Financial StabilityNovo Nordisk is in-licensing the global rights to OMS-906 as part of a potential total $2.1B agreement, which includes a $240MM upfront payment that allows OMER to address near-term debt obligations and provides operational runway for over 12 months.
Market RecognitionPre-approval information exchanges with transplant centers, hospitals, and payers have been favorable, reflecting broad recognition of narsoplimab’s benefit-risk profile and dosing regimen.
Regulatory Approval ProcessOMER submitted a Marketing Authorization Application (MAA) to the European Medicines Agency (EMA) in June 2025, which has been validated and is now under review by the Committee for Medicinal Products for Human Use.