Developer docs
API playgroundTry for free, no card

Search company profiles

Apellis Pharmaceuticals

Full company profile

uuid00037n2

Namestring
Apellis Pharmaceuticals
Legal namestring
Apellis Pharmaceuticals, Inc.
Websiteurl
apellis.com
Company typeenum
Private
Founded yearint
2009
Descriptiontext

Apellis Pharmaceuticals is a biopharmaceutical company that developed and commercialized pegcetacoplan, the first and only approved C3 inhibitor and the first new class of complement medicine in approximately 15 years. The company's core technology targets C3, the central protein of the complement cascade and the only target that addresses all three activation pathways (classical, lectin, and alternative), enabling comprehensive control of complement-driven diseases. Apellis translates this single molecule into two FDA-approved products administered by different routes — EMPAVELI (subcutaneous) for paroxysmal nocturnal hemoglobinuria, C3 glomerulopathy, and primary immune-complex membranoproliferative glomerulonephritis, and SYFOVRE (intravitreal) for geographic atrophy secondary to age-related macular degeneration.

The company generates revenue primarily through U.S. specialty-pharmacy distribution of EMPAVELI and SYFOVRE to three prescriber segments: retina specialists and ophthalmologists (for SYFOVRE), and hematologists and nephrologists (for EMPAVELI). SYFOVRE generated $587M in FY2025 product revenue with ~102,000 doses delivered and 60% market share in geographic atrophy, while EMPAVELI generated $102M with over 5% penetration of the U.S. C3G/IC-MPGN patient population in its first full quarter post-launch. Ex-U.S. rights for systemic pegcetacoplan are held by Sobi under a co-development and commercialization agreement, which generated a $275M royalty repurchase payment to Apellis in 2025. The company was acquired by Biogen Inc. on May 14, 2026 for approximately $5.6 billion ($41 per share plus contingent value rights), at which point Apellis became a wholly owned subsidiary integrated into Biogen's commercial infrastructure.

Short descriptiontext

Apellis Pharmaceuticals develops and commercializes pegcetacoplan, the first approved C3 inhibitor, delivered as EMPAVELI (subcutaneous) for PNH and rare kidney diseases and SYFOVRE (intravitreal) for geographic atrophy. The company was acquired by Biogen in May 2026 for approximately $5.6 billion.

Operating statusenum
Acquired
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersWaltham, United States
HQ citystring
Waltham
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices5 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
complement therapeutics, rare disease drugs, C3 inhibitors, biopharmaceutical products, ophthalmic therapeutics
Industry1 code
1Plasma-Derived Protease Inhibitors & Complement Modulators (e.g., C1 Esterase Inhibitor)
CodeHLAIAHAFPrimaryYes
NAICS code1 code
  • Medical and Diagnostic Laboratories62151
SIC code1 code
  • Wholesale-Drugs, Proprietaries & Druggists' Sundries5122
Product category
Complement Therapeutics
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model4 records
1EMPAVELI (pegcetacoplan) - U.S. Product Sales
TypeOne Time License
Description

EMPAVELI generated $35.1 million in Q4 2025 net product revenue, up 50% year-over-year, and $102 million for full-year 2025. It is approved for paroxysmal nocturnal hemoglobinuria (PNH) and C3 glomerulopathy (C3G) / primary IC-MPGN. Apellis holds U.S. commercialization rights; Sobi holds ex-U.S. commercialization rights.

investing.com
2SYFOVRE (pegcetacoplan injection) - U.S. Product Sales
TypeOne Time License
Description

SYFOVRE generated $155.2 million in Q4 2025 U.S. net product revenue and $587 million for full-year 2025, with approximately 102,000 doses delivered and a 60% market share in geographic atrophy. SYFOVRE is the first-ever approved therapy for geographic atrophy.

investing.com
3Sobi Royalty and Co-development Agreement
TypeLicensing Royalties
Description

Sobi holds global co-development and ex-U.S. commercialization rights for systemic pegcetacoplan. Apellis received a $275 million upfront payment from Sobi's royalty repurchase in 2025 and up to $300 million through a royalty agreement. Sobi also secured Health Canada approval for EMPAVELI in C3G and primary IC-MPGN.

openpr.com
4Sixth Street Credit Facility
TypeTransaction Fee
Description

In May 2024, Apellis secured a $475 million non-dilutive senior secured credit facility from Sixth Street ($375 million funded at close), using most proceeds to buy out SFJ Pharmaceuticals' development liability, improving liquidity and reducing future payment obligations.

ca.marketscreener.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components4 values
Technology or R&D, Marketing or Sales, Operations, Personnel
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 4 records shown
1EMPAVELI
Description

Pegcetacoplan injection for subcutaneous use, approved for PNH and C3G/IC-MPGN

apellis.com
+3 more records
Core offering1 text field

Apellis develops and commercializes pegcetacoplan-based, C3-targeted therapeutics. EMPAVELI (pegcetacoplan subcutaneous injection) is approved for paroxysmal nocturnal hemoglobinuria (PNH), C3 glomerulopathy (C3G), and primary IC-MPGN. SYFOVRE (pegcetacoplan intravitreal injection) is the first-ever approved therapy for geographic atrophy (GA) secondary to age-related macular degeneration. The company also advances pipeline programs including combination therapies and gene-edited complement medicines via collaboration with Beam Therapeutics.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • SYFOVRE generated $587M in FY2025 revenue with approximately 102,000 doses delivered and 60% market share in geographic atrophy
+4 more records
Product overview1 text field

Apellis Pharmaceuticals is a biopharmaceutical company that developed two first-in-class C3-targeted medicines approved across four diseases. The company's portfolio consists of EMPAVELI (pegcetacoplan) for paroxysmal nocturnal hemoglobinuria (PNH), C3 glomerulopathy (C3G), and primary immune complex membranoproliferative glomerulonephritis (IC-MPGN), and SYFOVRE (pegcetacoplan injection) for geographic atrophy (GA) secondary to age-related macular degeneration. Both products are supported by patient assistance programs (EMPAVELI APELLIS ASSIST and SYFOVRE APELLIS ASSIST). The company was acquired by Biogen in May 2026.

Product and service2 records
1EMPAVELI (pegcetacoplan)
CategoryPrescription Drug — Complement Inhibitor
Description

EMPAVELI is a subcutaneous C3-targeted therapy approved for Paroxysmal Nocturnal Hemoglobinuria (PNH), C3 Glomerulopathy (C3G), and Primary Immune Complex Membranoproliferative Glomerulonephritis (IC-MPGN). It is the first new class of complement medicine in nearly 15 years and is prescribed by hematologists and nephrologists.

2SYFOVRE (pegcetacoplan injection)
CategoryPrescription Drug — Complement Inhibitor
Description

SYFOVRE is an intravitreal C3 inhibitor injection approved for Geographic Atrophy (GA) secondary to age-related macular degeneration. It is the first-ever approved therapy for geographic atrophy, a leading cause of blindness worldwide, and is administered by retina specialists and ophthalmologists.

Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-06-01
Description

Sobi holds global co-development and ex-U.S. commercialization rights for systemic pegcetacoplan (EMPAVELI). Sobi received Health Canada approval for EMPAVELI in C3G and primary IC-MPGN in 2026 and presented Phase 3 VALIANT data at ERA 2026. Sobi repurchased royalties from Apellis for a $275M upfront payment in 2025, and Apellis may receive up to $300M through a royalty agreement. Sobi also holds exclusive ex-U.S. commercialization rights for the VALIANT long-term extension (VALE) study.

Strategic tierCoreTypeOthersAnnounced on2026-03-31
Description

Biogen acquired Apellis Pharmaceuticals for approximately $5.6 billion ($41 per share in cash plus contingent value rights tied to SYFOVRE sales milestones). The acquisition was completed on May 14, 2026, with approximately 82.4% of outstanding shares tendered. Apellis became a wholly owned subsidiary of Biogen, adding two FDA-approved products (EMPAVELI and SYFOVRE) generating $689 million in combined net product revenue in 2025. The deal was expected to be accretive to Biogen's non-GAAP diluted EPS starting in 2027 and to deliver mid-to-high teens revenue growth through 2028.

Strategic tierCoreTypeOthersAnnounced on2026-03-31
Description

Biogen's acquisition adds two commercial complement-targeting therapies: SYFOVRE for geographic atrophy (ophthalmology) and EMPAVELI for complement-mediated diseases (hematology/nephrology). The deal strengthens Biogen's immunology and rare disease portfolio and expands capabilities in nephrology ahead of the planned launch of felzartamab, which Apellis's nephrology team will support.

Strategic tierStrategicTypeStrategic or Co-development PartnerAnnounced on2026-03-21
Description

Apellis entered into an exclusive research collaboration with Beam Therapeutics to discover novel base-edited treatments focused on complement targets in the eye, liver, and brain. The collaboration explores gene-edited complement therapies (APL-9099: gene-edited FcRn therapy) and oral complement inhibitors, extending Apellis's complement platform into gene editing and new therapeutic areas.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Alexion's Soliris and Ultomiris are C5 inhibitors for PNH and aHUS and directly compete with EMPAVELI in PNH; they set the incumbent standard of care that pegcetacoplan must displace, making Alexion Apellis's most direct competitor in complement-mediated rare disease.

TypeDirect peer
Description

Iveric Bio developed Izervay (avacincaptad pegol), a complement C5 inhibitor approved for geographic atrophy, directly competing with SYFOVRE in the same indication, prescribers, and patient population.

TypeBroad incumbent
Description

Regeneron's EYLEA franchise anchors the retinal disease market and competes for retina specialist mindshare and formulary positioning that SYFOVRE relies on for uptake, making it a broad incumbent ophthalmology peer.

TypeBroad incumbent
Description

Roche markets Vabysmo (faricimab) and historically Lucentis in retinal disease and ophthalmology, representing a broad incumbent competitor for SYFOVRE in retina specialist practices and payer negotiations.

TypeDirect peer
Description

BioMarin is a rare-disease biopharma commercializing enzyme-replacement and gene therapies for small patient populations, mirroring Apellis's specialty/rare-disease model across PNH, C3G/IC-MPGN, and GA.

TypeDirect peer
Description

Alnylam commercializes RNA-based therapeutics for rare diseases such as hATTR amyloidosis and primary hyperoxaluria using a specialty sales model similar to Apellis's APELLIS ASSIST programs, and shares several board and executive alumni.

TypeBroad incumbent
Description

Vertex is a high-margin rare-disease and specialty biopharma (cystic fibrosis, sickle cell, pain) with a comparable commercial model around specialty prescribers and rare-disease patient identification, positioning it as a peer in commercial sophistication and profitability profile.

TypeDirect peer
Description

Sobi is Apellis's global co-development and ex-U.S. commercialization partner for systemic pegcetacoplan (EMPAVELI) and also operates a complementary rare-disease hematology and immunology franchise, making it both a strategic partner and a comparable rare-disease commercial peer.

TypeBroad incumbent
Description

Takeda operates a broad rare-disease, hematology, and immunology portfolio across PNH-adjacent indications, with a global specialty commercial infrastructure similar in scale to Biogen's post-acquisition footprint for Apellis.

TypeEmerging player
Description

Beam is Apellis's research collaborator on base-edited complement therapies (eye, liver, brain) and represents an emerging modality peer exploring gene-editing approaches against complement and adjacent targets.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment4 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles17 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds13 records

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors20 records

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A1 record

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Apellis Pharmaceuticals

Complement Therapeuticsapellis.com

Apellis Pharmaceuticals develops and commercializes pegcetacoplan, the first approved C3 inhibitor, delivered as EMPAVELI (subcutaneous) for PNH and rare kidney diseases and SYFOVRE (intravitreal) for geographic atrophy. The company was acquired by Biogen in May 2026 for approximately $5.6 billion.

What Apellis Pharmaceuticals does

Apellis Pharmaceuticals is a biopharmaceutical company that developed and commercialized pegcetacoplan, the first and only approved C3 inhibitor and the first new class of complement medicine in approximately 15 years. The company's core technology targets C3, the central protein of the complement cascade and the only target that addresses all three activation pathways (classical, lectin, and alternative), enabling comprehensive control of complement-driven diseases. Apellis translates this single molecule into two FDA-approved products administered by different routes — EMPAVELI (subcutaneous) for paroxysmal nocturnal hemoglobinuria, C3 glomerulopathy, and primary immune-complex membranoproliferative glomerulonephritis, and SYFOVRE (intravitreal) for geographic atrophy secondary to age-related macular degeneration.

The company generates revenue primarily through U.S. specialty-pharmacy distribution of EMPAVELI and SYFOVRE to three prescriber segments: retina specialists and ophthalmologists (for SYFOVRE), and hematologists and nephrologists (for EMPAVELI). SYFOVRE generated $587M in FY2025 product revenue with ~102,000 doses delivered and 60% market share in geographic atrophy, while EMPAVELI generated $102M with over 5% penetration of the U.S. C3G/IC-MPGN patient population in its first full quarter post-launch. Ex-U.S. rights for systemic pegcetacoplan are held by Sobi under a co-development and commercialization agreement, which generated a $275M royalty repurchase payment to Apellis in 2025. The company was acquired by Biogen Inc. on May 14, 2026 for approximately $5.6 billion ($41 per share plus contingent value rights), at which point Apellis became a wholly owned subsidiary integrated into Biogen's commercial infrastructure.

Apellis Pharmaceuticals firmographics

Firmographics
Name
Apellis Pharmaceuticals
Legal name
Apellis Pharmaceuticals, Inc.
Website
https://apellis.com
Company type
Private
Founded year
2009
Operating status
Acquired
Headcount range
501–1,000 employees
Short description
Apellis Pharmaceuticals develops and commercializes pegcetacoplan, the first approved C3 inhibitor, delivered as EMPAVELI (subcutaneous) for PNH and rare kidney diseases and SYFOVRE (intravitreal) for geographic atrophy. The company was acquired by Biogen in May 2026 for approximately $5.6 billion.
Ownership category
akta.pro rank

Apellis Pharmaceuticals industry classification

Industry
Product category
Complement Therapeutics
NAICS
Medical and Diagnostic Laboratories (62151)
SIC
Wholesale-Drugs, Proprietaries & Druggists' Sundries (5122)
akta.pro primary industry
Plasma-Derived Protease Inhibitors & Complement Modulators (e.g., C1 Esterase Inhibitor) (HLAIAHAF)

Keywords

  • Complement therapeutics
  • Rare disease drugs
  • C3 inhibitors
  • Biopharmaceutical products
  • Ophthalmic therapeutics

Where Apellis Pharmaceuticals is headquartered

Location

Headquarters

HQ city
Waltham
HQ country
United States
HQ region
North America

Offices5 records

Markets served

Apellis Pharmaceuticals business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Marketing or Sales, Operations, Personnel

Revenue model

  1. EMPAVELI (pegcetacoplan) - U.S. Product Sales: EMPAVELI generated $35.1 million in Q4 2025 net product revenue, up 50% year-over-year, and $102 million for full-year 2025. It is approved for paroxysmal nocturnal hemoglobinuria (PNH) and C3 glomerulopathy (C3G) / primary IC-MPGN. Apellis holds U.S. commercialization rights; Sobi holds ex-U.S. commercialization rights.
  2. SYFOVRE (pegcetacoplan injection) - U.S. Product Sales: SYFOVRE generated $155.2 million in Q4 2025 U.S. net product revenue and $587 million for full-year 2025, with approximately 102,000 doses delivered and a 60% market share in geographic atrophy. SYFOVRE is the first-ever approved therapy for geographic atrophy.
  3. Sobi Royalty and Co-development Agreement: Sobi holds global co-development and ex-U.S. commercialization rights for systemic pegcetacoplan. Apellis received a $275 million upfront payment from Sobi's royalty repurchase in 2025 and up to $300 million through a royalty agreement. Sobi also secured Health Canada approval for EMPAVELI in C3G and primary IC-MPGN.
  4. Sixth Street Credit Facility: In May 2024, Apellis secured a $475 million non-dilutive senior secured credit facility from Sixth Street ($375 million funded at close), using most proceeds to buy out SFJ Pharmaceuticals' development liability, improving liquidity and reducing future payment obligations.

Go-to-market motion2 records

Distribution channels1 record

Marketing channels6 records

Apellis Pharmaceuticals product offering

Product offering

Core offering

Apellis develops and commercializes pegcetacoplan-based, C3-targeted therapeutics. EMPAVELI (pegcetacoplan subcutaneous injection) is approved for paroxysmal nocturnal hemoglobinuria (PNH), C3 glomerulopathy (C3G), and primary IC-MPGN. SYFOVRE (pegcetacoplan intravitreal injection) is the first-ever approved therapy for geographic atrophy (GA) secondary to age-related macular degeneration. The company also advances pipeline programs including combination therapies and gene-edited complement medicines via collaboration with Beam Therapeutics.

Product overview

Apellis Pharmaceuticals is a biopharmaceutical company that developed two first-in-class C3-targeted medicines approved across four diseases. The company's portfolio consists of EMPAVELI (pegcetacoplan) for paroxysmal nocturnal hemoglobinuria (PNH), C3 glomerulopathy (C3G), and primary immune complex membranoproliferative glomerulonephritis (IC-MPGN), and SYFOVRE (pegcetacoplan injection) for geographic atrophy (GA) secondary to age-related macular degeneration. Both products are supported by patient assistance programs (EMPAVELI APELLIS ASSIST and SYFOVRE APELLIS ASSIST). The company was acquired by Biogen in May 2026.

Differentiator

Problem solved

Functional benefit

Brands

  • EMPAVELI: Pegcetacoplan injection for subcutaneous use, approved for PNH and C3G/IC-MPGN
  • SYFOVRE
  • EMPAVELI APELLIS ASSIST
  • SYFOVRE APELLIS ASSIST

Products and services

  • EMPAVELI (pegcetacoplan) EMPAVELI is a subcutaneous C3-targeted therapy approved for Paroxysmal Nocturnal Hemoglobinuria (PNH), C3 Glomerulopathy (C3G), and Primary Immune Complex Membranoproliferative Glomerulonephritis (IC-MPGN). It is the first new class of complement medicine in nearly 15 years and is prescribed by hematologists and nephrologists.
  • SYFOVRE (pegcetacoplan injection) SYFOVRE is an intravitreal C3 inhibitor injection approved for Geographic Atrophy (GA) secondary to age-related macular degeneration. It is the first-ever approved therapy for geographic atrophy, a leading cause of blindness worldwide, and is administered by retina specialists and ophthalmologists.

Quantifiable outcome

  • SYFOVRE generated $587M in FY2025 revenue with approximately 102,000 doses delivered and 60% market share in geographic atrophy
  • +4 more outcomes

Companies that use Apellis Pharmaceuticals

Customer profile

Named customers3 records

Segments4 records

Ideal customer profiles3 records

Apellis Pharmaceuticals technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Apellis Pharmaceuticals partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and strategic.

  • Sobi (Swedish Orphan Biovitrum)coreStrategic or Co-development Partner · 1 June 2026Sobi holds global co-development and ex-U.S. commercialization rights for systemic pegcetacoplan (EMPAVELI). Sobi received Health Canada approval for EMPAVELI in C3G and primary IC-MPGN in 2026 and presented Phase 3 VALIANT data at ERA 2026. Sobi repurchased royalties from Apellis for a $275M upfront payment in 2025, and Apellis may receive up to $300M through a royalty agreement. Sobi also holds exclusive ex-U.S. commercialization rights for the VALIANT long-term extension (VALE) study.
  • Biogen Inc.coreOthers · 31 March 2026Biogen acquired Apellis Pharmaceuticals for approximately $5.6 billion ($41 per share in cash plus contingent value rights tied to SYFOVRE sales milestones). The acquisition was completed on May 14, 2026, with approximately 82.4% of outstanding shares tendered. Apellis became a wholly owned subsidiary of Biogen, adding two FDA-approved products (EMPAVELI and SYFOVRE) generating $689 million in combined net product revenue in 2025. The deal was expected to be accretive to Biogen's non-GAAP diluted EPS starting in 2027 and to deliver mid-to-high teens revenue growth through 2028.
  • Biogen Inc.coreOthers · 31 March 2026Biogen's acquisition adds two commercial complement-targeting therapies: SYFOVRE for geographic atrophy (ophthalmology) and EMPAVELI for complement-mediated diseases (hematology/nephrology). The deal strengthens Biogen's immunology and rare disease portfolio and expands capabilities in nephrology ahead of the planned launch of felzartamab, which Apellis's nephrology team will support.
  • Beam TherapeuticsstrategicStrategic or Co-development Partner · 21 March 2026Apellis entered into an exclusive research collaboration with Beam Therapeutics to discover novel base-edited treatments focused on complement targets in the eye, liver, and brain. The collaboration explores gene-edited complement therapies (APL-9099: gene-edited FcRn therapy) and oral complement inhibitors, extending Apellis's complement platform into gene editing and new therapeutic areas.

Scale indicators9 records

Recent moves6 records

Expansion highlights6 records

Apellis Pharmaceuticals competitors and assessment

Company assessment

Direct peers

  • Alexion (AstraZeneca): Alexion's Soliris and Ultomiris are C5 inhibitors for PNH and aHUS and directly compete with EMPAVELI in PNH; they set the incumbent standard of care that pegcetacoplan must displace, making Alexion Apellis's most direct competitor in complement-mediated rare disease.
  • Iveric Bio (Astellas): Iveric Bio developed Izervay (avacincaptad pegol), a complement C5 inhibitor approved for geographic atrophy, directly competing with SYFOVRE in the same indication, prescribers, and patient population.
  • BioMarin Pharmaceutical: BioMarin is a rare-disease biopharma commercializing enzyme-replacement and gene therapies for small patient populations, mirroring Apellis's specialty/rare-disease model across PNH, C3G/IC-MPGN, and GA.
  • Alnylam Pharmaceuticals: Alnylam commercializes RNA-based therapeutics for rare diseases such as hATTR amyloidosis and primary hyperoxaluria using a specialty sales model similar to Apellis's APELLIS ASSIST programs, and shares several board and executive alumni.
  • Swedish Orphan Biovitrum (Sobi): Sobi is Apellis's global co-development and ex-U.S. commercialization partner for systemic pegcetacoplan (EMPAVELI) and also operates a complementary rare-disease hematology and immunology franchise, making it both a strategic partner and a comparable rare-disease commercial peer.

Broad incumbents

  • Regeneron Pharmaceuticals: Regeneron's EYLEA franchise anchors the retinal disease market and competes for retina specialist mindshare and formulary positioning that SYFOVRE relies on for uptake, making it a broad incumbent ophthalmology peer.
  • Roche / Genentech: Roche markets Vabysmo (faricimab) and historically Lucentis in retinal disease and ophthalmology, representing a broad incumbent competitor for SYFOVRE in retina specialist practices and payer negotiations.
  • Vertex Pharmaceuticals: Vertex is a high-margin rare-disease and specialty biopharma (cystic fibrosis, sickle cell, pain) with a comparable commercial model around specialty prescribers and rare-disease patient identification, positioning it as a peer in commercial sophistication and profitability profile.
  • Takeda Pharmaceutical: Takeda operates a broad rare-disease, hematology, and immunology portfolio across PNH-adjacent indications, with a global specialty commercial infrastructure similar in scale to Biogen's post-acquisition footprint for Apellis.

Emerging players

  • Beam Therapeutics: Beam is Apellis's research collaborator on base-edited complement therapies (eye, liver, brain) and represents an emerging modality peer exploring gene-editing approaches against complement and adjacent targets.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks5 records

Key highlights7 records

Customer concentration

Apellis Pharmaceuticals social profiles

Digital presence

Apellis Pharmaceuticals financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Apellis Pharmaceuticals leadership team

Management profile

Number of profiles

Profiles17 records

Apellis Pharmaceuticals funding detail

Funding detail

Funding overview

Funding rounds13 records

Investors20 records

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Apellis Pharmaceuticals M&A and investment

M&A and investment

M&A1 record

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Apellis Pharmaceuticals

What does Apellis Pharmaceuticals do?

Apellis develops and commercializes pegcetacoplan-based, C3-targeted therapeutics. EMPAVELI (pegcetacoplan subcutaneous injection) is approved for paroxysmal nocturnal hemoglobinuria (PNH), C3 glomerulopathy (C3G), and primary IC-MPGN. SYFOVRE (pegcetacoplan intravitreal injection) is the first-ever approved therapy for geographic atrophy (GA) secondary to age-related macular degeneration. The company also advances pipeline programs including combination therapies and gene-edited complement medicines via collaboration with Beam Therapeutics.

Is Apellis Pharmaceuticals a public or private company?

Apellis Pharmaceuticals is a private company. It is classified as corporate owned and is currently acquired.

When was Apellis Pharmaceuticals founded?

Apellis Pharmaceuticals was founded in 2009. It employs 501 to 1,000 people.

Where is Apellis Pharmaceuticals based?

Apellis Pharmaceuticals is headquartered in Waltham, United States, in the North America region.

How does Apellis Pharmaceuticals make money?

Four revenue lines are on record. EMPAVELI (pegcetacoplan) - U.S. Product Sales are the primary driver. The others are SYFOVRE (pegcetacoplan injection) - U.S. Product Sales, sobi Royalty and Co-development Agreement and sixth Street Credit Facility.

Who are Apellis Pharmaceuticals's main competitors?

Direct peers on record are Alexion (AstraZeneca), Iveric Bio (Astellas), BioMarin Pharmaceutical, Alnylam Pharmaceuticals and Swedish Orphan Biovitrum (Sobi). Broad incumbents are Regeneron Pharmaceuticals, Roche / Genentech, Vertex Pharmaceuticals and Takeda Pharmaceutical. Beam Therapeutics is listed as an emerging player.

Does Apellis Pharmaceuticals have an API?

No public API is recorded for Apellis Pharmaceuticals.

What industry is Apellis Pharmaceuticals in?

Apellis Pharmaceuticals's product category is Complement Therapeutics. Its primary akta.pro industry code is HLAIAHAF, Plasma-Derived Protease Inhibitors & Complement Modulators (e.g., C1 Esterase Inhibitor). Its NAICS code is 62151 and its SIC code is 5122.

Unlock the full company data

50 free credits on sign-up, no credit card required.

Contact sales
Live signals
TradingViewNews by Dow Jones Newswires on TradingView, 2026-09-26Biotech stocks surged this year, with IBB up 24% and XBI up 28%, driven by therapeutic breakthroughs and M&A. Panelists expect continued M&A and AI-driven drug discovery, while noting tech sector rotation risks. Upcoming trial readouts include Librexia-AF and Summit's HARMONi-3.Ophthalmology TimesHigh-resolution multimodal imaging is key in dry AMD therapeutic development, future managementInvestigators are exploring multiple strategies to combat dry age-related macular degeneration (AMD), particularly using high-resolution optical coherence tomography (OCT) for monitoring disease progression. Notable compounds in development include pegcetacoplan from Apellis Pharmaceuticals and Zimura from Iveric Bio, with promising results in clinical trials noted for therapies targeting inflammation and oxidative stress. The advancements in OCT technology enhance the ability to track treatment efficacy and disease markers, underscoring the importance of these innovations in future management.Ophthalmology TimesBeth Marsh appointed as new Neurotech chief commercial officerNeurotech Pharmaceuticals has appointed Beth Marsh as its new chief commercial officer to lead the US launch of ENCELTO, a treatment for idiopathic macular telangiectasia type 2. Marsh brings over two decades of ophthalmology leadership experience, having previously managed commercial launches at Apellis Pharmaceuticals and held roles at Shire/Takeda. The appointment aligns with the FDA's March approval of ENCELTO, marking it as the first approved therapy for this condition.The Motley FoolWhy Biogen Stock Topped the Market TodayBiogen reported Q2 revenue of $2.7 billion, up 3% year-over-year, and adjusted EPS of $3.60, down from $5.30. The stock rose nearly 2% on the day, outpacing the S&P 500. The company lowered its full-year adjusted EPS guidance to $12–$13 per share.Markets DailyBiogen (NASDAQ:BIIB) Issues Quarterly Earnings ResultsBiogen reported second-quarter earnings with adjusted EPS of $3.60, beating the consensus estimate of $2.94, while revenue of $2.74 billion exceeded expectations of $2.46 billion and rose 3.4% year over year. The company raised its 2026 revenue outlook from a mid-single-digit decline to a mid-single-digit increase and now expects non-GAAP EPS of $12 to $13, driven by 24% growth in its growth portfolio which surpassed the legacy multiple sclerosis portfolio. The Apellis acquisition, completed on May 14, contributed $128 million in SYFOVRE and EMPAVELI revenue, while Biogen expects at least $250 million in annual run-rate synergies by the end of 2027.pharmaphorumLeqembi sales grow again after subcutaneous approvalsBiogen's Q2 results show Leqembi sales rose 15% to $184 million, with $97 million from the US. The growth follows approvals of a subcutaneous version, which Biogen expects to push annual sales above $1 billion. The company also reported gains in other franchises, including Zurzuvae and Empaveli.Ophthalmology TimesASRS 2026: AI-matched analysis finds pegcetacoplan slows visual acuity decline in GAA retrospective analysis using the Vestrum database presented at ASRS 2026 found that geographic atrophy patients treated with pegcetacoplan (Syfovre, Apellis Pharmaceuticals) were more likely to maintain visual acuity or show slower decline compared to untreated patients, with statistically significant differences at 6, 12, and 18 months in patients losing 15 letters or more. The AI-assisted matching study included both GA-alone patients and GA patients with concurrent neovascular AMD, with the visual acuity benefit most pronounced in the combination-therapy cohort. Researchers noted this represents the first demonstration of a visual acuity benefit with pegcetacoplan treatment and suggested the findings support expanded use in combination with anti-VEGF therapy, with patients requiring less frequent anti-VEGF dosing due to the more atrophic disease phase.DevdiscourseGlobal Health Updates: Ebola Efforts and Pharmaceutical DevelopmentsBiogen is scaling back Apellis Pharmaceuticals' research programs and cutting jobs following its $5.6 billion acquisition, while focusing on integrating the Empaveli and Syfovre therapies. The U.S. Department of Health is combating an Ebola Bundibugyo outbreak in Africa by deploying vaccines and experimental treatments in the Democratic Republic of the Congo and Uganda. Additionally, the FDA proposed a regulatory rule to control illegal foreign tobacco imports to address youth e-cigarette use.DevdiscourseGlobal Health Headlines: Ebola, Pharmaceuticals, and Drug RegulationsBiogen announced it is pulling back research funding for Apellis Pharmaceuticals after acquiring the firm for $5.6 billion. The U.S. Department of Health and Human Services is working on developing an Ebola vaccine amid outbreaks in the Democratic Republic of the Congo and Uganda. Additionally, the FDA proposed regulations to control illegal tobacco imports, especially e-cigarettes favored by youth.PR NewswireSobi to present new data on pegcetacoplan at ERA 2026Sobi announced that new data from the pegcetacoplan clinical development programme will be presented at the 63rd Congress of the European Renal Association (ERA) in Glasgow, UK from 3-6 June 2026. The presentations include analyses from the pivotal Phase 3 VALIANT study and its long-term extension VALE study evaluating pegcetacoplan in patients with C3 glomerulopathy and primary immune-complex membranoproliferative glomerulonephritis, covering treatment response, safety, and tolerability data. The studies are being conducted in collaboration with Apellis Pharmaceuticals, now part of Biogen, with Sobi holding exclusive ex-U.S. commercialization rights and Apellis holding U.S. commercialization rights for systemic pegcetacoplan.