FDA Approval For Empaveli Marks Key Milestone In Apellis' Rare Disease Portfolio
1. FDA approved APLS Empaveli for C3G in patients aged 12 and older. 2. Empaveli showed a 68% reduction in proteinuria during VALIANT study. 3. Empaveli provides significant commercial potential, targeting 5,000 U.S. patients. 4. Analysts highlight concerns over competition impacting short-term stock performance. 5. APLS stock rose 0.88% to $18.92 following this positive news.