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ABL Bio

Full company profile

uuid0000z3e

Namestring
ABL Bio
Legal namestring
ABL Bio, Inc.
Websiteurl
ablbio.com
Company typeenum
Public
Founded yearint
2016
Descriptiontext

ABL Bio is a South Korea-based clinical-stage biotechnology company founded in 2016 and listed on the KOSDAQ exchange (ticker 298380). The company specializes in the discovery and development of bispecific antibody therapeutics, with primary focus areas in immuno-oncology and neurodegenerative diseases. ABL Bio's core technology rests on three proprietary platforms: Grabody-T (4-1BB agonism for oncology), Grabody-B (blood-brain barrier shuttle for CNS-targeted therapeutics), and Grabody-I (immune checkpoint modulation). The company is also developing bispecific antibody-drug conjugates (ADCs) using N-terminal selective conjugation technology, which has been spun out into NEOK Bio. Its clinical pipeline includes givastomig (CLDN18.2 x 4-1BB, partnered with Compass Therapeutics), tovecimig (4-1BB x 5T4), and ABL301 (alpha-synuclein x IGF1R for Parkinson's disease, partnered with Sanofi).

ABL Bio operates a B2B out-licensing business model, monetizing its platforms and pipeline assets through upfront payments, milestone payments, and royalties from global pharmaceutical partners rather than through direct product commercialization. Headline deal value across disclosed partnerships exceeds $6 billion (Sanofi $1.06B in 2022, GSK $2.5B in 2025, Eli Lilly $2.6B in 2025), though the vast majority of these figures are back-end-loaded milestone and royalty potential. Upfront cash receipts, equity investments, and milestone payments drive near-term revenue, which is inherently lumpy. The company has also secured U.S. regulatory designations — FDA Fast Track and Orphan Drug status for both givastomig and tovecimig — which materially de-risk the lead oncology assets and strengthen partner economics. ABL Bio is headquartered in Seongnam, South Korea, with 51-100 employees, and has begun expanding its U.S. footprint via the NEOK Bio spin-off and strategic equity from Eli Lilly.

Short descriptiontext

ABL Bio is a South Korean clinical-stage biotech developing bispecific antibody therapeutics in oncology and neurodegenerative diseases via proprietary Grabody platforms, monetized primarily through out-licensing deals with global pharmaceutical partners such as Sanofi, Eli Lilly, and GSK.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersSeongnam, South Korea
HQ citystring
Seongnam
HQ countrystring
South Korea
HQ regionstring
Asia
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
bispecific antibody therapeutics, immuno-oncology drug development, neurodegenerative disease therapeutics, antibody-drug conjugates, biotechnology platform licensing
Industry2 codes
1Regulatory Strategy & IND/NDA/BLA Submissions Support
CodeHLAIALAHPrimaryYes
2Clinical Trial Pharmacy & IMP Management at Site
CodeHLAGACAKPrimaryNo
NAICS code1 code
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Bispecific Antibody Therapeutics & Platform Licensing
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model3 records
1Technology Licensing
TypeLicensing Royalties
Description

ABL Bio licenses its bispecific antibody platforms and pipeline candidates to global pharmaceutical companies. Deals include upfront payments, milestone payments tied to development and regulatory achievements, and royalty payments on product sales. Notable deals include GSK ($2.5B for neurodegenerative diseases), Eli Lilly ($2.6B for Grabody platform), Sanofi ($1.06B for ABL301).

biospace.com
2Milestone Payments
TypeLicensing Royalties
Description

Development milestone payments received upon achievement of specific clinical, regulatory, and commercial milestones. Examples include $40M upfront + $15M equity from Lilly, $7.5M upfront from Sanofi for ABL301, and various milestone payments from Compass Therapeutics for ABL001 progress.

biospace.com
3Royalty Revenue
TypeLicensing Royalties
Description

Future royalty payments anticipated from commercialized products developed through partnerships. CEO projected that ABL001 royalty revenue in 2027 will significantly transform the company's financial profile.

healthcareasiamagazine.com
Marketing channels4 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 typeServices
Services
Brand1 of 3 records shown
1Grabody-T
Description

4-1BB based bispecific antibody platform for immuno-oncology that activates T cells only in tumor microenvironment

ablbio.com
+2 more records
Core offering1 text field

ABL Bio is a clinical-stage biotechnology company that develops proprietary bispecific antibody therapeutic platforms and pipeline candidates for immuno-oncology, neurodegenerative diseases, and antibody-drug conjugates. The company generates revenue primarily by licensing its Grabody-T, Grabody-B, and Grabody-I platforms and pipeline assets (such as ABL111, ABL503, ABL301, ABL001) to global pharmaceutical partners via upfront payments, milestone payments, and royalties.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • 75% objective response rate (ORR) and 16.9-month median progression-free survival for givastomig (ABL111) in Phase 1b trial
+5 more records
Product overview1 text field

ABL Bio is a South Korean bispecific antibody biotech company with three proprietary platform technologies: Grabody-T (4-1BB-based immuno-oncology platform), Grabody-I (immune checkpoint bispecific platform), and Grabody-B (BBB shuttle platform for neurodegenerative diseases). The company operates a diverse pipeline including clinical candidates like Givastomig (ABL111) for gastric cancer, Ragistomig (ABL503), ABL501, and ABL301 (licensed to Sanofi for Parkinson's). Their ADC programs include ABL206 and ABL209 being developed through subsidiary NEOK Bio. Multiple programs are partnered with global pharma including Eli Lilly (Grabody-B), GSK (BBB platform), Sanofi (ABL301), and Compass Therapeutics (ABL001).

Product and service13 records
1Grabody-T Platform
CategoryBispecific Antibody Platform
Description

A 4-1BB-based bispecific antibody platform that activates T cells only in tumor microenvironments where tumor antigens are present, minimizing systemic toxicity associated with traditional 4-1BB immunotherapy. Licensed to global pharmaceutical partners as a development engine.

2Grabody-B Platform
CategoryBispecific Antibody Platform
Description

A blood-brain barrier (BBB) shuttle platform that uses IGF1R targeting to maximize delivery of therapeutic antibodies into the brain for treatment of neurodegenerative diseases. Achieves 7x or higher BBB penetration versus monoclonal antibodies in preclinical studies.

3Grabody-I Platform
CategoryBispecific Antibody Platform
Description

An immune checkpoint bispecific antibody platform designed to overcome limitations of conventional PD-(L)1 therapy by targeting multiple immune checkpoint pathways.

4Givastomig (ABL111)
CategoryClinical Candidate (Bispecific Antibody)
Description

Bispecific antibody targeting Claudin 18.2 and 4-1BB for treatment of gastric cancer, jointly developed with NovaBridge Biosciences. Received FDA Fast Track and Orphan Drug designations. Demonstrated 75% objective response rate and 16.9-month median progression-free survival in Phase 1b trial.

5Ragistomig (ABL503)
CategoryClinical Candidate (Bispecific Antibody)
Description

Bispecific antibody targeting PD-L1 and 4-1BB for immuno-oncology applications, designed to minimize 4-1BB toxicity while augmenting T-cell activation. Jointly developed with NovaBridge Biosciences.

6ABL501
CategoryClinical Candidate (Bispecific Antibody)
Description

Bispecific antibody targeting LAG-3 and PD-L1 immune checkpoint pathways to overcome resistance and low response rates in conventional PD-(L)1 therapy.

7ABL301 (SAR446159)
CategoryClinical Candidate (Bispecific Antibody)
Description

Bispecific antibody for Parkinson's disease using Grabody-B platform to deliver alpha-synuclein targeting antibodies across the blood-brain barrier. Licensed to Sanofi for global development.

8ABL001 (Tovecimig)
CategoryClinical Candidate (Bispecific Antibody)
Description

Bispecific antibody targeting VEGF and DLL4 for treatment of solid tumors, particularly biliary tract cancer. Licensed to Compass Therapeutics.

9ABL206 (NEOK001)
CategoryClinical Candidate (Bispecific ADC)
Description

First-in-class bispecific ADC targeting B7-H3 and ROR1 with topoisomerase I inhibitor payload, developed through NEOK Bio subsidiary for advanced solid tumors.

10ABL209 (NEOK002)
CategoryClinical Candidate (Bispecific ADC)
Description

Bispecific ADC targeting EGFR and MUC1 with topoisomerase I inhibitor payload, developed through NEOK Bio subsidiary for advanced solid tumors.

11ABL105 (Nesfrotamig)
CategoryClinical Candidate (Bispecific Antibody)
Description

Bispecific antibody targeting HER2 and 4-1BB for solid tumor treatment, licensed to Yuhan Corporation for Korea and Australia development.

12ABL103
CategoryClinical Candidate (Bispecific Antibody)
Description

Bispecific antibody targeting B7-H4 and 4-1BB for solid cancer treatment, designed to activate T cells only in B7-H4 expressing tumor microenvironments.

13ABL202 (CS5001/LCB71)
CategoryClinical Candidate (ADC)
Description

ROR1-targeting ADC developed in partnership with LegoChem Biosciences and licensed to CStone Pharmaceuticals for global development excluding Korea.

Scale indicator13 records

Each record includes

Type, Value, Description, Source

Partnership13 partners
Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2025-12-26
Description

Licensing, research, and collaboration agreement for Grabody platform worth $2.6 billion total. ABL Bio received $40 million upfront payment and $15 million equity investment from Lilly. The agreement aims to advance the Grabody platform for therapeutic development in areas including obesity and muscle disorders.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-11-01
Description

ABL Bio's US subsidiary developing bispecific ADCs ABL206 (NEOK001) and ABL209 (NEOK002). Launched with $75M Series A financing led by ABL Bio. Phase 1 clinical trials initiated.

Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2025-04-01
Description

$2.5 billion licensing agreement for development of therapies for neurodegenerative diseases using Grabody platform.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2024-07-01
Description

Clinical trial collaboration and supply agreement for ABL103 with KEYTRUDA (pembrolizumab) combination therapy in advanced/metastatic solid tumors.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2024-01-01
Description

Linker-payload technology licensing agreement for next-generation bispecific ADC development.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2024-01-01
Description

Linker-payload technology partnership for bispecific ADC development.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2022-05-15
Description

Collaboration on siRNA and Grabody-B conjugation demonstrating delivery to cerebellum and various brain regions, muscle, heart, and lungs. Research presented at TIDES USA 2026.

Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2022-01-01
Description

$1.06 billion co-development and licensing agreement for ABL301 (Parkinson's disease treatment using Grabody-B platform). Includes $750M upfront payment and milestones. Sanofi responsible for Phase 2+ clinical development.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2022-01-01
Description

Licensed ABL105 (HER2x4-1BB) for development in Korea and Australia. Phase 1/2 clinical trial being conducted by Yuhan.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2021-03-30
Description

Joint development of ABL111 (Givastomig) targeting Claudin 18.2 and 4-1BB for gastric cancer; ABL503 (Ragistomig) targeting PD-L1 and 4-1BB for solid tumors. FDA Fast Track designation obtained for givastomig.

Strategic tierCoreTypeTechnology or IntegrationAnnounced on2020-11-02
Description

Expanded ADC technology cooperation including bispecific antibody ADCs. Previously successful licensing of ABL202 (LCB71) to CStone. Four joint projects ongoing including next-generation ADC development.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2020-10-01
Description

Licensed ABL202 (ROR1 ADC, CS5001/LCB71) for global development excluding Korea. $117M exclusive China licensing deal by TRIGR and Elpiscience included this asset.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2018-01-01
Description

Licensed ABL001 (Tovecimig) for global development excluding Korea and Greater China. Compass conducting Phase 2/3 COMPANION-002 trial in biliary tract cancer. FDA Fast Track and Orphan Drug designations obtained.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage biotech developing engineered bispecific antibodies using the XmAb platform, with multiple pharma partnerships and pipeline assets in oncology. Comparable technology platform and licensing-based business model.

TypeDirect peer
Description

Clinical-stage oncology biotech developing bispecific antibodies (e.g., vobramitamig duocarmazine, enoblituzumab) with multiple Big Pharma partnerships. Comparable in pipeline scope and target indications.

TypeDirect peer
Description

Biotech developing BBB-penetrant therapeutics for neurodegenerative diseases, sharing ABL Bio's Grabody-B strategic focus. Closely comparable in CNS delivery technology and target indications (Parkinson's, Alzheimer's).

TypeDirect peer
Description

Developed T cell-engaging bispecific antibodies using the COBRA platform. Highly comparable technology approach (conditional 4-1BB-like activation) and was acquired by Takeda in 2021, representing a potential exit path for ABL Bio.

TypeDirect peer
Description

Danish biotech pioneer in bispecific antibody technology with the proprietary DuoBody platform. Most directly comparable peer in technology, business model (platform licensing), and target indications (immuno-oncology).

TypeDirect peer
Description

Clinical-stage bispecific antibody developer and ABL Bio's licensee for ABL001 (Tovecimig). Direct operating peer with overlapping pipeline in oncology and similar partnership-driven model.

TypeDirect peer
Description

Clinical-stage biotech with the Azymetric and ZymeLink platforms for bispecific antibodies and ADCs. Direct competitor in both bispecific antibody and ADC spaces with similar licensing-driven revenue model.

TypeDirect peer
Description

Korean biotech developing ADCs including the LCB71 (ABL202) platform that ABL Bio licensed to CStone. Direct technology partner and Korean biotech peer with overlapping ADC pipeline.

TypeEmerging player
Description

Co-development partner on ABL111 (Givastomig) and ABL503 (Ragistomig). Asian emerging biotech with comparable bispecific antibody pipeline and strategic transformation plans relevant to ABL Bio's growth model.

TypeDirect peer
Description

Developed T cell engagers and bispecific antibodies including HPN328. Acquired by Merck for $680M in 2024, providing a relevant M&A comparable for ABL Bio's platform-licensing business model.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

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Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks6 records

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Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers8 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 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

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles2 records

Each record includes

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

Subsidiaries2 records

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

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds5 records

Each record includes

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

Investors11 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

Investment2 records

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 →

ABL Bio

Bispecific Antibody Therapeutics & Platform Licensingablbio.com

ABL Bio is a South Korean clinical-stage biotech developing bispecific antibody therapeutics in oncology and neurodegenerative diseases via proprietary Grabody platforms, monetized primarily through out-licensing deals with global pharmaceutical partners such as Sanofi, Eli Lilly, and GSK.

What ABL Bio does

ABL Bio is a South Korea-based clinical-stage biotechnology company founded in 2016 and listed on the KOSDAQ exchange (ticker 298380). The company specializes in the discovery and development of bispecific antibody therapeutics, with primary focus areas in immuno-oncology and neurodegenerative diseases. ABL Bio's core technology rests on three proprietary platforms: Grabody-T (4-1BB agonism for oncology), Grabody-B (blood-brain barrier shuttle for CNS-targeted therapeutics), and Grabody-I (immune checkpoint modulation). The company is also developing bispecific antibody-drug conjugates (ADCs) using N-terminal selective conjugation technology, which has been spun out into NEOK Bio. Its clinical pipeline includes givastomig (CLDN18.2 x 4-1BB, partnered with Compass Therapeutics), tovecimig (4-1BB x 5T4), and ABL301 (alpha-synuclein x IGF1R for Parkinson's disease, partnered with Sanofi).

ABL Bio operates a B2B out-licensing business model, monetizing its platforms and pipeline assets through upfront payments, milestone payments, and royalties from global pharmaceutical partners rather than through direct product commercialization. Headline deal value across disclosed partnerships exceeds $6 billion (Sanofi $1.06B in 2022, GSK $2.5B in 2025, Eli Lilly $2.6B in 2025), though the vast majority of these figures are back-end-loaded milestone and royalty potential. Upfront cash receipts, equity investments, and milestone payments drive near-term revenue, which is inherently lumpy. The company has also secured U.S. regulatory designations — FDA Fast Track and Orphan Drug status for both givastomig and tovecimig — which materially de-risk the lead oncology assets and strengthen partner economics. ABL Bio is headquartered in Seongnam, South Korea, with 51-100 employees, and has begun expanding its U.S. footprint via the NEOK Bio spin-off and strategic equity from Eli Lilly.

ABL Bio firmographics

Firmographics
Name
ABL Bio
Legal name
ABL Bio, Inc.
Website
https://ablbio.com
Company type
Public
Founded year
2016
Operating status
Operating
Headcount range
51–100 employees
Short description
ABL Bio is a South Korean clinical-stage biotech developing bispecific antibody therapeutics in oncology and neurodegenerative diseases via proprietary Grabody platforms, monetized primarily through out-licensing deals with global pharmaceutical partners such as Sanofi, Eli Lilly, and GSK.
Ownership category
akta.pro rank

ABL Bio industry classification

Industry
Product category
Bispecific Antibody Therapeutics & Platform Licensing
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Regulatory Strategy & IND/NDA/BLA Submissions Support (HLAIALAH)
akta.pro secondary industry
Clinical Trial Pharmacy & IMP Management at Site (HLAGACAK)

Keywords

  • Bispecific antibody therapeutics
  • Immuno-oncology drug development
  • Neurodegenerative disease therapeutics
  • Antibody-drug conjugates
  • Biotechnology platform licensing

Where ABL Bio is headquartered

Location

Headquarters

HQ city
Seongnam
HQ country
South Korea
HQ region
Asia

Offices3 records

Markets served

ABL Bio business model

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

Revenue model

  1. Technology Licensing: ABL Bio licenses its bispecific antibody platforms and pipeline candidates to global pharmaceutical companies. Deals include upfront payments, milestone payments tied to development and regulatory achievements, and royalty payments on product sales. Notable deals include GSK ($2.5B for neurodegenerative diseases), Eli Lilly ($2.6B for Grabody platform), Sanofi ($1.06B for ABL301).
  2. Milestone Payments: Development milestone payments received upon achievement of specific clinical, regulatory, and commercial milestones. Examples include $40M upfront + $15M equity from Lilly, $7.5M upfront from Sanofi for ABL301, and various milestone payments from Compass Therapeutics for ABL001 progress.
  3. Royalty Revenue: Future royalty payments anticipated from commercialized products developed through partnerships. CEO projected that ABL001 royalty revenue in 2027 will significantly transform the company's financial profile.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels4 records

ABL Bio product offering

Product offering

Core offering

ABL Bio is a clinical-stage biotechnology company that develops proprietary bispecific antibody therapeutic platforms and pipeline candidates for immuno-oncology, neurodegenerative diseases, and antibody-drug conjugates. The company generates revenue primarily by licensing its Grabody-T, Grabody-B, and Grabody-I platforms and pipeline assets (such as ABL111, ABL503, ABL301, ABL001) to global pharmaceutical partners via upfront payments, milestone payments, and royalties.

Product overview

ABL Bio is a South Korean bispecific antibody biotech company with three proprietary platform technologies: Grabody-T (4-1BB-based immuno-oncology platform), Grabody-I (immune checkpoint bispecific platform), and Grabody-B (BBB shuttle platform for neurodegenerative diseases). The company operates a diverse pipeline including clinical candidates like Givastomig (ABL111) for gastric cancer, Ragistomig (ABL503), ABL501, and ABL301 (licensed to Sanofi for Parkinson's). Their ADC programs include ABL206 and ABL209 being developed through subsidiary NEOK Bio. Multiple programs are partnered with global pharma including Eli Lilly (Grabody-B), GSK (BBB platform), Sanofi (ABL301), and Compass Therapeutics (ABL001).

Differentiator

Problem solved

Functional benefit

Brands

  • Grabody-T: 4-1BB based bispecific antibody platform for immuno-oncology that activates T cells only in tumor microenvironment
  • Grabody-B
  • Grabody-I

Products and services

  • Grabody-T Platform A 4-1BB-based bispecific antibody platform that activates T cells only in tumor microenvironments where tumor antigens are present, minimizing systemic toxicity associated with traditional 4-1BB immunotherapy. Licensed to global pharmaceutical partners as a development engine.
  • Grabody-B Platform A blood-brain barrier (BBB) shuttle platform that uses IGF1R targeting to maximize delivery of therapeutic antibodies into the brain for treatment of neurodegenerative diseases. Achieves 7x or higher BBB penetration versus monoclonal antibodies in preclinical studies.
  • Grabody-I Platform An immune checkpoint bispecific antibody platform designed to overcome limitations of conventional PD-(L)1 therapy by targeting multiple immune checkpoint pathways.
  • Givastomig (ABL111) Bispecific antibody targeting Claudin 18.2 and 4-1BB for treatment of gastric cancer, jointly developed with NovaBridge Biosciences. Received FDA Fast Track and Orphan Drug designations. Demonstrated 75% objective response rate and 16.9-month median progression-free survival in Phase 1b trial.
  • Ragistomig (ABL503) Bispecific antibody targeting PD-L1 and 4-1BB for immuno-oncology applications, designed to minimize 4-1BB toxicity while augmenting T-cell activation. Jointly developed with NovaBridge Biosciences.
  • ABL501 Bispecific antibody targeting LAG-3 and PD-L1 immune checkpoint pathways to overcome resistance and low response rates in conventional PD-(L)1 therapy.
  • ABL301 (SAR446159) Bispecific antibody for Parkinson's disease using Grabody-B platform to deliver alpha-synuclein targeting antibodies across the blood-brain barrier. Licensed to Sanofi for global development.
  • ABL001 (Tovecimig) Bispecific antibody targeting VEGF and DLL4 for treatment of solid tumors, particularly biliary tract cancer. Licensed to Compass Therapeutics.
  • ABL206 (NEOK001) First-in-class bispecific ADC targeting B7-H3 and ROR1 with topoisomerase I inhibitor payload, developed through NEOK Bio subsidiary for advanced solid tumors.
  • ABL209 (NEOK002) Bispecific ADC targeting EGFR and MUC1 with topoisomerase I inhibitor payload, developed through NEOK Bio subsidiary for advanced solid tumors.
  • ABL105 (Nesfrotamig) Bispecific antibody targeting HER2 and 4-1BB for solid tumor treatment, licensed to Yuhan Corporation for Korea and Australia development.
  • ABL103 Bispecific antibody targeting B7-H4 and 4-1BB for solid cancer treatment, designed to activate T cells only in B7-H4 expressing tumor microenvironments.
  • ABL202 (CS5001/LCB71) ROR1-targeting ADC developed in partnership with LegoChem Biosciences and licensed to CStone Pharmaceuticals for global development excluding Korea.

Quantifiable outcome

  • 75% objective response rate (ORR) and 16.9-month median progression-free survival for givastomig (ABL111) in Phase 1b trial
  • +5 more outcomes

Companies that use ABL Bio

Customer profile

Named customers8 records

Segments4 records

Ideal customer profiles2 records

ABL Bio technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

ABL Bio partnerships and signals

Strategic signal

Partnerships

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

  • Eli LillyflagshipStrategic or Co-development Partner · 26 December 2025Licensing, research, and collaboration agreement for Grabody platform worth $2.6 billion total. ABL Bio received $40 million upfront payment and $15 million equity investment from Lilly. The agreement aims to advance the Grabody platform for therapeutic development in areas including obesity and muscle disorders.
  • NeoK BiocoreStrategic or Co-development Partner · 1 November 2025ABL Bio's US subsidiary developing bispecific ADCs ABL206 (NEOK001) and ABL209 (NEOK002). Launched with $75M Series A financing led by ABL Bio. Phase 1 clinical trials initiated.
  • GSKflagshipStrategic or Co-development Partner · 1 April 2025$2.5 billion licensing agreement for development of therapies for neurodegenerative diseases using Grabody platform.
  • MSD (Merck)minorStrategic or Co-development Partner · 1 July 2024Clinical trial collaboration and supply agreement for ABL103 with KEYTRUDA (pembrolizumab) combination therapy in advanced/metastatic solid tumors.
  • SynaffixcoreTechnology or Integration · 1 January 2024Linker-payload technology licensing agreement for next-generation bispecific ADC development.
  • IntoCellcoreTechnology or Integration · 1 January 2024Linker-payload technology partnership for bispecific ADC development.
  • Ionis PharmaceuticalscoreStrategic or Co-development Partner · 15 May 2022Collaboration on siRNA and Grabody-B conjugation demonstrating delivery to cerebellum and various brain regions, muscle, heart, and lungs. Research presented at TIDES USA 2026.
  • SanofiflagshipStrategic or Co-development Partner · 1 January 2022$1.06 billion co-development and licensing agreement for ABL301 (Parkinson's disease treatment using Grabody-B platform). Includes $750M upfront payment and milestones. Sanofi responsible for Phase 2+ clinical development.
  • Yuhan CorporationcoreStrategic or Co-development Partner · 1 January 2022Licensed ABL105 (HER2x4-1BB) for development in Korea and Australia. Phase 1/2 clinical trial being conducted by Yuhan.
  • NovaBridge Biosciences (formerly I-Mab)coreStrategic or Co-development Partner · 30 March 2021Joint development of ABL111 (Givastomig) targeting Claudin 18.2 and 4-1BB for gastric cancer; ABL503 (Ragistomig) targeting PD-L1 and 4-1BB for solid tumors. FDA Fast Track designation obtained for givastomig.
  • LegoChem BiosciencescoreTechnology or Integration · 2 November 2020Expanded ADC technology cooperation including bispecific antibody ADCs. Previously successful licensing of ABL202 (LCB71) to CStone. Four joint projects ongoing including next-generation ADC development.
  • CStone PharmaceuticalscoreStrategic or Co-development Partner · 1 October 2020Licensed ABL202 (ROR1 ADC, CS5001/LCB71) for global development excluding Korea. $117M exclusive China licensing deal by TRIGR and Elpiscience included this asset.
  • Compass TherapeuticscoreStrategic or Co-development Partner · 1 January 2018Licensed ABL001 (Tovecimig) for global development excluding Korea and Greater China. Compass conducting Phase 2/3 COMPANION-002 trial in biliary tract cancer. FDA Fast Track and Orphan Drug designations obtained.

Scale indicators13 records

Recent moves6 records

Expansion highlights6 records

ABL Bio competitors and assessment

Company assessment

Direct peers

  • Xencor: Clinical-stage biotech developing engineered bispecific antibodies using the XmAb platform, with multiple pharma partnerships and pipeline assets in oncology. Comparable technology platform and licensing-based business model.
  • Macrogenics: Clinical-stage oncology biotech developing bispecific antibodies (e.g., vobramitamig duocarmazine, enoblituzumab) with multiple Big Pharma partnerships. Comparable in pipeline scope and target indications.
  • Denali Therapeutics: Biotech developing BBB-penetrant therapeutics for neurodegenerative diseases, sharing ABL Bio's Grabody-B strategic focus. Closely comparable in CNS delivery technology and target indications (Parkinson's, Alzheimer's).
  • Maverick Therapeutics (acquired by Takeda): Developed T cell-engaging bispecific antibodies using the COBRA platform. Highly comparable technology approach (conditional 4-1BB-like activation) and was acquired by Takeda in 2021, representing a potential exit path for ABL Bio.
  • Genmab: Danish biotech pioneer in bispecific antibody technology with the proprietary DuoBody platform. Most directly comparable peer in technology, business model (platform licensing), and target indications (immuno-oncology).
  • Compass Therapeutics: Clinical-stage bispecific antibody developer and ABL Bio's licensee for ABL001 (Tovecimig). Direct operating peer with overlapping pipeline in oncology and similar partnership-driven model.
  • Zymeworks: Clinical-stage biotech with the Azymetric and ZymeLink platforms for bispecific antibodies and ADCs. Direct competitor in both bispecific antibody and ADC spaces with similar licensing-driven revenue model.
  • LegoChem Biosciences: Korean biotech developing ADCs including the LCB71 (ABL202) platform that ABL Bio licensed to CStone. Direct technology partner and Korean biotech peer with overlapping ADC pipeline.
  • Harpoon Therapeutics (acquired by Merck): Developed T cell engagers and bispecific antibodies including HPN328. Acquired by Merck for $680M in 2024, providing a relevant M&A comparable for ABL Bio's platform-licensing business model.

Emerging players

  • I-Mab Biopharma / NovaBridge Biosciences: Co-development partner on ABL111 (Givastomig) and ABL503 (Ragistomig). Asian emerging biotech with comparable bispecific antibody pipeline and strategic transformation plans relevant to ABL Bio's growth model.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

ABL Bio social profiles

Digital presence

ABL Bio financial estimates

Financial estimate

Revenue estimate

Valuation estimate

ABL Bio leadership team

Management profile

Number of profiles

Profiles2 records

ABL Bio subsidiaries and ownership

Company hierarchy

Subsidiaries2 records

ABL Bio funding detail

Funding detail

Funding overview

Funding rounds5 records

Investors11 records

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

ABL Bio M&A and investment

M&A and investment

M&A

Investments2 records

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

Frequently asked questions about ABL Bio

What does ABL Bio do?

ABL Bio is a clinical-stage biotechnology company that develops proprietary bispecific antibody therapeutic platforms and pipeline candidates for immuno-oncology, neurodegenerative diseases, and antibody-drug conjugates. The company generates revenue primarily by licensing its Grabody-T, Grabody-B, and Grabody-I platforms and pipeline assets (such as ABL111, ABL503, ABL301, ABL001) to global pharmaceutical partners via upfront payments, milestone payments, and royalties.

Is ABL Bio a public or private company?

ABL Bio is a public company. It is classified as public and is currently operating.

When was ABL Bio founded?

ABL Bio was founded in 2016. It employs 51 to 100 people.

Where is ABL Bio based?

ABL Bio is headquartered in Seongnam, South Korea, in the Asia region.

How does ABL Bio make money?

Three revenue lines are on record. Technology Licensing is the primary driver. The others are milestone Payments and royalty Revenue.

Who are ABL Bio's main competitors?

Direct peers on record are Xencor, Macrogenics, Denali Therapeutics, Maverick Therapeutics (acquired by Takeda), Genmab, Compass Therapeutics, Zymeworks, LegoChem Biosciences and Harpoon Therapeutics (acquired by Merck). I-Mab Biopharma / NovaBridge Biosciences is listed as an emerging player.

Does ABL Bio have an API?

No public API is recorded for ABL Bio.

What industry is ABL Bio in?

ABL Bio's product category is Bispecific Antibody Therapeutics & Platform Licensing. Its primary akta.pro industry code is HLAIALAH, Regulatory Strategy & IND/NDA/BLA Submissions Support, with a secondary code of HLAGACAK, Clinical Trial Pharmacy & IMP Management at Site. Its NAICS code is 541714 and its SIC code is 2834.

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BusinesskoreaKOSDAQ Pharma Stocks Plunge 10.5% in One Month, Worst Among Major SectorsKOSDAQ pharmaceutical stocks fell 10.51% in a month, the worst among major sectors, as funds shifted to AI and semiconductors. The sector's year-to-date decline widened to 36.65%, with Orum Therapeutics and ABL Bio among the worst performers. Analysts expect investors to become more selective, citing a postponed promotion and relegation system.NateAbl Bio, shareholder letter regarding undisclosed information allegations... 'Strengthening internal controls and information management': Nate NewsABL Bio posted a shareholder letter stating it will cooperate with authorities investigating alleged stock trading using undisclosed information. The company will review its internal control and information management systems, and it will continue its new drug R&D and global business development as planned.NateAbl Bio's stock plummets due to a search and seizure: Nate NewsA joint response team from the Financial Services Commission, Financial Supervisory Service, and Korea Exchange launched a forced investigation into ABL Bio and its executives. The probe targets alleged profits from undisclosed information about a major technology transfer contract with a global pharmaceutical company.HeraldcorpABL Bio partner Systimmune reports 100% complete remission in lymphoma drug combo trialSystimmune, a partner of ABL Bio, reported 100% complete remission and objective response rate in a Phase 1b trial of its ADC candidate CS5001 with R-CHOP in first-line DLBCL. The trial enrolled 31 patients across doses 40-90 mcg/kg, and the company paused the trial for dose optimization. ABL Bio is advancing 10 global clinical programs.Asiae[BIO USA] ABL Bio CEO Sanghoon Lee: "Phase 3 Gastric Cancer Drug Trial to Begin This Year"ABL Bio CEO Sanghoon Lee announced at BIO USA in San Diego that the company plans to begin Phase 3 clinical trials for its gastric cancer drug Zivastomig (ABL111) by December this year, with negotiations currently underway with Novabridge for budget and preparations including substance manufacturing and clinical site selection. The bispecific antibody drug, which targets CLDN18.2 and 4-1BB as a first-line gastric cancer therapy, has received FDA Fast Track designation and CEO Lee estimates its commercial value at approximately $2.5 billion (KRW 3.4 trillion). The company is also developing its U.S. subsidiary NeocBio as a forward base for global growth, with plans to complete Phase 2 trials within five years and potentially pursue Series B investment or a Nasdaq listing.Nate첫 '코리아 라이징' 세션…K-바이오 혁신 인정받지만 "숙제는 자본"[바이오 USA] : 네이트 뉴스The first official "Korea Rising" session dedicated solely to the Korean bio industry was held at the 2026 BIO USA convention in San Diego, marking a recognition of K-bio's elevated global standing. Panelists from Samsung Biologics, ABL Bio, Il-dong Pharmaceutical, and Boehringer Ingelheim highlighted Korea's competitive strengths in innovation technology and infrastructure, with Samsung Biologics noting it builds production facilities approximately 40% faster than the industry average. The panelists commonly identified insufficient capital compared to China as the most significant challenge for Korea to achieve further advancement beyond technology exports toward large-scale technology transfers, co-development, and M&A-driven global competitiveness.MkABL Bio’s givastomig wins FDA Fast Track designationABL Bio announced that its bispecific immuno-oncology candidate givastomig (ABL111) has received Fast Track designation from the U.S. FDA for first-line treatment of Claudin 18.2-positive, HER2-negative advanced or metastatic gastric cancer. The drug, jointly developed with NovaRock Biotherapeutics, demonstrated encouraging anti-tumor activity and favorable safety in Phase 1b trials, positioning it for a registrational Phase 3 study in Q4. The partners plan to present full Phase 1b results at a global medical conference in H2 and explore potential accelerated approval pathways.The Korea HeraldABL Bio secures FDA Fast Track for gastric cancer therapyABL Bio announced that the US Food and Drug Administration granted Fast Track designation to Givastomig (ABL111), a gastric cancer treatment candidate jointly developed with NovaRock Biotherapeutics. Givastomig is a bispecific antibody targeting Claudin 18.2 and 4-1BB for patients with Claudin 18.2-positive, HER2-negative advanced or metastatic gastric cancer. Phase 1b data demonstrated encouraging efficacy and safety, with a Phase 2 trial ongoing and a Phase 3 trial scheduled to begin in Q4, and the company has already discussed a potential accelerated approval pathway with the FDA.Investing.comFDA grants fast track status to NovaBridge’s givastomig By Investing.comThe FDA granted Fast Track Designation to NovaBridge Biosciences' givastomig in combination with nivolumab and chemotherapy for treating patients with previously untreated HER2-negative advanced or metastatic gastroesophageal adenocarcinomas whose tumors are both Claudin 18.2 and PD-L1 positive. Givastomig is a CLDN18.2 x 4-1BB bispecific antibody being jointly developed through a global partnership with ABL Bio. The company expects to begin a registrational Phase 3 trial as early as the fourth quarter of 2026.BioSpaceNovaBridge Biosciences Receives FDA Fast Track Designation for Givastomig in First-Line HER2-Negative Metastatic Gastric CancerNovaBridge Biosciences announced the FDA granted Fast Track Designation to givastomig, a CLDN18.2 x 4-1BB bispecific antibody, for first-line HER2-negative metastatic gastric cancer. The designation follows Phase 1b data showing deep and durable responses. A registrational Phase 3 trial is expected to begin as early as Q4 2026.