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Revenue
Apellis’s total revenue surged 133.0% year-over-year to $458.58 million in Q3 2025, driven by a $280.82 million licensing and other revenue segment, which dwarfed the $177.75 million in product revenue. The licensing component, reflecting partnerships and milestone payments, underscored the company’s strategic shift toward diversified revenue streams. Product revenue, though lower in proportion, demonstrated resilience, with SYFOVRE contributing $150.93 million and EMPAVELI adding $26.83 million.
Earnings/Net Income
The company achieved a dramatic turnaround, reporting a net income of $215.72 million in Q3 2025, a 475.5% increase from a $57.45 million net loss in the prior-year period. EPS jumped to $1.71 from a $0.46 loss, marking a 471.7% improvement. This reversal highlights effective cost management and licensing-driven profitability, though the company has historically faced multi-year losses in this quarter.
Post-Earnings Price Action Review
Despite the positive earnings report, Apellis’s stock price experienced significant post-earnings volatility. Shares plummeted 16.58% on the latest trading day, 27.54% over the prior week, and 8.40% month-to-date. The sharp decline contrasts with the company’s strong financial performance, suggesting market skepticism about sustainability or broader sector pressures. Analysts attributed the drop to concerns over operational challenges, including manufacturing delays and slow adoption rates for complement inhibitors in geographic atrophy.
CEO Commentary
John Orwin, CEO of
Guidance
Apellis raised its 2026 revenue guidance to $550-570 million, up from prior estimates, with EPS expected to reach $2.10-2.25. The company also aims to file a Biologics License Application for a new indication by mid-2026 and will maintain R&D investment at 30-35% of revenue.
Additional News
Recent non-earnings developments include FDA approval for Mpati, expanding treatment access for 5,000 patients with C3 glomerulopathy. The company also announced a $275 million upfront payment from Sobi and launched AI tools to enhance geographic atrophy treatment. Additionally, Apellis transitioned to prefilled syringes for SYFOVRE, aiming to improve physician adoption.
<img src="https://cdn.ainvest.com/aigc/hxcmp/images/compress-aime_generated_1761911661016.jpg.png" style="max-width:100%;">
Key Non-Earnings Developments
1. Product Expansion: FDA approval of Mpati for C3 glomerulopathy and primary immune complex membranoproliferative glomerulonephritis, broadening Apellis’s patient reach.
2. Strategic Partnerships: A $275 million licensing deal with Sobi, boosting non-product revenue.
3. Operational Innovations: Development of AI tools and prefilled syringes to address geographic atrophy challenges and streamline administration.
Article Polishing
The article has been refined for clarity, flow, and consistency, with enhanced transitions between sections and updated punctuation. All numerical data and factual claims remain unchanged, adhering to the original structure and emphasis on key financial and strategic metrics.
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