Swedish Orphan Biovitrum AB (Sobi) has received a positive opinion from the Committee for Medicinal Products for Human Use $(CHMP)$ of the European Medicines Agency for Aspaveli® (pegcetacoplan) as a treatment for adult and adolescent patients with C3 glomerulopathy (C3G) or primary immune-complex membranoproliferative glomerulonephritis (IC-MPGN). If approved by the European Commission, Aspaveli would become the first therapy for patients 12 years and older with these rare kidney diseases in Europe. Sobi and its partner Apellis Pharmaceuticals, Inc. have global co-development rights for systemic pegcetacoplan. The European Commission's decision is expected in the first quarter of 2026.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Swedish Orphan Biovitrum AB published the original content used to generate this news brief on December 12, 2025, and is solely responsible for the information contained therein.
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