Max Denning, MD, MBA
Max Denning leads the global diabetes development program for orforglipron, the first non-peptide oral GLP-1 receptor agonist to successfully complete multiple Phase 3 trials. Unlike currently available peptide based GLP-1 therapies, orforglipron can be taken orally, at any time of day, and without food or water restrictions—addressing both patient convenience and manufacturing scalability challenges facing the GLP-1 class. The ACHIEVE program has enrolled over 6,000 participants globally, with regulatory submissions anticipated in 2026.
Through Lilly's Accelerated R&D Leadership Program, prior to his current role, Max has worked across regulatory affairs, patient safety, and clinical development, giving him a comprehensive view of how innovative therapies navigate from lab to patient.
Max holds an MD from Oxford, an MSc in Patient Safety from Imperial College London, and an MBA from Stanford, where he was a Knight-Hennessy Scholar.