Clinical Leadership

We have built a large, expert team to design and manage our clinical trials, the vital and lengthy phase following discovery and preclinical development.

Our Clinical Development and Regulatory Affairs group has more than 400 team members, including many with doctoral degrees and years of pharmaceutical-industry experience.

Peter Powchik, M.D. Peter Powchik, M.D.
Senior Vice President, Clinical Development

Ned Braunstein Ned Braunstein, M.D. 
Senior Vice President, Regulatory Affairs

Ingrid Adamsons, M.D., M.P.H. Ingrid Adamsons, M.D., M.P.H.
VP Pharmacovigilance and Risk Management

Graeme Currie Graeme Currie, Ph.D.
VP Clinical Project Management and Operations

Israel Lowy Israel Lowy, M.D., Ph.D.
VP Clinical Sciences Translational Science and of Oncology

Daniel Matarazzo Daniel Matarazzo, M.B.A.
Senior Director Clinical Finance

Scott Mellis Scott Mellis, M.D., Ph.D.
VP Clinical Sciences Translational Medicine

Robert Pordy Robert Pordy, M.D., FACP
VP Regulatory Development and Medical Safety

Yuhwen Soo Yuhwen Soo, Ph.D.
VP Biostatistics and Data Management

Beate Stych Beate Stych, M.D.
VP Medical Affairs

Robert Vitti Robert Vitti, M.D., M.B.A.
VP Clinical Sciences Ophthalmology

Steven Weinstein Steven Weinstein, M.D., Ph.D.
VP Clinical Sciences Immunology and Inflammation

This section discusses pipeline drug candidates currently undergoing clinical testing in a variety of diseases. The safety and efficacy of these drug candidates have not been evaluated by any regulatory authorities for the indications described in this section.

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