John Glasspool is CEO and member of the Board of Directors of Anthos Therapeutics. Prior to joining Anthos, Mr. Glasspool served in a number of roles at Novartis Pharma, including Global Head of Cardiovascular & Metabolism Business Franchise.
Describe abelacimab’s latest Phase 2 trial. How did the treatment perform?
John Glasspool: This study covered over 1,200 patients with atrial fibrillation, or an irregular heartbeat – a condition that affects 37 million people worldwide and puts them at moderate-to-high risk of stroke. This was the largest and longest study of its kind, and it showed a highly significant reduction in bleeding with abelacimab compared to a standard-of-care blood thinner, a direct-oral anticoagulant (DOAC).
Why are these findings significant in the landscape of antithrombotic treatments?
JG: We see this as a landmark study and, if approved, a transformational moment for patients. The risk of bleeding – or the fear of it – prevents many patients from living in optimal health, limiting their usual activities. By separating “good” clotting from “bad” clotting, abelacimab would allow these patients to receive the care they need and open up the door to healthier, more active lifestyles.
What’s next for Anthos?
JG: With Blackstone’s support, we’ll be able to continue the exciting development of abelacimab in Phase 3 studies which are currently underway across the world, with the hope to get it to patients.