Craig Berman
Hoofd Techniek/Wetenschap/O&O bij SUTRO BIOPHARMA, INC.
Profiel
Craig Berman is currently the Vice President of Clinical Development at Sutro Biopharma, Inc. and QED Therapeutics, Inc. He received his undergraduate degree from Northwestern University in 1987 and his doctorate degree from the University of Colorado Health Sciences Center in 1992.
Actieve functies van Craig Berman
Bedrijven | Functie | Begin |
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SUTRO BIOPHARMA, INC. | Hoofd Techniek/Wetenschap/O&O | 21-05-2020 |
QED Therapeutics, Inc.
QED Therapeutics, Inc. Pharmaceuticals: MajorHealth Technology Part of BridgeBio Pharma, Inc., QED Therapeutics, Inc. is a biotechnology company based in Palo Alto, CA. The company focuses on precision medicine for FGFR-driven diseases and is committed to finding solutions to FGFR-driven cancers and diseases to give patients more possibilities. QED Therapeutics' lead investigational candidate is infigratinib, an orally administered, FGFR1-3 selective tyrosine kinase inhibitor that has shown activity in patients with chemotherapy-refractory cholangiocarcinoma with FGFR2 fusions and advanced urothelial carcinoma with FGFR3 genomic alterations. In 2020, QED submitted a new drug application (NDA) with the Food and Drug Administration for second- and later-line cholangiocarcinoma. Michael Henderson has been the CEO of the company since 2017. | Hoofd Techniek/Wetenschap/O&O | 01-10-2018 |
Opleiding van Craig Berman
University of Colorado Health Sciences Center | Doctorate Degree |
Northwestern University | Undergraduate Degree |
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Beursgenoteerde bedrijven | 1 |
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SUTRO BIOPHARMA, INC. | Health Technology |
Bedrijven in privébezit | 1 |
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QED Therapeutics, Inc.
QED Therapeutics, Inc. Pharmaceuticals: MajorHealth Technology Part of BridgeBio Pharma, Inc., QED Therapeutics, Inc. is a biotechnology company based in Palo Alto, CA. The company focuses on precision medicine for FGFR-driven diseases and is committed to finding solutions to FGFR-driven cancers and diseases to give patients more possibilities. QED Therapeutics' lead investigational candidate is infigratinib, an orally administered, FGFR1-3 selective tyrosine kinase inhibitor that has shown activity in patients with chemotherapy-refractory cholangiocarcinoma with FGFR2 fusions and advanced urothelial carcinoma with FGFR3 genomic alterations. In 2020, QED submitted a new drug application (NDA) with the Food and Drug Administration for second- and later-line cholangiocarcinoma. Michael Henderson has been the CEO of the company since 2017. | Health Technology |