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Apellis Pharmaceuticals, Inc. - Common Stock (APLS)

19.00
+0.00 (0.00%)
NASDAQ · Last Trade: Jul 31st, 9:07 AM EDT
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Detailed Quote

Previous Close19.00
Open-
Bid20.50
Ask20.72
Day's RangeN/A - N/A
52 Week Range16.10 - 41.94
Volume107,420
Market Cap2.21B
PE Ratio (TTM)-10.61
EPS (TTM)-1.8
Dividend & YieldN/A (N/A)
1 Month Average Volume2,357,481

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About Apellis Pharmaceuticals, Inc. - Common Stock (APLS)

Apellis Pharmaceuticals is a biopharmaceutical company focused on developing innovative therapies for the treatment of serious diseases through its expertise in complement biology. The company works on advancing its proprietary drug candidates designed to modulate the immune system, with particular attention to rare and complex conditions that currently have limited treatment options. By harnessing advanced science and technology, Apellis aims to improve patient outcomes and address unmet medical needs in various therapeutic areas, including hematology and ophthalmology. Read More

News & Press Releases

APELLIS PHARMACEUTICALS INC (NASDAQ:APLS) Reports Mixed Q2 2025 Results with EPS Beat and Revenue Misschartmill.com
Apellis Pharmaceuticals (APLS) reported mixed Q2 2025 results, missing revenue estimates ($178.49M vs. $192.29M) but beating EPS (-$0.33 vs. -$0.49). Shares rose 4.58% pre-market as FDA approval for EMPAVELI® boosts future prospects.
Via Chartmill · July 31, 2025
Apellis Pharmaceuticals Reports Second Quarter 2025 Financial Results
WALTHAM, Mass., July 31, 2025 (GLOBE NEWSWIRE) -- Apellis Pharmaceuticals, Inc. (Nasdaq: APLS), today announced its second quarter 2025 financial results and business highlights.
By Apellis Pharmaceuticals, Inc. · Via GlobeNewswire · July 31, 2025
Earnings Scheduled For July 31, 2025benzinga.com
Via Benzinga · July 31, 2025
FDA Approval For Empaveli Marks Key Milestone In Apellis' Rare Disease Portfoliobenzinga.com
FDA approves Apellis' Empaveli for rare kidney diseases, with trial data showing strong efficacy in reducing proteinuria and clearing C3 deposits.
Via Benzinga · July 29, 2025
Why Retail Investors Are Turning Sharply Bullish On Apellis Pharmaceuticalsstocktwits.com
The FDA approved Apellis’ drug Empaveli for two rare kidney diseases, following strong results from a Phase 3 trial.
Via Stocktwits · July 28, 2025
Earnings Scheduled For May 7, 2025benzinga.com
Via Benzinga · May 7, 2025
Apellis Pharmaceuticals's Earnings Outlookbenzinga.com
Via Benzinga · May 6, 2025
FDA Approves Apellis’ EMPAVELI® (pegcetacoplan) as the First C3G and Primary IC-MPGN Treatment for Patients 12 and Older
By Apellis Pharmaceuticals, Inc. · Via GlobeNewswire · July 28, 2025
Apellis Pharmaceuticals to Host Conference Call on July 31, 2025, to Discuss Second Quarter 2025 Financial Results
WALTHAM, Mass., July 24, 2025 (GLOBE NEWSWIRE) -- Apellis Pharmaceuticals, Inc. (Nasdaq: APLS) today announced that the company will host a conference call and webcast to discuss its second quarter 2025 financial results on Thursday, July 31, 2025, at 8:30 a.m. ET.
By Apellis Pharmaceuticals, Inc. · Via GlobeNewswire · July 24, 2025
Apellis Pharmaceuticals Stock: A Deep Dive Into Analyst Perspectives (15 Ratings)benzinga.com
Via Benzinga · July 18, 2025
Apellis Announces Five Abstracts Accepted for Oral Presentation at the American Society of Retina Specialists (ASRS) Annual Scientific Meeting
WALTHAM, Mass., July 15, 2025 (GLOBE NEWSWIRE) -- Apellis Pharmaceuticals, Inc. (Nasdaq: APLS) today announced that five abstracts were accepted for oral presentation at the American Society of Retina Specialists (ASRS) Annual Scientific Meeting to be held July 30 - August 2 in Long Beach, California. These data further demonstrate the robust efficacy and well-documented safety profile of SYFOVRE® (pegcetacoplan injection) for patients with geographic atrophy (GA) secondary to age-related macular degeneration (AMD).
By Apellis Pharmaceuticals, Inc. · Via GlobeNewswire · July 15, 2025
What 13 Analyst Ratings Have To Say About Apellis Pharmaceuticalsbenzinga.com
Via Benzinga · July 2, 2025
Apellis to Receive up to $300 Million from Royalty Purchase Agreement with Sobi for Ex-U.S. Royalties of Aspaveli® (systemic pegcetacoplan)
WALTHAM, Mass., July 01, 2025 (GLOBE NEWSWIRE) -- Apellis Pharmaceuticals, Inc. (Nasdaq: APLS) today announced a capped royalty purchase agreement with Sobi® under which Apellis will receive up to $300 million in exchange for 90% of Apellis’ future ex-U.S. royalties for Aspaveli® (systemic pegcetacoplan). Under the companies’ 2020 collaboration agreement, Apellis is eligible for tiered royalties on ex-U.S. sales of Aspaveli ranging from high teens to high twenties. Apellis retains exclusive commercialization rights for systemic pegcetacoplan in the United States, where the product is marketed as EMPAVELI®.
Apellis and Sobi Announce EMPAVELI® (pegcetacoplan) Showed Sustained Efficacy at One Year in Phase 3 Study for C3G and Primary IC-MPGN
WALTHAM, Mass. and STOCKHOLM, June 06, 2025 (GLOBE NEWSWIRE) -- Apellis Pharmaceuticals, Inc. (Nasdaq: APLS) and Sobi® (STO:SOBI) today presented new data from the open-label period of the Phase 3 VALIANT study, investigating EMPAVELI® (pegcetacoplan) for C3 glomerulopathy (C3G) and primary immune complex membranoproliferative glomerulonephritis (IC-MPGN). The data were presented as part of a late-breaking session at the European Renal Association (ERA) Congress.
Apellis Pharmaceuticals to Present at the Goldman Sachs 46th Annual Global Healthcare Conference
WALTHAM, Mass., June 04, 2025 (GLOBE NEWSWIRE) -- Apellis Pharmaceuticals, Inc. (Nasdaq: APLS) today announced that the company will present at the Goldman Sachs 46th Annual Global Healthcare Conference on Wednesday, June 11, 2025 at 10:40 a.m. ET.
Expert Outlook: Apellis Pharmaceuticals Through The Eyes Of 17 Analystsbenzinga.com
Via Benzinga · May 22, 2025
Why Apellis Pharmaceuticals Wilted on Wednesdayfool.com
Via The Motley Fool · May 7, 2025
Sarepta Therapeutics, Mercury Systems, Arista Networks And Other Big Stocks Moving Lower In Wednesday's Pre-Market Sessionbenzinga.com
Via Benzinga · May 7, 2025
Apellis Pharmaceuticals Reports First Quarter 2025 Financial Results
WALTHAM, Mass., May 07, 2025 (GLOBE NEWSWIRE) --  Apellis Pharmaceuticals, Inc. (Nasdaq: APLS), today announced its first quarter 2025 financial results and business highlights.
Apellis Pharmaceuticals to Present at Upcoming Investor Conferences
WALTHAM, Mass., May 06, 2025 (GLOBE NEWSWIRE) -- Apellis Pharmaceuticals, Inc. (Nasdaq: APLS) today announced that the company will participate in the following May investor conferences:
Apellis Pharmaceuticals to Host Conference Call on May 7, 2025, to Discuss First Quarter 2025 Financial Results
WALTHAM, Mass., April 30, 2025 (GLOBE NEWSWIRE) -- Apellis Pharmaceuticals, Inc. (Nasdaq: APLS) today announced that the company will host a conference call and webcast to discuss its first quarter 2025 financial results on Wednesday, May 7, 2025, at 8:30 a.m. ET.
By Apellis Pharmaceuticals, Inc. · Via GlobeNewswire · April 30, 2025
What 9 Analyst Ratings Have To Say About Apellis Pharmaceuticalsbenzinga.com
Via Benzinga · April 29, 2025
Apellis Announces Craig Wheeler to Join the Board of Directors
WALTHAM, Mass., April 21, 2025 (GLOBE NEWSWIRE) -- Apellis Pharmaceuticals, Inc. (Nasdaq: APLS) today announced that Craig Wheeler, founder and chief executive officer of Headwaters Biotech Advisors, will join the Apellis Board of Directors, effective immediately. Mr. Wheeler is a highly accomplished executive with more than 30 years of leadership experience across the biopharmaceutical industry.
By Apellis Pharmaceuticals, Inc. · Via GlobeNewswire · April 21, 2025
FDA Reviews Kidney Disease Drug From Apellis Pharmaceuticalsbenzinga.com
Apellis' Empaveli receives FDA Priority Review for rare kidney diseases C3G and IC-MPGN. Phase 3 data show strong efficacy in proteinuria reduction.
Via Benzinga · April 1, 2025
Apellis Announces FDA Acceptance and Priority Review of the Supplemental New Drug Application for EMPAVELI® (pegcetacoplan) for C3G and Primary IC-MPGN
WALTHAM, Mass., April 01, 2025 (GLOBE NEWSWIRE) -- Apellis Pharmaceuticals, Inc. (Nasdaq: APLS) today announced that the U.S. Food and Drug Administration (FDA) has accepted and granted Priority Review designation of the supplemental New Drug Application (sNDA) for EMPAVELI® (pegcetacoplan) for C3 glomerulopathy (C3G) and primary immune complex membranoproliferative glomerulonephritis (IC-MPGN), which are severe and rare kidney diseases. The Prescription Drug User Fee Act (PDUFA) target action date is July 28, 2025.
By Apellis Pharmaceuticals, Inc. · Via GlobeNewswire · April 1, 2025