Overview
- Novo gains exclusive global rights to develop and commercialize zaltenibart for rare blood and kidney diseases, with additional milestones and royalties possible.
- Zaltenibart blocks MASP-3 to curb the alternative complement pathway, a different approach from current complement inhibitors on the market.
- The companies expect the transaction to close in the fourth quarter of 2025, after which Novo plans to launch a global Phase 3 program in paroxysmal nocturnal hemoglobinuria.
- Omeros retains certain preclinical MASP-3 assets unrelated to zaltenibart, including the option to pursue small‑molecule inhibitors under limited restrictions.
- Omeros shares jumped more than 150% on the announcement, as investors also look to an FDA decision on the company’s separate drug narsoplimab due December 26, 2025.