Ranjit Bindra
Professor Yale Univerisity
Dr. Ranjit Bindra is a physician-scientist at the Yale School of Medicine, the Harvey and Kate Cushing Professor of Therapeutic Radiology, and the Scientific Director of the Yale Brain Tumor Center. Clinically, he treats adult and pediatric primary CNS cancers, as well as brain metastases using radiosurgery.
In the laboratory, his group recently led a team of four major laboratories at Yale, which reported the stunning discovery that IDH1/2-mutant tumors harbor a profound DNA repair defect that renders them exquisitely sensitive to PARP inhibitors. This work was published in Science Translational Medicine, Nature Genetics, and most recently in Nature, and it has received international attention with major clinical implications. Dr. Bindra is now translating this work directly into patients, in multiple phase I/II clinical trials. Most recently, Dr. Bindra discovered a novel approach to exploit DNA repair defects in cancer via DNA modification, which his group published in Science.
As an active biotech entrepreneur, he has founded six companies based on work from his laboratory, including Cybrexa Therapeutics, which is now in Phase I clinical trials. More recently, he founded Alphina Therapeutics, an early-stage biotech focused on targeting NAD metabolism in cancer, and Modifi Bio, based on DNA modification to exploit DDR defects. Under Bindra’s leadership as interim CEO, Modifi Bio was acquired by Merck and Company in the Fall of 2024.
Dr. Bindra received his undergraduate degree in Molecular Biophysics and Biochemistry from Yale University in 1998, and both his MD and PhD from the Yale School of Medicine in 2007. He completed his medical internship, radiation oncology residency, and post-doctoral research studies at the Memorial Sloan-Kettering Cancer Center (MSKCC) in 2012.
Seminars
- Tracing the journey of a groundbreaking technology, targeted DNA modification, from its initial discovery at the research bench to its successful translation into a biotech platform
- Detailing the strategic and financial evolution of the technology, highlighting how it attracted investment and ultimately led to a significant acquisition by a major pharmaceutical company
- Examining the path forward for this therapy, exploring how a promising scientific concept, now backed by a major pharma’s resources, is being advanced from the lab to clinical development and ultimately, to the patient’s bedside
- Identifying specific data packages, preclinical models and clinical milestones that will make a GBM asset attractive for a partnership, beyond scientific novelty
- Strategies for pitching, due diligence considerations and building collaborative relationships to effectively engage with big pharma business development teams to secure a deal
- Insights into creative deal terms, IP considerations and defining clear roles and responsibilities to ensure both partners are aligned on the path to clinical and commercial success