Statements
Read our formal press statements on significant topics and events.
|
|
Update on Tamiflu SupplyGenentech has released a reserve stock of Tamiflu® (oseltamivir phosphate) 75 mg capsules that carry different packaging from what is currently available on the market in the U.S. |
Genentech statement on counterfeit drug labeled as Altuzan (bevacizumab) in the United States |
Statement on counterfeit drug labeled as Avastin® (bevacizumab) in the United States |
Statement on CAT trial data published in the New England Journal of Medicine |
Statement on Tamiflu® (oseltamivir phosphate) availabilityGenentech, a member of the Roche Group, announced today that ample supplies of Tamiflu (oseltamivir phosphate), a prescription antiviral medicine to treat flu, will be widely available at U.S. pharmacies this flu season. |
Statement on MAIN trialGenentech, Inc. announced today that it has accepted the recommendation of an independent Data and Safety Monitoring Board (DSMB) to stop enrollment into the MAIN trial, a Phase III clinical study evaluating the efficacy and safety of Avastin® (bevacizumab) when added to Rituxan® (rituximab) plus CHOP (cyclophosphamide/doxorubicin/vincristine/prednisone) chemotherapy in patients with Diffuse Large B-Cell Lymphoma (DLBCL). |
Statement on supplemental Biologics License Applications for Avastin® (bevacizumab)Genentech, Inc. announced today that the U.S. Food and Drug Administration's (FDA) Oncologic Drugs Advisory Committee (ODAC) will discuss the company's two supplemental Biologics License Applications (sBLAs) for Avastin® (bevacizumab) for the treatment of women who have not received chemotherapy for advanced (metastatic) HER2-negative breast cancer during an advisory committee meeting on July 20, 2010. |
Statement on study of Avastin® (bevacizumab)Genentech, Inc. announces study of Avastin® (bevacizumab) in early-stage breast cancer (E5103) will resume enrollment and continue as planned. |
Statement on FDA discussion of supplemental Biologics License ApplicationGenentech, Inc. announced today that the U.S. Food and Drug Administration's (FDA) Oncologic Drugs Advisory Committee (ODAC) will discuss the company's supplemental Biologics License Application (sBLA) for Avastin® (bevacizumab) for people with previously treated glioblastoma during an advisory committee meeting on March 31, 2009. |
Genentech statement on counterfeit drug labeled as Nutropin AQ® [somatropin (rDNA origin) injection] |
