
|
Genentech Awarded Orphan Drug Status For Growth Hormone
|
|
|
Business Venture Formed for Vitamin C Process Development
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|
Genentech Reports Third Quarter Results
|
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|
FDA Approves Genentech's Drug to Treat Children's Growth Disorder
|
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|
Genentech Reports Second Quarter Results
|
|
|
Recombinant DNA Technology
|
|
|
Genentech and Major European Pharmaceutical Firm Announce Institute for Cancer Research
|
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|
Genentech Reports First Quarter Results
|
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|
Genentechs Answer to Pituitary Derived Growth Hormone: Recombinant DNA Technology
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|
Susan Atkins Joins Genentech
|
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|
Genentech Forms Canadian Marketing Joint Venture With Major Pharmaceutical Company
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|
Genentech Offers 1 Million Of Common Stock At $45 Per Share
|
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|
Genentech Plans To File For Public Offering
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|
Genentech Reports Substantial Increase in 1984 Revenues and Income
|
|
|
Media Advisory
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Genentech Clinical Partners III Raises $30.7 Million For The Development Of TNF
|
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|
Genentech Reports Third Quarter Results
|
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|
Genentech Reports on Meeting with FDA Advisory Committee
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|
Genentech, Inc. Reports Second Quarter Results
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|
Genentech Expands Its Patent Department
|
|
|
Genentech Reports First Quarter Results
|
|
|
King of Sweden Presents Genentech President with Membership in Royal Swedish Academy
|
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|
Genentech Has Begun Human Evaluation of t-PA in Heart Attack Victims
|
|
|
Genentech Reports Significant Increase in 1983 Revenues and Income
|
|
|
Genentech President Gives Stock Analysts Preview Of 1983 Results and Beyond
|
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|
Travenol And Genentech Sign Definitive Agreement To Form Diagnostics Joint Venture
|
|
|
Genentech Begins Human Evaluation of Human Gamma Interferon
|
|
|
Genentech and Major European Pharmaceutical Firm Announce Commercialization Agreement on T-PA
|
|
|
Travenol and Genentech to Form Diagnostics Joint Venture
|
|
|
Dr. Goeddel Of Genentech Receives Prestigious Eli Lilly Award
|
|
|
Media Advisory
|
|
|
Genentech Reports Third Quarter Results
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|
|
Genentech, Inc. and Granada Announce bovine interferon R&D Agreement
|
|
|
Genentech Reports Second Quarter Results
|
|
|
Hewlett-Packard and Genentech Form Joint Venture
|
|
|
Genentech Clinical Partners II Raises $34 Million for The Development of t-PA
|
|
|
Possible Collaboration Between Genentech And Hewlett-Packard
|
|
|
Genentech Obtains Exclusive Development Rights on T-PA
|
|
|
Genentech Appoints Four Vice Presidents
|
|
|
Genetech Plans to Form New R&D Partnership for TPA Development
|
|
|
Genentech 1982 Revenues and Net Income Up; Company Announces 3 For 2 Stock Split
|
|
|
Genentech Reports Third Quarter Results
|
|
|
First Recombinant DNA Product Approved By The Food And Drug Administration
|
|
|
Genentech Elects Two New Directors to Its Board
|
|
|
Genentech Plans to Meet Year-End Goals Despite a Third Quarter Loss
|
|
|
Genentech Establishes New Research Partnership
|
|
|
Geneticist Martin To Join Genentech as Vice President of Research
|
|
|
Genentech Announces New Vice-President
|
|
|
Genentech Announces Possible Research And Development Partnership
|
|
|
Genentech Reports Second Quarter Results
|
|
|
(TPA) Produced By Recombinant DNA Techniques
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|
|
Genentech, Inc. Contracts With Two Japanese Companies to Develop New Thrombolytic Agent
|
|
|
Mitsubishi Chemical Industries, Ltd. And Genentech, Inc. To Develop Human Albumin For Commercial Production
|
|
|
Genentech, Inc. Reports Results For First Quarter, 1982
|
|
|
Corning Glass, Genentech to Form Industrial Enzyme Company
|
|
|
Genentech Scientists Develop Bovine Interferon
|
|
|
Genentech Revenues Up 137% Net Income Up Slightly
|
|
|
Genentech Acquires Site For Future Facilities Expansion in South San Francisco
|
|
|
Human Serum Albumin Produced By Recombinant DNA
|
|
|
Genentech, Inc. Reports Third Quarterly Results
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|
|
Five Genentech Products Receive NIH Approval for Large Scale Production
|
|
|
The first successful expression of immune interferon by recombinant DNA
|
|
|
Swedish Group Invests $20 Million in Genentech
|
|
|
David Packard Elected to Board of Directors of Genentech
|
|
|
Genentech is Beginning Efficacy Studies with Human Growth Hormone in Children with Hypopituitarism
|
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|
First Major Investment by Japanese Interests in Genentech
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|
Genentech, Inc. Reports Second Quarter Results
|
|
|
Genentech, Inc., Reports First Quarter Revenues of $3.9 Million in 1981 vs. $1.6 Million in 1980
|
|
|
Genentech Reports Annual Revenues of $9.0 Million in 1980 Vs. $3.4 Million in 1979
|
|
|
FDA-Approved Clinical Tests on Humans Begin Today With Human Growth Hormone Made by Recombinant DNA
|
|
|
Flour Purchases Shares in Genentech
|
|
|
Genentech Files Registration Statement With SEC For Its Initial Public Offering
|
|
|
Genentech Announces Successful Production and Preliminary Biological Tests For Fibroblast and Leukocyte Interferon
|
|
|
Supreme Court Decision Will Spur Genetics Industry
|
|
|
First Successful Bacterial Production of Human Growth Hormone Announced
|
|
|
First Successful Laboratory Production of Human Insulin Announced
|
|
|
Genentech Forecasts 1988 Results
|
|
|
Ralph Snyderman, Genentech VP Named Chancellor at Duke University Medical School
|
|
|
New Drug Application For t-PA Filed in Japan
|
|
|
British Court of Appeals Rules in t-PA Patent Case
|
|
|
Genentech Reports Results For Third Quarter
|
|
|
Genentech Reports Shareholder Suits Filed
|
|
|
Genentech Sees Quarterly Earnings Flat With Last Year
|
|
|
Genentech Receives Second t-PA Patent in the United States
|
|
|
Genentech Wins Growth Hormone Patent Suit
|
|
|
Genentech Reports Increased Earnings, Sales in Second Quarter
|
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|
Axel Ullrich, Genentech Staff Scientist, Named Director of Max Planck Institute
|
|
|
Free Heart Drug To Needy, Uninsured Patients
|
|
|
Genentech Receives Broad t-PA Patent in the United States
|
|
|
Genentech Appoints Two Vice Presidents
|
|
|
Genentech Adopts Preferred Share Rights Purchase Plan
|
|
|
Genentech Reports First Quarter Earnings
|
|
|
Genentech Creates Foundation to Fund Basic Biotechnology Research
|
|
|
Genentech Announces New VP of Sales
|
|
|
Genentech Stock to be Listed on NYSE March 2
|
|
|
Genentech Names Three Vice Presidents
|
|
|
Genentech Elects New Director to Its Board
|
|
|
Genentech Reports Significant Increase in 1987 Financial Results
|
|
|
Genentech Announces Product Sales and NYSE Listing
|