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Star Therapeutics

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uuid00000sj

Namestring
Star Therapeutics
Legal namestring
Star OpCo, Inc.
Company typeenum
Private
Founded yearint
2018
Descriptiontext

Star Therapeutics is a late clinical-stage biotechnology company founded in 2018 and headquartered in South San Francisco that operates a hub-and-spoke model in which a central R&D engine generates first-in-class antibody therapies, each housed in a dedicated subsidiary focused on a specific area of biology. Its lead program, VGA039 (under the Vega Therapeutics subsidiary), is a first-in-class fully human IgG4 monoclonal antibody that targets Protein S to restore hemostasis via dual mechanisms — promoting platelet attachment and enhancing fibrin deposition — and is being advanced as a once-monthly subcutaneous prophylactic therapy for von Willebrand disease (VWD), currently in pivotal Phase 3 (VIVID-6). A second subsidiary, Electra Therapeutics, develops antibody therapies for rare inflammatory diseases, with lead candidate ELA026 in Phase II/III for secondary hemophagocytic lymphohistiocytosis (sHLH) and a second candidate ELA822 entering the clinic.

The company's technology platform emphasizes a pipeline-in-a-product strategy, in which each antibody is designed to address multiple diseases from a single biological target, supported by a leadership team that has previously invented four first-in-class antibodies, including ENJAYMO (the first approved drug for cold agglutinin disease). VGA039 has accumulated four FDA designations (Fast Track, Orphan Drug, Rare Pediatric Disease, and Breakthrough Therapy) and has demonstrated 73-100% reductions in annualized bleeding rates in interim Phase 1/2 data with nearly 100% subcutaneous bioavailability and a 25-day half-life.

Star is privately held and pre-revenue, with no products on market. Capital formation has been the primary financing mechanism: more than $300M has been raised across multiple rounds led by top-tier life sciences investors (Sofinnova, Sanofi Ventures, Viking Global, OrbiMed, RA Capital, Westlake Village BioPartners). The company's near-term value realization is anchored by Incyte's June 2026 definitive agreement to acquire Vega Therapeutics for $1.25B upfront plus up to $750M in sales milestones, expected to close in Q3 2026. The intended commercial model upon approval is a specialty-pharmacy-driven, hematology-focused launch targeting the approximately 135,000 diagnosed VWD patients in the U.S.

Short descriptiontext

Star Therapeutics is a South San Francisco-based clinical-stage biotechnology company founded in 2018 that discovers first-in-class antibody therapies for rare diseases through a hub-and-spoke subsidiary model, with lead asset VGA039 in Phase 3 for von Willebrand disease. The company is pre-revenue and pending the $2B Incyte acquisition of its Vega subsidiary.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersSouth San Francisco, United States
HQ citystring
South San Francisco
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
antibody therapeutics, monoclonal antibody therapy, bleeding disorder treatments, biopharmaceutical drug discovery, rare disease therapies
Industry2 codes
PRIMARYHLAAAAAA
Monoclonal Antibody Therapeutics (mAbs)
Healthcare & Life Sciences/Biotechnology & Biologics/Therapeutic Biologics (mAbs, recombinant proteins, cytokines)
SECONDARYHLAAAIAB
Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering)
Healthcare & Life Sciences/Biotechnology & Biologics/Biologic Drug Discovery Platforms (screening, antibody engineering, synthetic biology)
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Biopharmaceuticals
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Pharmaceutical Product Sales
TypeOne Time License
Description

Star Therapeutics is a late clinical-stage biotech company with products in Phase 3 development. Revenue will be generated through commercial sales of approved biologic therapeutics, initially VGA039 for von Willebrand disease if approved. The company has been acquired by Incyte for its Vega Therapeutics subsidiary containing VGA039, indicating a future exit pathway.

fiercebiotech.com
2Subsidiary Exits/Acquisitions
TypeLicensing Royalties
Description

Star Therapeutics operates with a hub-and-spoke model, spinning out subsidiaries focused on specific therapeutic areas. The company has demonstrated success with exits, including contributions to True North Therapeutics acquisition by Bioverativ ($825M) and iPierian acquisition by BMS ($725M). Incyte's acquisition of Vega Therapeutics for up to $2B represents a major exit.

fiercebiotech.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1Electra Therapeutics
Description

Subsidiary company focused on rare inflammatory diseases with lead drug candidate ELA026 for secondary hemophagocytic lymphohistiocytosis (sHLH).

star-therapeutics.com
+1 more record
Core offering1 text field

Star Therapeutics is a late clinical-stage biotechnology company that discovers and develops first-in-class antibody therapeutics for rare diseases. Its lead program, VGA039, is a monoclonal antibody targeting Protein S currently in Phase 3 development as a once-monthly subcutaneous prophylactic therapy for von Willebrand disease (VWD). The company operates a hub-and-spoke model, with wholly owned subsidiaries (Vega Therapeutics for bleeding disorders, Electra Therapeutics for inflammatory diseases) developing additional antibody candidates such as ELA026 and ELA822.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • 73-87% reduction in annualized bleeding rate (ABR) for patients with ABR ≥ 12, no prior IV prophylaxis
+4 more records
Product overview1 text field

Star Therapeutics is a late clinical-stage biotechnology company that operates as an innovation engine with a hub-and-spoke model, creating subsidiary companies focused on specific areas of biology. The company's lead product is VGA039 (under the VEGA Program brand), a first-in-class monoclonal antibody targeting Protein S for the treatment of bleeding disorders, starting with von Willebrand disease (VWD). The company also has subsidiary Electra Therapeutics developing therapies (ELA026, ELA822) for rare inflammatory diseases. Star Therapeutics' pipeline includes multiple first-in-class antibody therapeutics, with one approved drug (ENJAYMO for cold agglutinin disease) and others in Phase 3 development. Based in South San Francisco, the company has raised more than $300 million from leading life sciences investors.

Product and service3 records
1VGA039
CategoryMonoclonal Antibody Therapeutic (Investigational Biologic)
Description

VGA039 is a first-in-class fully human IgG4 monoclonal antibody that targets Protein S to restore hemostasis, with dual actions promoting platelet attachment and enhancing fibrin deposition. It is being developed as a once-monthly subcutaneous prophylactic therapy for von Willebrand disease (VWD) and potentially other bleeding disorders, and is currently in Phase 3 development (VIVID-6 trial) with FDA Fast Track, Orphan Drug, Rare Pediatric Disease, and Breakthrough Therapy designations.

2ELA026
CategoryMonoclonal Antibody Therapeutic (Investigational Biologic)
Description

ELA026 is an investigational antibody drug candidate developed by Star Therapeutics' wholly owned subsidiary Electra Therapeutics for the treatment of secondary hemophagocytic lymphohistiocytosis (sHLH), a rare hyperinflammatory condition. It is in Phase II/III clinical development with regulatory designations supporting its advancement.

3ELA822
CategoryMonoclonal Antibody Therapeutic (Investigational Biologic)
Description

ELA822 is a second antibody drug candidate developed by Star Therapeutics' subsidiary Electra Therapeutics that is being advanced into clinical trials for an undisclosed rare inflammatory disease indication, funded by Electra's Series C financing.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierFlagshipTypeStrategic or Co-development Partner
Description

Incyte announced acquisition of Vega Therapeutics (wholly owned subsidiary of Star) for $1.25 billion upfront plus up to $750 million in sales milestones (total up to $2 billion). Deal expected to close Q3 2026 pending regulatory approval. VGA039 will be added to Incyte's hematology portfolio.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Patient advocacy organization partnership for VWD awareness and patient education. Executive Director Jeanette Cesta has publicly supported VGA039 development.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

First subsidiary of Star Therapeutics, focused on rare inflammatory diseases. Electra completed $183 million Series C financing for ELA026 in secondary hemophagocytic lymphohistiocytosis (sHLH). Adam Rosenthal remains Board Director.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers8 records
TypeDirect peer
Description

Argenx is a late-stage immunology biotech developing first-in-class antibody therapeutics (efgartigimod/VYVGART franchise), with a similar antibody-discovery-platform model and focus on rare autoimmune diseases. Comparable in clinical-stage maturity, mAb modality, and rare-disease commercial strategy.

TypeBroad incumbent
Description

BioMarin is an established rare-disease biotech with a commercial rare-hematology and specialty biologics portfolio. Overlaps with Star in rare genetic/bleeding disorder focus and biologic modality, though BioMarin operates at a much larger commercial scale.

TypeDirect peer
Description

Sobi is a global rare-disease company with a dedicated hemophilia and bleeding-disorder franchise (Eloctate, Alprolix). Directly comparable to Star in therapeutic focus (VWD/hemophilia) and biologics commercialization, though Sobi operates as a commercial-stage incumbent.

TypeDirect peer
Description

BridgeBio operates a hub-and-spoke model of subsidiary biotech companies focused on rare genetic diseases, mirroring Star's constellation structure. Comparable in capital structure, late-stage clinical assets, and subsidiary-driven value creation, though BridgeBio has broader therapeutic diversification.

TypeBroad incumbent
Description

Alexion (acquired by AstraZeneca) is a commercial rare-disease antibody franchise with a focus on complement-mediated and hematologic rare diseases (Soliris, Ultomiris, Strensiq). Closely comparable therapeutic area (rare hematology) and monoclonal antibody modality at commercial scale.

TypeDirect peer
Description

Genmab is a leading antibody discovery and engineering platform company that invents and develops differentiated mAb therapeutics through proprietary technology. Closely comparable to Star's antibody discovery engine and pipeline-in-a-product strategy, though Genmab operates a partnership/licensing model at scale.

TypeBroad incumbent
Description

Alnylam is a commercial-stage rare-disease biotech developing RNA interference therapeutics for hematologic and other rare disorders. Comparable in late-stage clinical maturity, rare-disease focus, and orphan-drug commercial strategy, with overlapping treatment-center channels.

TypeBroad incumbent
Description

Takeda acquired Shire and operates an established hemophilia and rare-bleeding-disorder commercial franchise (Adynovate, Rixubis). Directly competitive in the bleeding-disorder treatment center channel and comparable in target patient population, though Takeda operates at significantly larger commercial scale.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

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

Segment2 records

Each record includes

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

Ideal customer profile2 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
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles7 records

Each record includes

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

Subsidiaries2 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds3 records

Each record includes

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

Investors19 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&A

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 →

Star Therapeutics

Biopharmaceuticalsstar-therapeutics.com

Star Therapeutics is a South San Francisco-based clinical-stage biotechnology company founded in 2018 that discovers first-in-class antibody therapies for rare diseases through a hub-and-spoke subsidiary model, with lead asset VGA039 in Phase 3 for von Willebrand disease. The company is pre-revenue and pending the $2B Incyte acquisition of its Vega subsidiary.

What Star Therapeutics does

Star Therapeutics is a late clinical-stage biotechnology company founded in 2018 and headquartered in South San Francisco that operates a hub-and-spoke model in which a central R&D engine generates first-in-class antibody therapies, each housed in a dedicated subsidiary focused on a specific area of biology. Its lead program, VGA039 (under the Vega Therapeutics subsidiary), is a first-in-class fully human IgG4 monoclonal antibody that targets Protein S to restore hemostasis via dual mechanisms — promoting platelet attachment and enhancing fibrin deposition — and is being advanced as a once-monthly subcutaneous prophylactic therapy for von Willebrand disease (VWD), currently in pivotal Phase 3 (VIVID-6). A second subsidiary, Electra Therapeutics, develops antibody therapies for rare inflammatory diseases, with lead candidate ELA026 in Phase II/III for secondary hemophagocytic lymphohistiocytosis (sHLH) and a second candidate ELA822 entering the clinic.

The company's technology platform emphasizes a pipeline-in-a-product strategy, in which each antibody is designed to address multiple diseases from a single biological target, supported by a leadership team that has previously invented four first-in-class antibodies, including ENJAYMO (the first approved drug for cold agglutinin disease). VGA039 has accumulated four FDA designations (Fast Track, Orphan Drug, Rare Pediatric Disease, and Breakthrough Therapy) and has demonstrated 73-100% reductions in annualized bleeding rates in interim Phase 1/2 data with nearly 100% subcutaneous bioavailability and a 25-day half-life.

Star is privately held and pre-revenue, with no products on market. Capital formation has been the primary financing mechanism: more than $300M has been raised across multiple rounds led by top-tier life sciences investors (Sofinnova, Sanofi Ventures, Viking Global, OrbiMed, RA Capital, Westlake Village BioPartners). The company's near-term value realization is anchored by Incyte's June 2026 definitive agreement to acquire Vega Therapeutics for $1.25B upfront plus up to $750M in sales milestones, expected to close in Q3 2026. The intended commercial model upon approval is a specialty-pharmacy-driven, hematology-focused launch targeting the approximately 135,000 diagnosed VWD patients in the U.S.

Star Therapeutics firmographics

Firmographics
Name
Star Therapeutics
Legal name
Star OpCo, Inc.
Website
https://star-therapeutics.com
Company type
Private
Founded year
2018
Operating status
Operating
Headcount range
11–50 employees
Short description
Star Therapeutics is a South San Francisco-based clinical-stage biotechnology company founded in 2018 that discovers first-in-class antibody therapies for rare diseases through a hub-and-spoke subsidiary model, with lead asset VGA039 in Phase 3 for von Willebrand disease. The company is pre-revenue and pending the $2B Incyte acquisition of its Vega subsidiary.
Ownership category
akta.pro rank

Star Therapeutics industry classification

Industry
Product category
Biopharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro industry
PRIMARYHLAAAAAA
Monoclonal Antibody Therapeutics (mAbs)
Healthcare & Life Sciences/Biotechnology & Biologics/Therapeutic Biologics (mAbs, recombinant proteins, cytokines)
SECONDARYHLAAAIAB
Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering)
Healthcare & Life Sciences/Biotechnology & Biologics/Biologic Drug Discovery Platforms (screening, antibody engineering, synthetic biology)

Keywords

  • Antibody therapeutics
  • Monoclonal antibody therapy
  • Bleeding disorder treatments
  • Biopharmaceutical drug discovery
  • Rare disease therapies

Where Star Therapeutics is headquartered

Location

Headquarters

HQ city
South San Francisco
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Star Therapeutics business model

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

Revenue model

  1. Pharmaceutical Product Sales: Star Therapeutics is a late clinical-stage biotech company with products in Phase 3 development. Revenue will be generated through commercial sales of approved biologic therapeutics, initially VGA039 for von Willebrand disease if approved. The company has been acquired by Incyte for its Vega Therapeutics subsidiary containing VGA039, indicating a future exit pathway.
  2. Subsidiary Exits/Acquisitions: Star Therapeutics operates with a hub-and-spoke model, spinning out subsidiaries focused on specific therapeutic areas. The company has demonstrated success with exits, including contributions to True North Therapeutics acquisition by Bioverativ ($825M) and iPierian acquisition by BMS ($725M). Incyte's acquisition of Vega Therapeutics for up to $2B represents a major exit.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels5 records

Star Therapeutics product offering

Product offering

Core offering

Star Therapeutics is a late clinical-stage biotechnology company that discovers and develops first-in-class antibody therapeutics for rare diseases. Its lead program, VGA039, is a monoclonal antibody targeting Protein S currently in Phase 3 development as a once-monthly subcutaneous prophylactic therapy for von Willebrand disease (VWD). The company operates a hub-and-spoke model, with wholly owned subsidiaries (Vega Therapeutics for bleeding disorders, Electra Therapeutics for inflammatory diseases) developing additional antibody candidates such as ELA026 and ELA822.

Product overview

Star Therapeutics is a late clinical-stage biotechnology company that operates as an innovation engine with a hub-and-spoke model, creating subsidiary companies focused on specific areas of biology. The company's lead product is VGA039 (under the VEGA Program brand), a first-in-class monoclonal antibody targeting Protein S for the treatment of bleeding disorders, starting with von Willebrand disease (VWD). The company also has subsidiary Electra Therapeutics developing therapies (ELA026, ELA822) for rare inflammatory diseases. Star Therapeutics' pipeline includes multiple first-in-class antibody therapeutics, with one approved drug (ENJAYMO for cold agglutinin disease) and others in Phase 3 development. Based in South San Francisco, the company has raised more than $300 million from leading life sciences investors.

Differentiator

Problem solved

Functional benefit

Brands

  • Electra Therapeutics: Subsidiary company focused on rare inflammatory diseases with lead drug candidate ELA026 for secondary hemophagocytic lymphohistiocytosis (sHLH).
  • Vega Therapeutics

Products and services

  • VGA039 VGA039 is a first-in-class fully human IgG4 monoclonal antibody that targets Protein S to restore hemostasis, with dual actions promoting platelet attachment and enhancing fibrin deposition. It is being developed as a once-monthly subcutaneous prophylactic therapy for von Willebrand disease (VWD) and potentially other bleeding disorders, and is currently in Phase 3 development (VIVID-6 trial) with FDA Fast Track, Orphan Drug, Rare Pediatric Disease, and Breakthrough Therapy designations.
  • ELA026 ELA026 is an investigational antibody drug candidate developed by Star Therapeutics' wholly owned subsidiary Electra Therapeutics for the treatment of secondary hemophagocytic lymphohistiocytosis (sHLH), a rare hyperinflammatory condition. It is in Phase II/III clinical development with regulatory designations supporting its advancement.
  • ELA822 ELA822 is a second antibody drug candidate developed by Star Therapeutics' subsidiary Electra Therapeutics that is being advanced into clinical trials for an undisclosed rare inflammatory disease indication, funded by Electra's Series C financing.

Quantifiable outcome

  • 73-87% reduction in annualized bleeding rate (ABR) for patients with ABR ≥ 12, no prior IV prophylaxis
  • +4 more outcomes

Companies that use Star Therapeutics

Customer profile

Named customers1 record

Segments2 records

Ideal customer profiles2 records

Star Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Star Therapeutics partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered flagship, minor and core.

  • Incyte CorporationflagshipStrategic or Co-development PartnerIncyte announced acquisition of Vega Therapeutics (wholly owned subsidiary of Star) for $1.25 billion upfront plus up to $750 million in sales milestones (total up to $2 billion). Deal expected to close Q3 2026 pending regulatory approval. VGA039 will be added to Incyte's hematology portfolio.
  • VWD Connect FoundationminorStrategic or Co-development PartnerPatient advocacy organization partnership for VWD awareness and patient education. Executive Director Jeanette Cesta has publicly supported VGA039 development.
  • Electra TherapeuticscoreStrategic or Co-development PartnerFirst subsidiary of Star Therapeutics, focused on rare inflammatory diseases. Electra completed $183 million Series C financing for ELA026 in secondary hemophagocytic lymphohistiocytosis (sHLH). Adam Rosenthal remains Board Director.

Scale indicators6 records

Recent moves8 records

Expansion highlights6 records

Star Therapeutics competitors and assessment

Company assessment

Direct peers

  • Argenx: Argenx is a late-stage immunology biotech developing first-in-class antibody therapeutics (efgartigimod/VYVGART franchise), with a similar antibody-discovery-platform model and focus on rare autoimmune diseases. Comparable in clinical-stage maturity, mAb modality, and rare-disease commercial strategy.
  • Swedish Orphan Biovitrum (Sobi): Sobi is a global rare-disease company with a dedicated hemophilia and bleeding-disorder franchise (Eloctate, Alprolix). Directly comparable to Star in therapeutic focus (VWD/hemophilia) and biologics commercialization, though Sobi operates as a commercial-stage incumbent.
  • BridgeBio Pharma: BridgeBio operates a hub-and-spoke model of subsidiary biotech companies focused on rare genetic diseases, mirroring Star's constellation structure. Comparable in capital structure, late-stage clinical assets, and subsidiary-driven value creation, though BridgeBio has broader therapeutic diversification.
  • Genmab: Genmab is a leading antibody discovery and engineering platform company that invents and develops differentiated mAb therapeutics through proprietary technology. Closely comparable to Star's antibody discovery engine and pipeline-in-a-product strategy, though Genmab operates a partnership/licensing model at scale.

Broad incumbents

  • BioMarin Pharmaceutical: BioMarin is an established rare-disease biotech with a commercial rare-hematology and specialty biologics portfolio. Overlaps with Star in rare genetic/bleeding disorder focus and biologic modality, though BioMarin operates at a much larger commercial scale.
  • Alexion / AstraZeneca Rare Disease: Alexion (acquired by AstraZeneca) is a commercial rare-disease antibody franchise with a focus on complement-mediated and hematologic rare diseases (Soliris, Ultomiris, Strensiq). Closely comparable therapeutic area (rare hematology) and monoclonal antibody modality at commercial scale.
  • Alnylam Pharmaceuticals: Alnylam is a commercial-stage rare-disease biotech developing RNA interference therapeutics for hematologic and other rare disorders. Comparable in late-stage clinical maturity, rare-disease focus, and orphan-drug commercial strategy, with overlapping treatment-center channels.
  • Takeda Pharmaceutical (Rare Bleeding Franchise): Takeda acquired Shire and operates an established hemophilia and rare-bleeding-disorder commercial franchise (Adynovate, Rixubis). Directly competitive in the bleeding-disorder treatment center channel and comparable in target patient population, though Takeda operates at significantly larger commercial scale.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Star Therapeutics social profiles

Digital presence

Star Therapeutics financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Star Therapeutics leadership team

Management profile

Number of profiles

Profiles7 records

Star Therapeutics subsidiaries and ownership

Company hierarchy

Subsidiaries2 records

Star Therapeutics funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors19 records

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

Star Therapeutics M&A and investment

M&A and investment

M&A

Investments

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

Frequently asked questions about Star Therapeutics

What does Star Therapeutics do?

Star Therapeutics is a late clinical-stage biotechnology company that discovers and develops first-in-class antibody therapeutics for rare diseases. Its lead program, VGA039, is a monoclonal antibody targeting Protein S currently in Phase 3 development as a once-monthly subcutaneous prophylactic therapy for von Willebrand disease (VWD). The company operates a hub-and-spoke model, with wholly owned subsidiaries (Vega Therapeutics for bleeding disorders, Electra Therapeutics for inflammatory diseases) developing additional antibody candidates such as ELA026 and ELA822.

Is Star Therapeutics a public or private company?

Star Therapeutics is a private company. It is classified as venture growth investor backed and is currently operating.

When was Star Therapeutics founded?

Star Therapeutics was founded in 2018. It employs 11 to 50 people.

Where is Star Therapeutics based?

Star Therapeutics is headquartered in South San Francisco, United States, in the North America region.

How does Star Therapeutics make money?

Two revenue lines are on record. Pharmaceutical Product Sales are the primary driver. The others are subsidiary Exits/Acquisitions.

Who are Star Therapeutics's main competitors?

Direct peers on record are Argenx, Swedish Orphan Biovitrum (Sobi), BridgeBio Pharma and Genmab. Broad incumbents are BioMarin Pharmaceutical, Alexion / AstraZeneca Rare Disease, Alnylam Pharmaceuticals and Takeda Pharmaceutical (Rare Bleeding Franchise).

Does Star Therapeutics have an API?

No public API is recorded for Star Therapeutics.

What industry is Star Therapeutics in?

Star Therapeutics's product category is Biopharmaceuticals. Its primary akta.pro industry code is HLAAAAAA, Monoclonal Antibody Therapeutics (mAbs), with a secondary code of HLAAAIAB, Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering). Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
FinancialContent Business PageIncyte Completes Acquisition of Vega Therapeutics, a Wholly Owned Subsidiary of Star Therapeutics, Expanding its Hematology PortfolioIncyte announced the completion of its acquisition of Vega Therapeutics, a wholly owned subsidiary of Star Therapeutics, for $1.25 billion upfront with up to $750 million in additional sales milestone payments. The deal adds VGA039, a novel monoclonal antibody in Phase 3 development for von Willebrand disease, to Incyte's hematology portfolio; VGA039 has received FDA Breakthrough Therapy, Fast Track, Orphan Drug, and Rare Pediatric Disease designations and is being evaluated in the global Phase 3 VIVID-6 study. The transaction is expected to be recorded as a one-time R&D expense in the third quarter and full year 2026 GAAP and non-GAAP financial results.Business Wire BlogIncyte Completes Acquisition of Vega Therapeutics, a Wholly Owned Subsidiary of Star Therapeutics, Expanding its Hematology PortfolioIncyte has completed its acquisition of Vega Therapeutics, Inc., a wholly owned subsidiary of Star Therapeutics LLC, for $1.25 billion upfront plus up to $750 million in sales milestone payments. The deal adds VGA039, a novel monoclonal antibody in Phase 3 development for von Willebrand disease (VWD), to Incyte's hematology portfolio, with VGA039 carrying FDA Breakthrough Therapy, Fast Track, orphan drug and rare pediatric disease designations. VGA039 has the potential to become the first once-monthly subcutaneous prophylactic therapy for VWD patients, who currently require frequent intravenous infusions.Stock TitanIncyte closes Vega buy, adds Phase 3 VGA039Incyte has completed its acquisition of Vega Therapeutics, Inc., a wholly owned subsidiary of Star Therapeutics LLC, for $1.25 billion upfront with up to $750 million in additional sales milestone payments. The deal adds VGA039, a novel investigational monoclonal antibody in Phase 3 development for von Willebrand disease (VWD), to Incyte's hematology portfolio, with VGA039 having received Breakthrough Therapy, Fast Track, Orphan drug and rare pediatric disease designations from the FDA. If approved, VGA039 has the potential to become the first once-monthly subcutaneous prophylactic therapy for VWD patients, who currently require frequent intravenous infusions.citybizIncyte Completes $1.25 Billion Vega Therapeutics Acquisition, Adding Late-Stage Bleeding Disorder TherapyIncyte completed its $1.25 billion acquisition of Vega Therapeutics, adding VGA039, a Phase 3 therapy for von Willebrand disease. The deal includes up to $750 million in milestone payments, and Incyte expects to record the acquisition as a one-time R&D expense in Q3 and full-year 2026 results.IncyteIncyte Completes Acquisition of Vega Therapeutics, a Wholly Owned Subsidiary of Star Therapeutics, Expanding its Hematology PortfolioIncyte completed its acquisition of Vega Therapeutics, a wholly owned subsidiary of Star Therapeutics, adding VGA039 to its hematology portfolio. VGA039 is a Phase 3 monoclonal antibody for von Willebrand disease, with potential as a first-in-class once-monthly subcutaneous prophylactic therapy. The acquisition expands Incyte's presence in bleeding disorders.BioSpaceStar Therapeutics to Present Complete Data from Phase 1/2 Multidose Study of VGA039 in Von Willebrand Disease at ISTH 2026 CongressStar Therapeutics will present complete Phase 1/2 data on its VGA039 antibody for von Willebrand disease at ISTH 2026 in Paris. The company also announced Incyte's $1.25 billion acquisition of its subsidiary Vega Therapeutics, with up to $750 million in milestone payments. VGA039 is in Phase 3 development as a potential once-monthly subcutaneous prophylaxis.Investing.comStar Therapeutics to present VGA039 data at ISTH congress By Investing.comStar Therapeutics announced it will present safety and efficacy data from its Phase 1/2 multidose study of VGA039 for von Willebrand disease at the 34th Congress of the International Society on Thrombosis and Haemostasis in Paris, July 2026. Earlier this month, Incyte announced a definitive agreement to acquire Vega Therapeutics, a wholly owned subsidiary of Star Therapeutics, for $1.25 billion upfront with potential additional payments up to $750 million, bringing total consideration to $2.0 billion. The acquisition has driven Incyte shares near their 52-week high, with analysts offering mixed outlooks following a separate $246 million Medicaid settlement benefit.Business Wire BlogStar Therapeutics to Present Complete Data from Phase 1/2 Multidose Study of VGA039 in Von Willebrand Disease at ISTH 2026 CongressStar Therapeutics announced it will present complete safety and efficacy data from its Phase 1/2 multidose study of VGA039 for von Willebrand disease at the ISTH 2026 Congress in Paris, July 11-15, 2026, including oral presentations and poster sessions on the novel monoclonal antibody therapy. Incyte recently entered into a definitive agreement to acquire Vega Therapeutics, Inc., a wholly owned subsidiary of Star Therapeutics, for $1.25 billion upfront with potential additional payments up to $2.0 billion total. VGA039, a Protein S-targeting antibody in Phase 3 development, has received Fast Track, Orphan Drug, Rare Pediatric Disease, and Breakthrough Therapy designations from the FDA and has potential to be the first subcutaneous prophylactic therapy for all types of VWD with once-monthly dosing.Stock TitanStar Therapeutics to present VGA039 Phase 1/2 dataStar Therapeutics announced it will present complete safety and efficacy data from its Phase 1/2 multidose study of VGA039 for von Willebrand disease at the ISTH 2026 Congress in Paris, France (July 11-15). VGA039 is an investigational monoclonal antibody therapy in Phase 3 development with potential to be the first subcutaneous prophylactic treatment for all types of VWD with once-monthly dosing. Earlier this month, Incyte entered into a definitive agreement to acquire Vega Therapeutics (a Star Therapeutics subsidiary) for $1.25 billion upfront, with up to $750 million in additional milestone payments, totaling up to $2.0 billion.FinancialContent Business PageStar Therapeutics to Present Complete Data from Phase 1/2 Multidose Study of VGA039 in Von Willebrand Disease at ISTH 2026 CongressStar Therapeutics announced it will present complete safety and efficacy data from its Phase 1/2 multidose study of VGA039 for von Willebrand disease at the ISTH 2026 Congress in Paris, with the investigational therapy now in Phase 3 development as a potential first subcutaneous prophylactic treatment for all VWD types with once-monthly dosing. Earlier this month, Incyte entered into a definitive agreement to acquire Vega Therapeutics, Inc. (a wholly owned subsidiary of Star Therapeutics) for $1.25 billion upfront plus up to $750 million in sales milestones, totaling up to $2.0 billion in potential consideration. VGA039 has received Fast Track, orphan drug, rare pediatric disease and Breakthrough Therapy designations from the FDA and is advancing through a global Phase 3 study.