Biogen said it has paused or discontinued funding for most of Apellis' research programs as it integrates the $5.6 billion acquisition. The move raises near-term cash runway concerns for Apellis and could delay key programs, possibly pressuring valuation and investor sentiment ahead of any post-merger milestones.
Biogen has entered a definitive agreement to acquire Apellis for $41 per share, totaling $5.6 billion. This acquisition is expected to drive significant revenue growth from two immunology products, EMPAVELI and SYFOVRE, which collectively generated $689 million in revenue in 2025 and are projected to grow substantially through 2028.
Apellis Pharmaceuticals is experiencing significant growth with its rare kidney disease drug, Empaveli, prompting an upgrade from Bank of America that highlights an underappreciated opportunity in C3G. The positive early uptake, along with projected peak sales, suggests meaningful revenue potential in the coming years.
FDA approved APLS Empaveli for C3G in patients aged 12 and older. Empaveli showed a 68% reduction in proteinuria during VALIANT study. Empaveli provides significant commercial potential, targeting 5,000 U.S. patients. Analysts highlight concerns over competition impacting short-term stock performance. APLS stock rose 0.88% to $18.92 following this positive news.
FDA granted Priority Review for APLS's Empaveli for C3G and IC-MPGN. Phase 3 VALIANT results showed significant proteinuria reduction in treated patients. Empaveli achieved favorable safety profile consistent with established data. Market size for C3G could be larger post-approval of Empaveli. APLS stock rose 8.05% following the FDA news.
APLS reported a quarterly loss of 29 cents per share, beating estimates. Sales grew 45.2%, reaching $212.5 million, above consensus expectations. JP Morgan maintains an Overweight rating with a $54 price target. Syfovre sales totaled $167.8 million for the fourth quarter. Empaveli's market application could significantly boost APLS revenues in late 2025.