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NASDAQ:APLS

Apellis Pharmaceuticals Q2 2025 Earnings Report

Apellis Pharmaceuticals logo
$19.44 -0.09 (-0.46%)
Closing price 07/11/2025 04:00 PM Eastern
Extended Trading
$19.31 -0.13 (-0.67%)
As of 07/11/2025 05:50 PM Eastern
Extended trading is trading that happens on electronic markets outside of regular trading hours. This is a fair market value extended hours price provided by Polygon.io. Learn more.

Apellis Pharmaceuticals EPS Results

Actual EPS
N/A
Consensus EPS
-$0.44
Beat/Miss
N/A
One Year Ago EPS
N/A

Apellis Pharmaceuticals Revenue Results

Actual Revenue
N/A
Expected Revenue
N/A
Beat/Miss
N/A
YoY Revenue Growth
N/A

Apellis Pharmaceuticals Announcement Details

Quarter
Q2 2025
Time
Before Market Opens
Conference Call Date
Thursday, July 31, 2025
Conference Call Time
8:30AM ET

Conference Call Resources

Apellis Pharmaceuticals Earnings Headlines

A grave, grave error.
I thought what happened 25 years ago was a once- in-a-lifetime event… but how wrong I was. Because here we are, a quarter of a century later, almost to the exact day, and it’s happening again.
William Blair Has Positive Forecast for APLS Q3 Earnings
Wedbush Issues Optimistic Outlook for APLS Earnings
See More Apellis Pharmaceuticals Headlines
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About Apellis Pharmaceuticals

Apellis Pharmaceuticals (NASDAQ:APLS) is a clinical‐stage biopharmaceutical company headquartered in Waltham, Massachusetts, dedicated to the discovery, development and commercialization of novel therapeutic compounds that target the complement system. Since its founding in 2009, Apellis has built a proprietary platform centered on compstatin‐based C3 inhibitors, aiming to address serious and rare diseases driven by dysregulation of the complement cascade. The company completed its initial public offering on the NASDAQ in 2014 and has since advanced multiple candidates through regulatory review and clinical trials.

Apellis’s lead product, pegcetacoplan—commercialized under the trade name Empaveli in paroxysmal nocturnal hemoglobinuria (PNH) and Syfovre for geographic atrophy (GA) secondary to age-related macular degeneration—represents the first systemic C3 inhibitor approved for clinical use. The company’s pipeline also includes investigational assets such as APL-9, APL-2 and other next‐generation molecules targeting additional complement‐mediated conditions, including cold agglutinin disease, C3 glomerulopathies and chronic inflammatory disorders. Apellis conducts multinational clinical studies and has secured regulatory authorizations in major markets across North America, Europe and Asia.

Beyond its clinical programs, Apellis collaborates with strategic partners to enhance its global reach and accelerate development timelines. Collaborations with leading ophthalmology and hematology organizations have enabled joint research initiatives, manufacturing scale-up and commercialization efforts. The company’s research and development operations leverage an integrated approach, combining translational science, biomarker analysis and patient‐focused trial designs to optimize safety and efficacy outcomes.

Under the leadership of Chief Executive Officer Cedric François, Apellis has expanded its executive team to include experienced professionals in regulatory affairs, clinical development and commercial operations. The board of directors comprises industry veterans and medical experts who guide corporate strategy and governance. Apellis remains committed to advancing therapies for underserved patient populations, with a mission to transform the treatment landscape for complement‐driven diseases worldwide.

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