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Abbisko Therapeutics

Full company profile

uuid0000z7r

Namestring
Abbisko Therapeutics
Legal namestring
Abbisko Therapeutics Co., Ltd.
Websiteurl
abbisko.com
Company typeenum
Public
Founded yearint
2016
Descriptiontext

Abbisko Therapeutics is a Shanghai-based, HKEX-listed (02256.HK) clinical-stage biopharmaceutical company founded in 2016 by pharma veterans including Dr. Yao-Chang Xu (former Eli Lilly) and Dr. Hongping Yu. The company focuses on discovering and developing differentiated small-molecule therapies for precision oncology, immuno-oncology, and rare diseases, with a pipeline of 11+ candidates spanning FGFR (ABSK011/irpagratinib, ABSK091/fexagratinib, ABSK061, ABSK121, ABSK012), CSF-1R (ABSK021/pimicotinib), EGFR (ABSK112, ABK3376), CXCR4 (mavorixafor/ABSK081), oral PD-L1 (ABSK043), CD73 (ABSK051), PRMT5 (ABSK131), and preclinical KRAS G12D and pan-KRAS programs. The business model is asset-light and partnership-driven: Abbisko retains Greater China rights for key assets while out-licensing regional and global ex-China development and commercialization to top-tier pharma partners (Eli Lilly, Merck KGaA, AstraZeneca, Roche, BeiGene, X4 Pharmaceuticals, Aileisi), generating revenue through upfront payments, development/regulatory/commercial milestones, and tiered royalties on net sales. The company achieved its first regulatory approval in December 2025 with China NMPA's approval of pimicotinib for tenosynovial giant cell tumor, followed by FDA NDA acceptance in January 2026; a 2026 expansion of the Eli Lilly collaboration represents up to $1.9 billion in potential milestones, signaling a transition from clinical development to early commercialization across China, the US, and Europe.

Short descriptiontext

Abbisko Therapeutics is a Shanghai-based, HKEX-listed clinical-stage biopharmaceutical company that discovers and develops differentiated small-molecule therapies for precision oncology, immuno-oncology, and rare diseases, out-licensing regional and global rights to top-tier pharma partners while retaining Greater China rights.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersShanghai, China
HQ citystring
Shanghai
HQ countrystring
China
HQ regionstring
Asia
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
precision oncology drugs, small molecule therapeutics, targeted cancer therapy, FGFR inhibitors, immuno-oncology drugs
Industry4 codes
1Oncology & Hematology Pharmaceuticals
CodeHLAIAAACPrimaryYes
2Rare Oncology & Hematologic Malignancy Therapies
CodeHLAIAIACPrimaryNo
3Oncology Specialty Pharmaceuticals
CodeHLAIACAAPrimaryNo
4Specialty Care Pharmaceuticals
CodeHLAIAAABPrimaryNo
NAICS code3 codes
  • Pharmaceutical and Medicine Manufacturing3254
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Pharmaceutical Preparation Manufacturing325412
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Medicinal Chemicals & Botanical Products2833
Product category
Precision Oncology Pharmaceuticals
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Licensing and Milestone Payments
TypeLicensing Royalties
Description

Abbisko generates revenue through licensing deals in which it grants regional or global rights to its pipeline assets in exchange for upfront payments, development and regulatory milestone payments, and commercial milestone payments. The 2022 Eli Lilly collaboration and its 2026 $1.9 billion expansion represent the flagship example. Milestone payments are triggered upon achievement of clinical, regulatory, and commercial milestones.

2Royalties on Net Sales
TypeLicensing Royalties
Description

Following regulatory approval and commercialization of licensed assets, Abbisko receives royalty payments on net sales from its commercialization partners. Royalties provide recurring revenue tied to commercial performance of approved therapies in partnered territories.

Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels7 records

Each record includes

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

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Supply Chain
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1贝捷迈® (Pimicotinib)
Description

Brand name for Pimicotinib (ABSK021), the company's CSF-1R inhibitor approved in China for tenosynovial giant cell tumor.

abbisko.com
Core offering1 text field

Abbisko Therapeutics discovers and develops differentiated small-molecule therapies for cancer and rare diseases, with a pipeline of 15+ clinical-stage and preclinical programs targeting FGFR, CSF-1R, KRAS, EGFR, PD-L1, CD73, and other oncology mechanisms. The company pursues a partnership-driven commercialization model, out-licensing global or regional rights to major pharmaceutical partners while retaining rights in Greater China for select assets.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 2 values shown
  • Potential deal value of up to $1.9 billion in the expanded Eli Lilly partnership for pimicotinib and another asset (2026)
+1 more record
Product overview1 text field

Abbisko Therapeutics is a Shanghai-based clinical-stage biopharmaceutical company founded in 2016, focused on discovering and developing novel and differentiated small-molecule therapies for cancer and beyond. The company's in-house R&D engine encompasses a multi-dimensional discovery platform, and its pipeline spans both clinical-stage and preclinical programs. The clinical-stage pipeline centers on precision/targeted oncology candidates including Pimicotinib (CSF-1R inhibitor, partnered globally with Merck KGaA and already approved in China), Irpagratinib (FGFR4 inhibitor with global rights), Fexagratinib (pan-FGFR inhibitor partnered with BeiGene), ABSK061 (FGFR2/3 inhibitor), and Mavorixafor (CXCR4 antagonist partnered with X4 Pharmaceuticals for ex-China), alongside immuno-oncology assets such as ABSK043 (oral PD-L1 inhibitor) and ABSK051 (CD73 inhibitor). Multiple programs have received regulatory designations including BTD from FDA/CDE and PRIME from EMA.

Product and service12 records
1Pimicotinib (ABSK021)
CategoryPrecision / Targeted Oncology
Description

Novel oral highly selective and potent CSF-1R inhibitor approved in China for treating tenosynovial giant cell tumor (TGCT), with additional development in chronic graft-versus-host disease (cGVHD) and various solid tumors. Licensed to Merck KGaA for worldwide commercialization.

2Irpagratinib (ABSK011)
CategoryPrecision / Targeted Oncology
Description

FGFR4 inhibitor for treating FGF19-overexpressing hepatocellular carcinoma (HCC), both as monotherapy and in combination with atezolizumab. Global rights retained by Abbisko.

3Fexagratinib (ABSK091)
CategoryPrecision / Targeted Oncology
Description

Pan-FGFR inhibitor for treating FGFR-altered urothelial cancer (UC), in monotherapy and in combination with tislelizumab (partnered with BeiGene).

4ABSK061
CategoryPrecision / Targeted Oncology
Description

Selective FGFR2/3 inhibitor in development for solid tumors (combo) and achondroplasia in children. Received FDA IND clearance, orphan drug designation, and rare pediatric disease designation.

5ABSK121
CategoryPrecision / Targeted Oncology
Description

FGFR-resistant mutations inhibitor targeting solid tumors resistant to prior FGFR therapies.

6ABSK112
CategoryPrecision / Targeted Oncology
Description

EGFR Exon20 inhibitor for non-small cell lung cancer (NSCLC), representing a next-generation approach to EGFR mutation targeting.

7ABSK012
CategoryPrecision / Targeted Oncology
Description

FGFR4 mutations inhibitor in development for rhabdomyosarcoma (RMS) and solid tumors.

8ABK3376 (AST2303)
CategoryPrecision / Targeted Oncology
Description

EGFR C797S inhibitor for EGFR-mutant NSCLC, partnered with Ailis (Greater China: Ailis; Ex-China: Abbisko). Licensed to Ailis for Greater China development and commercialization.

9ABSK131
CategoryPrecision / Targeted Oncology
Description

MTA-cooperative PRMT5 inhibitor in development for solid tumors, leveraging synthetic lethality mechanism.

10Mavorixafor (ABSK081)
CategoryOther / Immuno-Oncology
Description

Oral CXCR4 antagonist for treating WHIM syndrome (Warts, Hypogammaglobulinemia, Infections, and Myelokathexis). Licensed to X4 Pharmaceuticals for ex-China markets (X4 obtained FDA approval for Xolremdi). Abbisko holds Greater China rights.

11ABSK043
CategoryOther / Immuno-Oncology
Description

Oral PD-L1 inhibitor for non-small cell lung cancer (NSCLC), in development as monotherapy and in combination with furmonertinib.

12ABSK051
CategoryOther / Immuno-Oncology
Description

CD73 inhibitor for immuno-oncology applications, targeting the adenosine pathway in tumor microenvironments.

Scale indicator3 records

Each record includes

Type, Value, Description, Source

Partnership9 partners
Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2026-01-01
Description

Abbisko entered an initial collaboration with Eli Lilly in 2022 for the development of pimicotinib (ABSK021), a CSF-1R inhibitor. In 2026, the partnership was substantially expanded, with potential deal value reaching up to $1.9 billion, covering global ex-China development and commercialization rights for pimicotinib and another undisclosed asset. Abbisko retains Greater China rights. The deal includes upfront, development, regulatory, and commercial milestones plus royalties on net sales.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Abbisko partnered with Merck KGaA for the worldwide commercialization of pimicotinib (ABSK021), leveraging Merck KGaA's global oncology commercial infrastructure. Merck KGaA handles regulatory submissions and commercialization in major markets globally.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Abbisko granted BeiGene Greater China rights for ABSK091 (pan-FGFR/WEE1 inhibitor). BeiGene is also evaluating ABSK091 in combination with its anti-PD-1 antibody tislelizumab (tislelizumab-jsgr) in patients with FGFR-altered solid tumors, representing a biomarker-driven combination therapy approach.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

AstraZeneca holds regional rights to ABSK011 (FGFR4 inhibitor, partnered for regional development and commercialization) and to AZD4547 (FGFR1/2/3 inhibitor, in-licensed by Abbisko from Roche and sub-licensed to AstraZeneca). AstraZeneca brings its global oncology capabilities to these FGFR-targeted assets.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Roche holds regional rights for ABSK011 (FGFR4 inhibitor), complementing its broader oncology portfolio. Abbisko in-licensed AZD4547 (FGFR1/2/3 inhibitor) from Roche, demonstrating the company's strategy of accessing validated assets from global pharma.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Abbisko partnered with X4 Pharmaceuticals for the development of mavorixafor in WHIM syndrome (Warts, Hypogammaglobulinemia, Infections, and Myelokathexis), a rare immune deficiency disorder. This partnership diversifies Abbisko's rare disease portfolio beyond CNS indications.

7Aileisi
Strategic tierMinorTypeOEM/ Whitelabel/ Licensing Partner
Description

Abbisko licensed ABK3376 (EGFR inhibitor) to Aileisi for development and commercialization in Greater China. Aileisi is responsible for all regulatory and commercial activities for this asset within the Chinese market.

8Shuofang Pharma
Strategic tierMinorTypeStrategic or Co-development Partner
Description

Abbisko partnered with Shuofang Pharma for the development of ABSK021 (CSF-1R inhibitor) in CNS rare disease indications within Greater China. This partnership extends the application of ABSK021 beyond its primary oncology indication (TGCT) into rare neurological diseases.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Abbisko entered a biosimilar partnership with 2seventy Bio, expanding its pipeline beyond proprietary novel small molecule oncology candidates into the biosimilar space, providing a complementary revenue stream and pipeline diversification.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage precision oncology company developing small molecule inhibitors targeting the RAS/MAPK pathway including KRAS and EGFR combinations. Comparable pipeline focus and small molecule oncology development model to Abbisko.

TypeDirect peer
Description

Hong Kong-listed (HKEX:13) clinical-stage biopharma developing precision oncology and immunology small molecules, with established global pharma partnerships (AstraZeneca, Eli Lilly, Takeda). Same Chinese-domiciled, HKEX-listed, small-molecule precision oncology profile and partnership-driven business model.

TypeDirect peer
Description

Global oncology company developing small molecule and biologic therapies, partnered with Abbisko on ABSK091 plus tislelizumab combination. Direct competitor/partner in FGFR-altered cancers and similar Chinese oncology biotech with global commercial footprint.

TypeEmerging player
Description

Clinical-stage precision therapy company developing kinase inhibitors for rare diseases and oncology indications including bezuclastinib for systemic mastocytosis. Comparable stage and rare disease/specialty oncology focus relevant to Abbisko's TGCT and rare disease programs.

TypeBroad incumbent
Description

Larger established Chinese pharmaceutical company developing both innovative branded drugs and generics across oncology, CNS, and other therapeutic areas. Provides comparison for Abbisko's scaling path from clinical-stage innovator to commercial-stage pharma.

TypeBroad incumbent
Description

Global pharmaceutical company that developed TURALIO (pexidartinib), the first FDA-approved systemic therapy for TGCT. Relevant competitor and commercial benchmark for Abbisko's pimicotinib TGCT launch trajectory.

TypeDirect peer
Description

Precision therapy company developing kinase inhibitors for genomically defined cancers and rare diseases including FGFR4 inhibitor (fisogatinib/BLU-554) and other targeted oncology assets. Highly comparable pipeline structure and indication targeting to Abbisko.

TypeDirect peer
Description

HKEX-listed Chinese biopharmaceutical company developing oncology therapies including small molecules and biologics with extensive global pharma partnerships (Eli Lilly, Roche, Sanofi). Comparable scale and pipeline breadth in oncology with strong BD track record.

TypeDirect peer
Description

Precision oncology biotech developing small molecule KRAS inhibitors (adagrasib, MRTX1133 for KRAS G12D). Direct pipeline overlap with Abbisko's KRAS G12D program (ABSK141) and Pan-KRAS (P021) initiatives.

TypeDirect peer
Description

Shanghai-based, HKEX-listed (1877.HK) biopharma focused on immuno-oncology and small molecule oncology drugs with global licensing partnerships (Eli Lilly, Coherus). Same Chinese precision/immuno-oncology model with PD-1/PD-L1 and combination therapy focus overlapping ABSK043.

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 risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Segment2 records

Each record includes

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

Ideal customer profile1 record

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

Feature12 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles5 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 rounds4 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 →

Abbisko Therapeutics

Precision Oncology Pharmaceuticalsabbisko.com

Abbisko Therapeutics is a Shanghai-based, HKEX-listed clinical-stage biopharmaceutical company that discovers and develops differentiated small-molecule therapies for precision oncology, immuno-oncology, and rare diseases, out-licensing regional and global rights to top-tier pharma partners while retaining Greater China rights.

What Abbisko Therapeutics does

Abbisko Therapeutics is a Shanghai-based, HKEX-listed (02256.HK) clinical-stage biopharmaceutical company founded in 2016 by pharma veterans including Dr. Yao-Chang Xu (former Eli Lilly) and Dr. Hongping Yu. The company focuses on discovering and developing differentiated small-molecule therapies for precision oncology, immuno-oncology, and rare diseases, with a pipeline of 11+ candidates spanning FGFR (ABSK011/irpagratinib, ABSK091/fexagratinib, ABSK061, ABSK121, ABSK012), CSF-1R (ABSK021/pimicotinib), EGFR (ABSK112, ABK3376), CXCR4 (mavorixafor/ABSK081), oral PD-L1 (ABSK043), CD73 (ABSK051), PRMT5 (ABSK131), and preclinical KRAS G12D and pan-KRAS programs. The business model is asset-light and partnership-driven: Abbisko retains Greater China rights for key assets while out-licensing regional and global ex-China development and commercialization to top-tier pharma partners (Eli Lilly, Merck KGaA, AstraZeneca, Roche, BeiGene, X4 Pharmaceuticals, Aileisi), generating revenue through upfront payments, development/regulatory/commercial milestones, and tiered royalties on net sales. The company achieved its first regulatory approval in December 2025 with China NMPA's approval of pimicotinib for tenosynovial giant cell tumor, followed by FDA NDA acceptance in January 2026; a 2026 expansion of the Eli Lilly collaboration represents up to $1.9 billion in potential milestones, signaling a transition from clinical development to early commercialization across China, the US, and Europe.

Abbisko Therapeutics firmographics

Firmographics
Name
Abbisko Therapeutics
Legal name
Abbisko Therapeutics Co., Ltd.
Website
https://abbisko.com
Company type
Public
Founded year
2016
Operating status
Operating
Headcount range
51–100 employees
Short description
Abbisko Therapeutics is a Shanghai-based, HKEX-listed clinical-stage biopharmaceutical company that discovers and develops differentiated small-molecule therapies for precision oncology, immuno-oncology, and rare diseases, out-licensing regional and global rights to top-tier pharma partners while retaining Greater China rights.
Ownership category
akta.pro rank

Abbisko Therapeutics industry classification

Industry
Product category
Precision Oncology Pharmaceuticals
NAICS
Pharmaceutical and Medicine Manufacturing (3254), Research and Development in Biotechnology (except Nanobiotechnology) (541714), Pharmaceutical Preparation Manufacturing (325412)
SIC
Pharmaceutical Preparations (2834), Medicinal Chemicals & Botanical Products (2833)
akta.pro primary industry
Oncology & Hematology Pharmaceuticals (HLAIAAAC)
akta.pro secondary industries
Rare Oncology & Hematologic Malignancy Therapies (HLAIAIAC), Oncology Specialty Pharmaceuticals (HLAIACAA), Specialty Care Pharmaceuticals (HLAIAAAB)

Keywords

  • Precision oncology drugs
  • Small molecule therapeutics
  • Targeted cancer therapy
  • FGFR inhibitors
  • Immuno-oncology drugs

Where Abbisko Therapeutics is headquartered

Location

Headquarters

HQ city
Shanghai
HQ country
China
HQ region
Asia

Offices3 records

Markets served

Abbisko Therapeutics business model

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

Revenue model

  1. Licensing and Milestone Payments: Abbisko generates revenue through licensing deals in which it grants regional or global rights to its pipeline assets in exchange for upfront payments, development and regulatory milestone payments, and commercial milestone payments. The 2022 Eli Lilly collaboration and its 2026 $1.9 billion expansion represent the flagship example. Milestone payments are triggered upon achievement of clinical, regulatory, and commercial milestones.
  2. Royalties on Net Sales: Following regulatory approval and commercialization of licensed assets, Abbisko receives royalty payments on net sales from its commercialization partners. Royalties provide recurring revenue tied to commercial performance of approved therapies in partnered territories.

Go-to-market motion1 record

Distribution channels7 records

Marketing channels3 records

Abbisko Therapeutics product offering

Product offering

Core offering

Abbisko Therapeutics discovers and develops differentiated small-molecule therapies for cancer and rare diseases, with a pipeline of 15+ clinical-stage and preclinical programs targeting FGFR, CSF-1R, KRAS, EGFR, PD-L1, CD73, and other oncology mechanisms. The company pursues a partnership-driven commercialization model, out-licensing global or regional rights to major pharmaceutical partners while retaining rights in Greater China for select assets.

Product overview

Abbisko Therapeutics is a Shanghai-based clinical-stage biopharmaceutical company founded in 2016, focused on discovering and developing novel and differentiated small-molecule therapies for cancer and beyond. The company's in-house R&D engine encompasses a multi-dimensional discovery platform, and its pipeline spans both clinical-stage and preclinical programs. The clinical-stage pipeline centers on precision/targeted oncology candidates including Pimicotinib (CSF-1R inhibitor, partnered globally with Merck KGaA and already approved in China), Irpagratinib (FGFR4 inhibitor with global rights), Fexagratinib (pan-FGFR inhibitor partnered with BeiGene), ABSK061 (FGFR2/3 inhibitor), and Mavorixafor (CXCR4 antagonist partnered with X4 Pharmaceuticals for ex-China), alongside immuno-oncology assets such as ABSK043 (oral PD-L1 inhibitor) and ABSK051 (CD73 inhibitor). Multiple programs have received regulatory designations including BTD from FDA/CDE and PRIME from EMA.

Differentiator

Problem solved

Functional benefit

Brands

  • 贝捷迈® (Pimicotinib): Brand name for Pimicotinib (ABSK021), the company's CSF-1R inhibitor approved in China for tenosynovial giant cell tumor.

Products and services

  • Pimicotinib (ABSK021) Novel oral highly selective and potent CSF-1R inhibitor approved in China for treating tenosynovial giant cell tumor (TGCT), with additional development in chronic graft-versus-host disease (cGVHD) and various solid tumors. Licensed to Merck KGaA for worldwide commercialization.
  • Irpagratinib (ABSK011) FGFR4 inhibitor for treating FGF19-overexpressing hepatocellular carcinoma (HCC), both as monotherapy and in combination with atezolizumab. Global rights retained by Abbisko.
  • Fexagratinib (ABSK091) Pan-FGFR inhibitor for treating FGFR-altered urothelial cancer (UC), in monotherapy and in combination with tislelizumab (partnered with BeiGene).
  • ABSK061 Selective FGFR2/3 inhibitor in development for solid tumors (combo) and achondroplasia in children. Received FDA IND clearance, orphan drug designation, and rare pediatric disease designation.
  • ABSK121 FGFR-resistant mutations inhibitor targeting solid tumors resistant to prior FGFR therapies.
  • ABSK112 EGFR Exon20 inhibitor for non-small cell lung cancer (NSCLC), representing a next-generation approach to EGFR mutation targeting.
  • ABSK012 FGFR4 mutations inhibitor in development for rhabdomyosarcoma (RMS) and solid tumors.
  • ABK3376 (AST2303) EGFR C797S inhibitor for EGFR-mutant NSCLC, partnered with Ailis (Greater China: Ailis; Ex-China: Abbisko). Licensed to Ailis for Greater China development and commercialization.
  • ABSK131 MTA-cooperative PRMT5 inhibitor in development for solid tumors, leveraging synthetic lethality mechanism.
  • Mavorixafor (ABSK081) Oral CXCR4 antagonist for treating WHIM syndrome (Warts, Hypogammaglobulinemia, Infections, and Myelokathexis). Licensed to X4 Pharmaceuticals for ex-China markets (X4 obtained FDA approval for Xolremdi). Abbisko holds Greater China rights.
  • ABSK043 Oral PD-L1 inhibitor for non-small cell lung cancer (NSCLC), in development as monotherapy and in combination with furmonertinib.
  • ABSK051 CD73 inhibitor for immuno-oncology applications, targeting the adenosine pathway in tumor microenvironments.

Quantifiable outcome

  • Potential deal value of up to $1.9 billion in the expanded Eli Lilly partnership for pimicotinib and another asset (2026)
  • +1 more outcomes

Companies that use Abbisko Therapeutics

Customer profile

Segments2 records

Ideal customer profiles1 record

Abbisko Therapeutics technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature12 records

Abbisko Therapeutics partnerships and signals

Strategic signal

Partnerships

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

  • Eli LillyflagshipStrategic or Co-development Partner · 1 January 2026Abbisko entered an initial collaboration with Eli Lilly in 2022 for the development of pimicotinib (ABSK021), a CSF-1R inhibitor. In 2026, the partnership was substantially expanded, with potential deal value reaching up to $1.9 billion, covering global ex-China development and commercialization rights for pimicotinib and another undisclosed asset. Abbisko retains Greater China rights. The deal includes upfront, development, regulatory, and commercial milestones plus royalties on net sales.
  • Merck KGaAcoreStrategic or Co-development PartnerAbbisko partnered with Merck KGaA for the worldwide commercialization of pimicotinib (ABSK021), leveraging Merck KGaA's global oncology commercial infrastructure. Merck KGaA handles regulatory submissions and commercialization in major markets globally.
  • BeiGenecoreStrategic or Co-development PartnerAbbisko granted BeiGene Greater China rights for ABSK091 (pan-FGFR/WEE1 inhibitor). BeiGene is also evaluating ABSK091 in combination with its anti-PD-1 antibody tislelizumab (tislelizumab-jsgr) in patients with FGFR-altered solid tumors, representing a biomarker-driven combination therapy approach.
  • AstraZenecacoreStrategic or Co-development PartnerAstraZeneca holds regional rights to ABSK011 (FGFR4 inhibitor, partnered for regional development and commercialization) and to AZD4547 (FGFR1/2/3 inhibitor, in-licensed by Abbisko from Roche and sub-licensed to AstraZeneca). AstraZeneca brings its global oncology capabilities to these FGFR-targeted assets.
  • RochecoreStrategic or Co-development PartnerRoche holds regional rights for ABSK011 (FGFR4 inhibitor), complementing its broader oncology portfolio. Abbisko in-licensed AZD4547 (FGFR1/2/3 inhibitor) from Roche, demonstrating the company's strategy of accessing validated assets from global pharma.
  • X4 PharmaceuticalsminorStrategic or Co-development PartnerAbbisko partnered with X4 Pharmaceuticals for the development of mavorixafor in WHIM syndrome (Warts, Hypogammaglobulinemia, Infections, and Myelokathexis), a rare immune deficiency disorder. This partnership diversifies Abbisko's rare disease portfolio beyond CNS indications.
  • AileisiminorOEM/ Whitelabel/ Licensing PartnerAbbisko licensed ABK3376 (EGFR inhibitor) to Aileisi for development and commercialization in Greater China. Aileisi is responsible for all regulatory and commercial activities for this asset within the Chinese market.
  • Shuofang PharmaminorStrategic or Co-development PartnerAbbisko partnered with Shuofang Pharma for the development of ABSK021 (CSF-1R inhibitor) in CNS rare disease indications within Greater China. This partnership extends the application of ABSK021 beyond its primary oncology indication (TGCT) into rare neurological diseases.
  • 2seventy BiominorStrategic or Co-development PartnerAbbisko entered a biosimilar partnership with 2seventy Bio, expanding its pipeline beyond proprietary novel small molecule oncology candidates into the biosimilar space, providing a complementary revenue stream and pipeline diversification.

Scale indicators3 records

Recent moves8 records

Expansion highlights6 records

Abbisko Therapeutics competitors and assessment

Company assessment

Direct peers

  • Erasca: Clinical-stage precision oncology company developing small molecule inhibitors targeting the RAS/MAPK pathway including KRAS and EGFR combinations. Comparable pipeline focus and small molecule oncology development model to Abbisko.
  • Hutchmed (HUTCHMED Limited): Hong Kong-listed (HKEX:13) clinical-stage biopharma developing precision oncology and immunology small molecules, with established global pharma partnerships (AstraZeneca, Eli Lilly, Takeda). Same Chinese-domiciled, HKEX-listed, small-molecule precision oncology profile and partnership-driven business model.
  • BeiGene: Global oncology company developing small molecule and biologic therapies, partnered with Abbisko on ABSK091 plus tislelizumab combination. Direct competitor/partner in FGFR-altered cancers and similar Chinese oncology biotech with global commercial footprint.
  • Blueprint Medicines: Precision therapy company developing kinase inhibitors for genomically defined cancers and rare diseases including FGFR4 inhibitor (fisogatinib/BLU-554) and other targeted oncology assets. Highly comparable pipeline structure and indication targeting to Abbisko.
  • Innovent Biologics: HKEX-listed Chinese biopharmaceutical company developing oncology therapies including small molecules and biologics with extensive global pharma partnerships (Eli Lilly, Roche, Sanofi). Comparable scale and pipeline breadth in oncology with strong BD track record.
  • Mirati Therapeutics: Precision oncology biotech developing small molecule KRAS inhibitors (adagrasib, MRTX1133 for KRAS G12D). Direct pipeline overlap with Abbisko's KRAS G12D program (ABSK141) and Pan-KRAS (P021) initiatives.
  • Junshi Biosciences: Shanghai-based, HKEX-listed (1877.HK) biopharma focused on immuno-oncology and small molecule oncology drugs with global licensing partnerships (Eli Lilly, Coherus). Same Chinese precision/immuno-oncology model with PD-1/PD-L1 and combination therapy focus overlapping ABSK043.

Emerging players

  • Cogent Biosciences: Clinical-stage precision therapy company developing kinase inhibitors for rare diseases and oncology indications including bezuclastinib for systemic mastocytosis. Comparable stage and rare disease/specialty oncology focus relevant to Abbisko's TGCT and rare disease programs.

Broad incumbents

  • Hansoh Pharmaceutical: Larger established Chinese pharmaceutical company developing both innovative branded drugs and generics across oncology, CNS, and other therapeutic areas. Provides comparison for Abbisko's scaling path from clinical-stage innovator to commercial-stage pharma.
  • Daiichi Sankyo: Global pharmaceutical company that developed TURALIO (pexidartinib), the first FDA-approved systemic therapy for TGCT. Relevant competitor and commercial benchmark for Abbisko's pimicotinib TGCT launch trajectory.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

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Frequently asked questions about Abbisko Therapeutics

What does Abbisko Therapeutics do?

Abbisko Therapeutics discovers and develops differentiated small-molecule therapies for cancer and rare diseases, with a pipeline of 15+ clinical-stage and preclinical programs targeting FGFR, CSF-1R, KRAS, EGFR, PD-L1, CD73, and other oncology mechanisms. The company pursues a partnership-driven commercialization model, out-licensing global or regional rights to major pharmaceutical partners while retaining rights in Greater China for select assets.

Is Abbisko Therapeutics a public or private company?

Abbisko Therapeutics is a public company. It is classified as public and is currently operating.

When was Abbisko Therapeutics founded?

Abbisko Therapeutics was founded in 2016. It employs 51 to 100 people.

Where is Abbisko Therapeutics based?

Abbisko Therapeutics is headquartered in Shanghai, China, in the Asia region.

How does Abbisko Therapeutics make money?

Two revenue lines are on record. Licensing and Milestone Payments are the primary driver. The others are royalties on Net Sales.

Who are Abbisko Therapeutics's main competitors?

Direct peers on record are Erasca, Hutchmed (HUTCHMED Limited), BeiGene, Blueprint Medicines, Innovent Biologics, Mirati Therapeutics and Junshi Biosciences. Cogent Biosciences is listed as an emerging player. Broad incumbents are Hansoh Pharmaceutical and Daiichi Sankyo.

Does Abbisko Therapeutics have an API?

No public API is recorded for Abbisko Therapeutics.

What industry is Abbisko Therapeutics in?

Abbisko Therapeutics's product category is Precision Oncology Pharmaceuticals. Its primary akta.pro industry code is HLAIAAAC, Oncology & Hematology Pharmaceuticals, with a secondary code of HLAIAIAC, Rare Oncology & Hematologic Malignancy Therapies. Its NAICS code is 3254 and its SIC code is 2834.

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STATIn Shanghai's 'Science City,' China's ascendant biotechs make their pitch to the worldBiotech executives in Shanghai's Science City pitched their drug development efficiency, with Abbisko's co-founder Zhui Chen citing an 11-month trial for a Merck KGaA drug. The trial finished so quickly that Merck executives asked if Abbisko could train their staff.AInvestAbbisko Therapeutics: The "Encouraging Phase II Data" Headline Is About Cancer, Not ChildrenAbbisko Therapeutics announced FDA designations for its achondroplasia drug ABSK061, but no Phase II efficacy data exists for that indication. The company reported a 90% response rate in gastric cancer with ABSK061 plus ABSK043, and its revenue fell to CNY 97 million in H1 2026. A $1.9 billion Lilly collaboration provides a revenue floor, but the investment case depends on future clinical results.Simply Wall StAbbisko Cayman (SEHK:2256) Stock Can Cheap Book Value Outrun Renewed LossesAbbisko Cayman closed at HK$9.875 on Tuesday, down roughly 4% over a week and 8% over a month, after reporting H1 2026 results. Revenue fell to C¥97.265 million from C¥612.119 million, and net income swung to a loss of C¥193.466 million, with trailing 12-month losses of C¥466.691 million. The article frames the stock as a deep value opportunity at a 64.5% discount to DCF fair value.AijournAbbisko Therapeutics and AstraZeneca Enter a Strategic Collaboration to Conduct the Clinical Trial of Lumipodlin (ABSK043), a First-in-Class Oral PD-L1 Inhibitor, in Combination with TAGRISSO® for NSCAbbisko Therapeutics announced a strategic collaboration with AstraZeneca to jointly advance a Phase I/II clinical study evaluating lumipodlin (ABSK043), Abbisko's first-in-class oral PD-L1 inhibitor, in combination with AstraZeneca's TAGRISSO (osimertinib) for EGFR-mutated, PD-L1 positive locally advanced or metastatic non-small cell lung cancer. The investigational new drug application for the combination study was cleared by China's National Medical Products Administration on May 20, 2026, and the Phase II study will be led by Abbisko with shared responsibilities between both companies. The combination addresses a long-standing unmet medical need, as EGFR-mutant patients with high PD-L1 expression derive less benefit from EGFR-TKIs alone.PR Newswire APACAbbisko Therapeutics and AstraZeneca Enter a Strategic Collaboration to Conduct the Clinical Trial of Lumipodlin (ABSK043), a First-in-Class Oral PD-L1 Inhibitor, in Combination with TAGRISSO® for NSCAbbisko Therapeutics and AstraZeneca announced a strategic collaboration to jointly conduct a multicenter Phase I/II clinical study evaluating the combination of Abbisko's first-in-class oral PD-L1 inhibitor lumipodlin (ABSK043) with AstraZeneca's third-generation EGFR-TKI TAGRISSO® (osimertinib) for EGFR-mutated, PD-L1 positive locally advanced or metastatic non-small cell lung cancer (NSCLC). The investigational new drug application for the combination study was cleared by China's National Medical Products Administration on May 20, 2026, with both companies sharing clinical trial responsibilities. The collaboration aims to address an unmet medical need, as EGFR-mutant patients with high PD-L1 expression derive limited benefit from EGFR-TKIs alone.PR NewswireAbbisko Therapeutics and AstraZeneca Enter a Strategic Collaboration to Conduct the Clinical Trial of Lumipodlin (ABSK043), a First-in-Class Oral PD-L1 Inhibitor, in Combination with TAGRISSO® for NSCAbbisko Therapeutics has entered into a strategic collaboration with AstraZeneca to jointly conduct a Phase I/II clinical trial combining lumipodlin (ABSK043), Abbisko's first-in-class oral PD-L1 inhibitor, with AstraZeneca's TAGRISSO (osimertinib) for the treatment of EGFR-mutated, PD-L1 positive locally advanced or metastatic non-small cell lung cancer (NSCLC). The investigational new drug application for this combination therapy was cleared by China's National Medical Products Administration on May 20, 2026, and both companies will share clinical trial responsibilities in this multicenter, open-label study. This combination addresses a significant unmet medical need, as EGFR-mutated NSCLC patients with high PD-L1 expression derive less clinical benefit from EGFR-TKI monotherapy.Clinical Trials ArenaAstraZeneca and Abbisko collaborate on NSCLC combination therapy trialAstraZeneca and Abbisko signed a collaboration to study Tagrisso and lumipodlin in NSCLC patients with EGFR mutations and PD-L1 positivity. The Phase I/II trial's IND was cleared by China's NMPA on 20 May 2026, with Abbisko leading. Lumipodlin is an oral PD-L1 inhibitor under investigation in Australia and China.BioSpaceLilly deepens relationship with China’s Abbisko for $1.9B biobucksEli Lilly has expanded its partnership with Shanghai-based Abbisko Therapeutics, with potential payments of up to $1.9 billion covering upfront, development, regulatory, and commercial milestones plus tiered royalties on any approved therapies. This builds on a prior 2022 collaboration between the companies worth up to $258 million for a cardiometabolic target. Lilly has emerged as pharma's top M&A spender in 2026, with commitments totaling over $25 billion including acquisitions such as Centessa ($6.3B), Kelonia ($7B), Orna ($2.4B), Ajax ($2.3B), and multiple vaccine biotechs.The Pharma LetterAbbisko Thera deepens R&D collaboration with LillyChinese biotech company Abbisko Therapeutics has entered into a strategic research collaboration and license agreement with US pharma major Eli Lilly to discover and develop innovative medicines across multiple targets with global potential. The collaboration leverages Abbisko's and Eli Lilly's respective strengths in drug discovery, research and development, and global drug development to advance novel therapeutic programs. Both companies aim to accelerate the progression of innovative treatments and bring new options to patients worldwide.GurufocusAbbisko Therapeutics Deepens R&D Collaboration with LillyAbbisko Therapeutics has entered into a strategic research collaboration and license agreement with Eli Lilly and Company for the discovery and development of innovative medicines across multiple targets. Under the deal, Abbisko will leverage its early-stage drug discovery platform to conduct discovery and early development activities for novel drug programs directed against disease targets selected by Lilly. Abbisko will receive an upfront payment and is eligible to receive development, regulatory and commercial milestone payments totaling up to approximately US$1.9 billion, plus tiered royalties based on annual net sales of products arising from the collaboration.