Featured Researcher: Michael Pourdehnad – Bristol Myers Squibb

Michael Pourdehnad, MD

Michael Pourdehnad, MD

Senior Vice President, Early Clinical Development, Hematology/Oncology and Cell Therapy

Brisbane, CA


Michael Pourdehnad, MD, serves as the head of the Brisbane site and is senior vice president of Early Clinical Development, Hematology/Oncology and Cell Therapy. Michael leads early clinical development programs across both internal and partnered assets for a diverse range of treatment modalities, with a focus on targeted protein degradation. He and his team build on the early discovery work of colleagues in San Diego and Redwood City as assets are passed from the discovery phase to the clinic.


Michael leads a team focused on developing innovative cancer treatments to combat hard-to-treat diseases. He oversees early clinical development programs for a diverse range of treatment modalities such as cell therapy, protein degraders, T-cell engagers, monoclonal antibodies and small molecules. He and his team of physicians and clinical scientists use translational insights to shape clinical trials, guide biomarker strategies and inform asset development.  They work alongside discovery and translational teams to refine the therapeutic hypotheses around new drug targets. Then, as candidate drugs get closer to the clinic, they optimize biomarkers, determine patient selection strategies, select initial human dosing and combination strategies to enable faster and more effective drug development informed by core scientific principles and data. These insights shape clinical trials and inform asset development in solid tumors and hematologic malignancies.  


During his industry career, Michael has played a leading clinical role in the evolution of targeted protein degradation.  These potentially life-changing therapies harness the cell’s own machinery to degrade previously undruggable proteins required for cancer cell survival. Michael joined Bristol Myers Squibb by way of Celgene in 2019. At Celgene, he was part of the group that established the Protein Homeostasis Thematic Center of Excellence and has led all early clinical cereblon E3 ligase modulator (CELMoD) and ligand-directed degraders (LDD) programs since.  


Prior to joining Celgene, Michael was a member of the faculty in the hematologic malignancies and bone marrow transplant program at the University of California, San Francisco (UCSF). He continues to hold an active faculty appointment at UCSF, where he sees patients with hematology malignancies weekly. Michael earned his MD from the Chicago Medical School, received training in internal medicine at Mount Sinai Hospital in New York, and completed his hematology and oncology fellowship and post-doctoral laboratory training at UCSF. 

Interests and Expertise

Michael was touched by cancer when he lost a close friend to leukemia as a young adult. Early in his training as a physician-scientist, he found that the field combined his passion for caring for patients with his strong interest in working at the forefront of the molecular understanding of disease and targeted therapies.  


As a drug developer at Bristol Myers Squibb, Michael’s intellectual fulfillment comes from translating insights from the lab bench to the patient bedside and back to the lab again. Meanwhile, his weekly clinic caring for patients with hematologic malignancies keeps him grounded in the urgent needs of patients for new and better treatment options. Michael also values giving his time to training and mentoring the next generation of researchers and working closely with STEM initiatives in the community. 


Outside of work, Michael lives in San Francisco with his wife, two boys and their dog. They enjoy music/concerts, food, travel and being active in nature with friends.