About Us


CinRx is a biotechnology company founded in 2015 that leverages its team’s exceptional industry experience to develop therapeutics in a novel way that meets the modern paradigm of drug development. CinRx acquires compounds from multiple sources, as well as partners with other biotechnology companies, to invest in and develop innovative products that will transform the lives of patients. With its broad preclinical, clinical pharmacology, medical, biostatistical and regulatory expertise, CinRx accelerates drug development programs to help achieve marketing approval or bring about a successful commercial exit.


Jonathan Isaacsohn, MD, FACC

President and CEO, CinRx

August Troendle, MD

Chief Executive Officer, Medpace, Inc.

Jesse J. Geiger, CPA

President, Medpace, Inc.

Stephen P. Ewald, JD

General Counsel, Medpace, Inc.



Jon Isaacsohn
Founder and CEO
Dr. Jon Isaacsohn has more than 30 years of experience developing hundreds of drugs from protocol design to global submissions (including 30 NDAs) and was the co-founder of Medpace, Inc. He has decades of experience in academia, pharmaceuticals and clinical medicine. Dr. Isaacsohn formerly served as the Chief Medical Officer of Teva, where he was responsible for specialty drug development, including about 160 clinical trials, as well as the company’s New Therapeutic Entity Initiative, the safety of all marketed products and the Global Health Program.

Brian Murphy

Brian Murphy
Chief Medical Officer
Brian Murphy, MD, MPH is board-certified in infectious disease, internal medicine and pediatrics, and has more than 15 years of experience in clinical trial and drug development as an academic investigator and Vice President of Medical Affairs at Medpace. He has worked with large and small biopharmaceutical companies, government agencies, public-private partnership, and academic centers to achieve the approval of multiple products across various therapeutic areas.

Mary Bond-31366WEB

Mary Bond
Chief Translational Science Officer
Mary Bond, MS, MBA has more than 20 years of industry experience in early clinical development, leading numerous clinical pharmacology programs for both small and large molecules at SmithKline Beecham, GlaxoSmithKline, Cephalon, and Teva. She has been responsible for the design and oversight of more than 100 early phase studies and has contributed to more than 12 INDs/CTAs and 15 marketing applications both in the U.S. and abroad.



5375 Medpace Way
Cincinnati, OH 45227