Rarebase, a platform drug development biotechnology company, has appointed Chris Moxham, President. In addition to continuing to serve as chief scientific officer, Moxham will be responsible for driving the company’s strategic plan for growth.

Moxham’s career spans more than 25 years in drug discovery focused on cutting-edge science and drug hunting in large pharma and biotech. He spent two decades at Eli Lilly and Co. where he helped bring over 10 molecules into the clinic across multiple therapeutic areas and across both small and large molecules.

Most recently Chris was CSO at Fulcrum Therapeutics, a clinical stage biotech focused on rare diseases, where he was responsible for the full range of drug discovery, translational science and early development activities including building and advancing the company’s preclinical portfolio through Phase 1 clinical trials. He was the scientific lead for FTX-6058 that is currently in phase 1 clinical testing for Sickle Cell Disease. Chris was instrumental in creating multiple business development partnerships and with engaging the investment community to achieve multiple rounds of financing for the company.

“Chris is an exceptional leader who is deeply committed to making a difference for people living with a rare disease,” said Onno Faber, Co-founder and CEO, Rarebase. “Over the last 18 months, we have uncovered potential treatments for hundreds of rare diseases, and have built a “drug-gene atlas” to enable AI-driven drug discovery. Having Chris in this new role puts us in the best position to accelerate growth and breakthrough advancements in the field of rare diseases.”

Moxham said, “I am honored to be assuming this new role. With a product engine designed to discover treatments for hundreds of monogenic diseases simultaneously, we are squarely focused on the largest untapped drug discovery opportunity in human health: rare diseases. I look forward to leading our world-class team of scientists, engineers, and operational leaders as we work tirelessly to improve the lives of everyone living with a rare disease.”