Peter Dragovich
Principal Scientist, Discovery Chemistry
"I'm interested in identifying small molecules which can be utilized as novel therapeutic agents to treat serious diseases with unmet needs."
- 3
years at Genentech - 3
publications (2010-12) - 2
awards & honors
I began working as a chemist in the pharmaceutical industry in 1993 at Agouron Pharmaceuticals, a biotech company located in La Jolla (San Diego). During the next seven years at Agouron, I primarily worked on agents for the common cold (rhinovirus 3C protease inhibitors), first as intranasally delivered compounds and then as orally bioavailable agents. Two molecules from these efforts were advanced to human clinical trials. Over this time period, I also became increasingly interested in many other aspects of antiviral research. After the acquisition of Agouron by Warner-Lambert/Pfizer, I led the antiviral therapeutic area at Pfizer, La Jolla for the next five years. The teams working on the antiviral projects in La Jolla delivered eight development compounds during that time for the treatment of HIV, HCV, and respiratory diseases. Several of these compounds exhibited meaningful antiviral activity in patients and one is currently completing phase 2 studies in HCV.
In late 2005, I made the difficult decision to leave Pfizer and subsequently conducted both research and development work at Anadys Pharmaceuticals (another San Diego biotech). Over the next three years, the teams that I was part of identified an attractive non-nucleoside NS5B polymerase inhibitor and advanced it through a phase 1 POC study in HCV-infected patients. At that time, I left Anadys to pursue an opportunity to lead a newly-formed Chemistry Department at Roche Palo Alto which was focused on antiviral research. This chemistry group was unexpectedly moved to the Roche Nutley site less than one year after my arrival in Palo Alto. As a result of this change, I transferred to Genentech in early 2010 and have since been working in the immunology and oncology fields.
Featured Publication
Discovery of Tricyclic 5,6-dihydro-1H-pyridin-2-ones as Novel, Potent, and Orally Bioavailable Inhibitors of HCV NS5B Polymerase.
Bioorg. Med. Chem. Lett. 2009, 19, 6404.
Ruebsam F, Murphy DE, Tran CV, Li LS, Zhao J, Dragovich PS, McGuire HM, Xiang AX, Sun Z, Ayida BK, Blazel JK, Kim SH, Zhou Y, Han Q, Kissinger CR, Webber SE, Showalter RE, Shah AM, Tsan M, Patel RA, Thompson PA, Lebrun LA, Hou HJ, Kamran R, Sergeeva MV, Bartkowski DM, Nolan TG, Norris DA, Khandurina J, Brooks J, Okamoto E, Kirkovsky L.
View Abstract on PubMed
