Overview
- Novo obtains exclusive global rights to develop and commercialize zaltenibart for rare blood and kidney disorders.
- Deal terms include $340 million in upfront and near-term milestone payments, with up to $2.1 billion in total potential payouts plus sales royalties.
- The transaction is expected to close in the fourth quarter of 2025, after which Novo plans to launch a global Phase 3 program in paroxysmal nocturnal hemoglobinuria and to evaluate other indications.
- Company statements report the MASP-3 inhibitor was safe and well tolerated in testing and may offer advantages over other alternative-pathway therapies.
- Omeros retains certain preclinical MASP-3 rights, is seeking this-quarter approval of narsoplimab for transplant-associated thrombotic microangiopathy, and saw its shares nearly triple on the news.