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Abpro

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uuid00021zt

Namestring
Abpro
Legal namestring
Abpro Holdings, Inc.
Websiteurl
abpro.co
Company typeenum
Public
Founded yearint
2021
Descriptiontext

Abpro is a clinical-stage biopharmaceutical company developing next-generation bispecific and multi-specific antibody therapeutics for cancer and ophthalmologic diseases. Founded in 2007 and headquartered in Burlington, Massachusetts, the company operates two proprietary technology platforms: DiversImmune® for antibody discovery and MultiMab™ for engineering, both centered on the TetraBi tetravalent bispecific T-cell engager format. The format is designed to provide bivalent binding to tumor-associated antigens, Fc modification for reduced toxicity and extended half-life, and a symmetrical structure enabling manufacturing efficiency.

Abpro's clinical pipeline comprises four core candidates: ABP-102 (HER2 x CD3 for HER2-positive solid tumors, partnered worldwide with Celltrion, FDA IND cleared January 2026 with Phase 1 planned for H1 2026), ABP-201 (VEGF/ANG-2 for wet age-related macular degeneration and diabetic macular edema, held through majority-owned subsidiary AbMed Corporation with AstraZeneca/MedImmune licensing and Abpro Bio for Asian markets), ABP-150 (Claudin 18.2 x CD3 for gastric cancer, partnered with NJCTTQ in China and Thailand), and ABP-110 (GPC3 x CD3 for hepatocellular carcinoma, licensed from the National Cancer Institute). The company previously developed COVID-19 neutralizing antibodies ABP-300 and ABP-310.

The business model is partnership-driven rather than commercialized direct sales. Abpro is pre-revenue and generates cash primarily through upfront payments, equity investments, and development and net sales milestones from pharmaceutical partners under licensing and co-development agreements. Celltrion is the anchor partner for the lead asset with up to $1.75 billion in potential net sales milestones, and AbMed received a $30 million equity investment from Abpro Bio in 2020. Abpro became publicly traded in December 2024 via a SPAC merger with Atlantic Coastal Acquisition Corp. II but is facing Nasdaq delisting as of February 2026 due to minimum equity noncompliance, alongside governance disruptions including the March 2025 CEO departure and January 2026 board resignations.

Short descriptiontext

Abpro is a clinical-stage biopharmaceutical company developing next-generation bispecific antibody therapeutics using its proprietary DiversImmune® and MultiMab™ platforms, partnered with global pharma firms to treat cancer and ophthalmologic diseases.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersNew York, United States
HQ citystring
New York
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
bispecific antibody therapeutics, immuno-oncology drug development, antibody discovery platforms, T-cell engager therapies, biopharmaceutical pipeline development
Industry2 codes
1Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering)
CodeHLAAAIABPrimaryYes
2Bispecific & Multispecific Antibodies
CodeHLAAAAAFPrimaryNo
NAICS code2 codes
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Biological Product (except Diagnostic) Manufacturing325414
SIC code1 code
  • Biological Products, (No Disgnostic Substances)2836
Product category
Bispecific Antibody Therapeutics (Oncology and Ophthalmology Biopharmaceuticals)
Social media profiles2 records
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model2 records
1Partnership and Milestone Payments
TypeLicensing Royalties
Description

Abpro receives upfront payments, equity investments, and is eligible for development and net sales milestone payments under collaboration agreements with pharmaceutical partners. Under the Celltrion collaboration, the company received single digit million dollars upfront and is eligible for up to $1.75 billion in net sales milestones and up to $4.0 million in development milestones.

abpro.co
2Future Product Revenue
TypeOne Time License
Description

Pre-revenue clinical stage biotech company expecting to generate revenue through product sales upon regulatory approval and commercialization of pipeline candidates including ABP-102, ABP-201, ABP-150, and ABP-110

abpro.co
Marketing channels3 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

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

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1DiversImmune®
Description

Antibody discovery platform used to generate therapeutic building blocks - high affinity and high specificity antibodies with functional activity against therapeutic targets.

abpro.co
+2 more records
Core offering1 text field

Abpro is a clinical-stage biopharmaceutical company that discovers and develops next-generation bispecific and multi-specific antibody therapeutics for cancer and ophthalmologic diseases. Its pipeline candidates (ABP-102, ABP-201, ABP-150, ABP-110) are built on the proprietary DiversImmune® antibody discovery platform, MultiMab™ antibody engineering platform, and the TetraBi tetravalent bispecific T-cell engager format, and are advanced through strategic co-development and licensing partnerships with global pharmaceutical companies.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • ABP-102/CT-P72 received FDA IND clearance enabling Phase 1 trial initiation in H1 2026 for HER2+ solid tumors
+2 more records
Product overview1 text field

Abpro is a biopharmaceutical company developing next-generation antibody therapies using two proprietary technology platforms: DiversImmune® for antibody discovery and MultiMab™ for antibody engineering. The company leverages its TetraBi tetravalent bispecific antibody format for T-cell engagement. Abpro's pipeline includes four clinical-stage bispecific antibody candidates: ABP-102 (HER2/CD3 for HER2+ solid tumors, partnered with Celltrion), ABP-201 (VEGF/ANG-2 for wet AMD and diabetic macular edema, via AbMed subsidiary with AstraZeneca licensing), ABP-150 (Claudin 18.2/CD3 for gastric cancer, partnered with NJCTTQ), and ABP-110 (GPC3/CD3 for hepatocellular carcinoma, licensed from NCI). The company also developed COVID-19 antibodies (ABP-300, ABP-310) and has additional pipeline candidates including ABP 310 for COVID and ABP-201 for wet AMD.

Product and service7 records
1ABP-102 (ABP-102/CT-P72)
CategoryBispecific Antibody Therapeutic
Description

A next-generation TetraBi bispecific antibody targeting HER2 and CD3 for the treatment of HER2-positive solid tumors, including breast and gastric cancers. Features bivalent HER2 binding sites with affinity tuning to selectively target tumor cells expressing high and intermediate levels of HER2 while reducing activity on healthy tissues. Co-developed worldwide with Celltrion Inc.

2ABP-201
CategoryBispecific Antibody Therapeutic
Description

A bispecific antibody designed to simultaneously inhibit VEGF and ANG-2 for the potential treatment of vascular diseases of the eye, including diabetic macular edema (DME) and wet age-related macular degeneration (Wet AMD). Held through majority-owned subsidiary AbMed Corporation, with worldwide rights licensed from AstraZeneca/MedImmune and regional rights licensed to Abpro Bio in Asia/Middle East/CIS countries.

3ABP-150
CategoryBispecific Antibody Therapeutic
Description

A TetraBi antibody targeting Claudin 18.2 and CD3 for the potential treatment of gastric cancers. Designed to bind bivalently to Claudin 18.2 on gastric cancer cells and to CD3 on cytotoxic T cells, leading to T-cell-mediated killing of gastric tumor cells. Abpro retains worldwide commercialization rights; NJCTTQ holds exclusive rights in China and Thailand.

4ABP-110
CategoryBispecific Antibody Therapeutic
Description

A TetraBi antibody targeting GPC3 and CD3 for the potential treatment of hepatocellular carcinoma (HCC), the major form of liver cancer. Designed to bind bivalently to GPC3 on HCC cells and CD3 on cytotoxic T cells, triggering sustained T-cell activation and tumor cell killing. Licensed worldwide from the National Cancer Institute (NCI/NIH) effective August 1, 2017.

5DiversImmune® Antibody Discovery Platform
CategoryAntibody Discovery Technology Platform
Description

Proprietary antibody discovery platform used to generate therapeutic antibody building blocks—high affinity and high specificity antibodies with functional activity against therapeutic targets. Available as a technology platform underlying Abpro's pipeline and available for partnership.

6MultiMab™ Antibody Engineering Platform
CategoryAntibody Engineering Technology Platform
Description

Proprietary antibody engineering platform used to construct therapeutic product candidates by assembling antibody building blocks into different combinations of bi- and multi-specific antibodies. Underpins Abpro's TetraBi format and pipeline.

7TetraBi Antibody Format
CategoryBispecific Antibody Format / T-Cell Engager Technology
Description

A tetravalent bispecific T-cell engager antibody format offering bivalent binding to tumor-associated antigens for potentially increased efficacy, Fc modification for reducing toxicity and increasing antibody half-life, and flexible configuration for increased safety and/or maximized efficacy. Foundational technology underlying Abpro's pipeline candidates.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership5 partners
Strategic tierFlagshipTypeStrategic or Co-development PartnerAnnounced on2022-09-01
Description

Worldwide strategic partnership for development and commercialization of ABP-102/CT-P72, a bispecific HER2 x CD3 T-cell engager. Abpro received single digit million dollars upfront and equity investment, eligible for up to $1.75 billion in net sales milestones and up to $4.0 million in development milestones. Celltrion responsible for CMC, in vivo preclinical work, clinical development, and worldwide commercialization. Abpro responsible for in vitro pre-clinical work.

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

Collaboration and License Agreement for ABP-201 in Asia and Middle East. Abpro Bio granted exclusive rights in China, Japan, South Korea, Southeast Asia, Middle East, and CIS countries. AbMed received $30 million equity investment from Abpro Bio in connection with this agreement.

3Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd (NJCTTQ)
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2019-02-01
Description

Partnership for development of multiple novel bispecific antibodies including ABP-150 (Claudin 18.2 x CD3). NJCTTQ holds exclusive commercialization rights in China and Thailand; Abpro retains worldwide commercialization rights for ABP-150.

abpro.co
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2017-08-01
Description

Patent license granted by NCI for worldwide exclusive rights to ABP-110 (GPC3/CD3 bispecific antibody) for treatment of GPC-3 expressing liver cancer using particular moiety for targeting GPC3.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2016-08-01
Description

Collaboration and license agreement through majority-owned subsidiary AbMed Corporation. MedImmune/AstraZeneca granted exclusive worldwide license for ANG-2/VEGF-H1RK bispecific antibodies. Abpro holds 82% of AbMed, AstraZeneca holds remainder. Lead candidate ABP-201 targeting VEGF/ANG2 anticipated to enter Phase 1 in H2 2025.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage biotech with POWERbody and SAFEbody antibody platforms for bispecific and conditionally active antibodies. Comparable platform-licensing business model and early clinical stage to Abpro.

TypeDirect peer
Description

Clinical-stage biotech developing bispecific and multispecific antibody therapeutics using proprietary platforms (Azymetric, EFECT). Most directly comparable to Abpro in platform-based bispecific antibody discovery with multiple clinical-stage oncology candidates.

TypeDirect peer
Description

Established antibody therapeutics company with the DuoBody bispecific platform and a portfolio of clinical and commercial-stage bispecific antibodies (including approved Epkinly). Comparable technology foundation to Abpro's MultiMab and broader pipeline ambition.

TypeBroad incumbent
Description

Global biopharma and existing Abpro partner through AbMed Corporation for ANG-2/VEGF bispecifics. A relevant incumbent both as a comparison point for bispecific R&D capacity and as the partner validating Abpro's AbMed platform economics.

TypeDirect peer
Description

Developed T-cell engager bispecific antibodies (TriTAC platform) before acquisition by Merck. Closely analogous to Abpro's TetraBi T-cell engager focus and partnered-program structure prior to acquisition.

TypeDirect peer
Description

Clinical-stage biotech with DART and TRIDENT platforms for bispecific and multi-specific antibodies, including T-cell engagers. Direct competitor to Abpro's TetraBi format in HER2 and other oncology targets.

TypeDirect peer
Description

Clinical-stage biotech developing bispecific antibodies for oncology, including T-cell engagers. Comparable size and pipeline stage to Abpro with similarly platform-driven approach to multi-specific antibody development.

TypeBroad incumbent
Description

Major biopharma with approved bispecific antibodies (e.g., Linvoseltamab-class programs, Veopoz) and the VelociBi antibody platform. Represents the scaled end-state Abpro could aspire to as a platform-driven bispecific developer.

TypeDirect peer
Description

Clinical-stage biotech with the XmAb antibody engineering platform used to develop bispecific antibodies and T-cell engagers. Directly comparable to Abpro as a platform-based bispecific developer with multiple partnered programs.

TypeRegional player
Description

China-headquartered clinical-stage biopharma licensing and developing bispecific antibodies and oncology therapeutics in Asia. Comparable role to NJCTTQ/Abpro Bio as a regional commercialization partner for next-generation antibody programs in China and broader Asia.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights6 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 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
Profiles10 records

Each record includes

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

Subsidiaries1 record

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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 rounds8 records

Each record includes

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

Investors1 record

Each record includes

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

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

M&A1 record

Each record includes

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

Investment

Each record includes

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

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

Abpro

Bispecific Antibody Therapeutics (Oncology and Ophthalmology Biopharmaceuticals)abpro.co

Abpro is a clinical-stage biopharmaceutical company developing next-generation bispecific antibody therapeutics using its proprietary DiversImmune® and MultiMab™ platforms, partnered with global pharma firms to treat cancer and ophthalmologic diseases.

What Abpro does

Abpro is a clinical-stage biopharmaceutical company developing next-generation bispecific and multi-specific antibody therapeutics for cancer and ophthalmologic diseases. Founded in 2007 and headquartered in Burlington, Massachusetts, the company operates two proprietary technology platforms: DiversImmune® for antibody discovery and MultiMab™ for engineering, both centered on the TetraBi tetravalent bispecific T-cell engager format. The format is designed to provide bivalent binding to tumor-associated antigens, Fc modification for reduced toxicity and extended half-life, and a symmetrical structure enabling manufacturing efficiency.

Abpro's clinical pipeline comprises four core candidates: ABP-102 (HER2 x CD3 for HER2-positive solid tumors, partnered worldwide with Celltrion, FDA IND cleared January 2026 with Phase 1 planned for H1 2026), ABP-201 (VEGF/ANG-2 for wet age-related macular degeneration and diabetic macular edema, held through majority-owned subsidiary AbMed Corporation with AstraZeneca/MedImmune licensing and Abpro Bio for Asian markets), ABP-150 (Claudin 18.2 x CD3 for gastric cancer, partnered with NJCTTQ in China and Thailand), and ABP-110 (GPC3 x CD3 for hepatocellular carcinoma, licensed from the National Cancer Institute). The company previously developed COVID-19 neutralizing antibodies ABP-300 and ABP-310.

The business model is partnership-driven rather than commercialized direct sales. Abpro is pre-revenue and generates cash primarily through upfront payments, equity investments, and development and net sales milestones from pharmaceutical partners under licensing and co-development agreements. Celltrion is the anchor partner for the lead asset with up to $1.75 billion in potential net sales milestones, and AbMed received a $30 million equity investment from Abpro Bio in 2020. Abpro became publicly traded in December 2024 via a SPAC merger with Atlantic Coastal Acquisition Corp. II but is facing Nasdaq delisting as of February 2026 due to minimum equity noncompliance, alongside governance disruptions including the March 2025 CEO departure and January 2026 board resignations.

Abpro firmographics

Firmographics
Name
Abpro
Legal name
Abpro Holdings, Inc.
Website
https://abpro.co
Company type
Public
Founded year
2021
Operating status
Operating
Headcount range
1–10 employees
Short description
Abpro is a clinical-stage biopharmaceutical company developing next-generation bispecific antibody therapeutics using its proprietary DiversImmune® and MultiMab™ platforms, partnered with global pharma firms to treat cancer and ophthalmologic diseases.
Ownership category
akta.pro rank

Abpro industry classification

Industry
Product category
Bispecific Antibody Therapeutics (Oncology and Ophthalmology Biopharmaceuticals)
NAICS
Research and Development in Biotechnology (except Nanobiotechnology) (541714), Biological Product (except Diagnostic) Manufacturing (325414)
SIC
Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering) (HLAAAIAB)
akta.pro secondary industry
Bispecific & Multispecific Antibodies (HLAAAAAF)

Keywords

  • Bispecific antibody therapeutics
  • Immuno-oncology drug development
  • Antibody discovery platforms
  • T-cell engager therapies
  • Biopharmaceutical pipeline development

Where Abpro is headquartered

Location

Headquarters

HQ city
New York
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Abpro business model

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

Revenue model

  1. Partnership and Milestone Payments: Abpro receives upfront payments, equity investments, and is eligible for development and net sales milestone payments under collaboration agreements with pharmaceutical partners. Under the Celltrion collaboration, the company received single digit million dollars upfront and is eligible for up to $1.75 billion in net sales milestones and up to $4.0 million in development milestones.
  2. Future Product Revenue: Pre-revenue clinical stage biotech company expecting to generate revenue through product sales upon regulatory approval and commercialization of pipeline candidates including ABP-102, ABP-201, ABP-150, and ABP-110

Go-to-market motion2 records

Distribution channels4 records

Marketing channels3 records

Abpro product offering

Product offering

Core offering

Abpro is a clinical-stage biopharmaceutical company that discovers and develops next-generation bispecific and multi-specific antibody therapeutics for cancer and ophthalmologic diseases. Its pipeline candidates (ABP-102, ABP-201, ABP-150, ABP-110) are built on the proprietary DiversImmune® antibody discovery platform, MultiMab™ antibody engineering platform, and the TetraBi tetravalent bispecific T-cell engager format, and are advanced through strategic co-development and licensing partnerships with global pharmaceutical companies.

Product overview

Abpro is a biopharmaceutical company developing next-generation antibody therapies using two proprietary technology platforms: DiversImmune® for antibody discovery and MultiMab™ for antibody engineering. The company leverages its TetraBi tetravalent bispecific antibody format for T-cell engagement. Abpro's pipeline includes four clinical-stage bispecific antibody candidates: ABP-102 (HER2/CD3 for HER2+ solid tumors, partnered with Celltrion), ABP-201 (VEGF/ANG-2 for wet AMD and diabetic macular edema, via AbMed subsidiary with AstraZeneca licensing), ABP-150 (Claudin 18.2/CD3 for gastric cancer, partnered with NJCTTQ), and ABP-110 (GPC3/CD3 for hepatocellular carcinoma, licensed from NCI). The company also developed COVID-19 antibodies (ABP-300, ABP-310) and has additional pipeline candidates including ABP 310 for COVID and ABP-201 for wet AMD.

Differentiator

Problem solved

Functional benefit

Brands

  • DiversImmune®: Antibody discovery platform used to generate therapeutic building blocks - high affinity and high specificity antibodies with functional activity against therapeutic targets.
  • MultiMab™
  • TetraBi™

Products and services

  • ABP-102 (ABP-102/CT-P72) A next-generation TetraBi bispecific antibody targeting HER2 and CD3 for the treatment of HER2-positive solid tumors, including breast and gastric cancers. Features bivalent HER2 binding sites with affinity tuning to selectively target tumor cells expressing high and intermediate levels of HER2 while reducing activity on healthy tissues. Co-developed worldwide with Celltrion Inc.
  • ABP-201 A bispecific antibody designed to simultaneously inhibit VEGF and ANG-2 for the potential treatment of vascular diseases of the eye, including diabetic macular edema (DME) and wet age-related macular degeneration (Wet AMD). Held through majority-owned subsidiary AbMed Corporation, with worldwide rights licensed from AstraZeneca/MedImmune and regional rights licensed to Abpro Bio in Asia/Middle East/CIS countries.
  • ABP-150 A TetraBi antibody targeting Claudin 18.2 and CD3 for the potential treatment of gastric cancers. Designed to bind bivalently to Claudin 18.2 on gastric cancer cells and to CD3 on cytotoxic T cells, leading to T-cell-mediated killing of gastric tumor cells. Abpro retains worldwide commercialization rights; NJCTTQ holds exclusive rights in China and Thailand.
  • ABP-110 A TetraBi antibody targeting GPC3 and CD3 for the potential treatment of hepatocellular carcinoma (HCC), the major form of liver cancer. Designed to bind bivalently to GPC3 on HCC cells and CD3 on cytotoxic T cells, triggering sustained T-cell activation and tumor cell killing. Licensed worldwide from the National Cancer Institute (NCI/NIH) effective August 1, 2017.
  • DiversImmune® Antibody Discovery Platform Proprietary antibody discovery platform used to generate therapeutic antibody building blocks—high affinity and high specificity antibodies with functional activity against therapeutic targets. Available as a technology platform underlying Abpro's pipeline and available for partnership.
  • MultiMab™ Antibody Engineering Platform Proprietary antibody engineering platform used to construct therapeutic product candidates by assembling antibody building blocks into different combinations of bi- and multi-specific antibodies. Underpins Abpro's TetraBi format and pipeline.
  • TetraBi Antibody Format A tetravalent bispecific T-cell engager antibody format offering bivalent binding to tumor-associated antigens for potentially increased efficacy, Fc modification for reducing toxicity and increasing antibody half-life, and flexible configuration for increased safety and/or maximized efficacy. Foundational technology underlying Abpro's pipeline candidates.

Quantifiable outcome

  • ABP-102/CT-P72 received FDA IND clearance enabling Phase 1 trial initiation in H1 2026 for HER2+ solid tumors
  • +2 more outcomes

Companies that use Abpro

Customer profile

Segments2 records

Ideal customer profiles2 records

Abpro technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Abpro partnerships and signals

Strategic signal

Partnerships

Five partnerships are on record, tiered flagship and core.

  • Celltrion Inc.flagshipStrategic or Co-development Partner · 1 September 2022Worldwide strategic partnership for development and commercialization of ABP-102/CT-P72, a bispecific HER2 x CD3 T-cell engager. Abpro received single digit million dollars upfront and equity investment, eligible for up to $1.75 billion in net sales milestones and up to $4.0 million in development milestones. Celltrion responsible for CMC, in vivo preclinical work, clinical development, and worldwide commercialization. Abpro responsible for in vitro pre-clinical work.
  • Abpro Bio International (Abpro Bio Co. Ltd)coreStrategic or Co-development Partner · 1 January 2020Collaboration and License Agreement for ABP-201 in Asia and Middle East. Abpro Bio granted exclusive rights in China, Japan, South Korea, Southeast Asia, Middle East, and CIS countries. AbMed received $30 million equity investment from Abpro Bio in connection with this agreement.
  • Nanjing Chia Tai Tianqing Pharmaceutical Co., Ltd (NJCTTQ)coreStrategic or Co-development Partner · 1 February 2019Partnership for development of multiple novel bispecific antibodies including ABP-150 (Claudin 18.2 x CD3). NJCTTQ holds exclusive commercialization rights in China and Thailand; Abpro retains worldwide commercialization rights for ABP-150.
  • National Cancer Institute (NCI/NIH)coreStrategic or Co-development Partner · 1 August 2017Patent license granted by NCI for worldwide exclusive rights to ABP-110 (GPC3/CD3 bispecific antibody) for treatment of GPC-3 expressing liver cancer using particular moiety for targeting GPC3.
  • AstraZeneca (formerly MedImmune)coreStrategic or Co-development Partner · 1 August 2016Collaboration and license agreement through majority-owned subsidiary AbMed Corporation. MedImmune/AstraZeneca granted exclusive worldwide license for ANG-2/VEGF-H1RK bispecific antibodies. Abpro holds 82% of AbMed, AstraZeneca holds remainder. Lead candidate ABP-201 targeting VEGF/ANG2 anticipated to enter Phase 1 in H2 2025.

Scale indicators4 records

Recent moves7 records

Expansion highlights4 records

Abpro competitors and assessment

Company assessment

Direct peers

  • Adagene: Clinical-stage biotech with POWERbody and SAFEbody antibody platforms for bispecific and conditionally active antibodies. Comparable platform-licensing business model and early clinical stage to Abpro.
  • Zymeworks: Clinical-stage biotech developing bispecific and multispecific antibody therapeutics using proprietary platforms (Azymetric, EFECT). Most directly comparable to Abpro in platform-based bispecific antibody discovery with multiple clinical-stage oncology candidates.
  • Genmab: Established antibody therapeutics company with the DuoBody bispecific platform and a portfolio of clinical and commercial-stage bispecific antibodies (including approved Epkinly). Comparable technology foundation to Abpro's MultiMab and broader pipeline ambition.
  • Harpoon Therapeutics: Developed T-cell engager bispecific antibodies (TriTAC platform) before acquisition by Merck. Closely analogous to Abpro's TetraBi T-cell engager focus and partnered-program structure prior to acquisition.
  • MacroGenics: Clinical-stage biotech with DART and TRIDENT platforms for bispecific and multi-specific antibodies, including T-cell engagers. Direct competitor to Abpro's TetraBi format in HER2 and other oncology targets.
  • Compass Therapeutics: Clinical-stage biotech developing bispecific antibodies for oncology, including T-cell engagers. Comparable size and pipeline stage to Abpro with similarly platform-driven approach to multi-specific antibody development.
  • Xencor: Clinical-stage biotech with the XmAb antibody engineering platform used to develop bispecific antibodies and T-cell engagers. Directly comparable to Abpro as a platform-based bispecific developer with multiple partnered programs.

Broad incumbents

  • AstraZeneca: Global biopharma and existing Abpro partner through AbMed Corporation for ANG-2/VEGF bispecifics. A relevant incumbent both as a comparison point for bispecific R&D capacity and as the partner validating Abpro's AbMed platform economics.
  • Regeneron Pharmaceuticals: Major biopharma with approved bispecific antibodies (e.g., Linvoseltamab-class programs, Veopoz) and the VelociBi antibody platform. Represents the scaled end-state Abpro could aspire to as a platform-driven bispecific developer.

Regional players

  • Zai Lab: China-headquartered clinical-stage biopharma licensing and developing bispecific antibodies and oncology therapeutics in Asia. Comparable role to NJCTTQ/Abpro Bio as a regional commercialization partner for next-generation antibody programs in China and broader Asia.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat3 records

Key risks6 records

Key highlights6 records

Customer concentration

Abpro social profiles

Digital presence

Abpro financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Abpro leadership team

Management profile

Number of profiles

Profiles10 records

Abpro subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Abpro funding detail

Funding detail

Funding overview

Funding rounds8 records

Investors1 record

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

Abpro M&A and investment

M&A and investment

M&A1 record

Investments

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

Frequently asked questions about Abpro

What does Abpro do?

Abpro is a clinical-stage biopharmaceutical company that discovers and develops next-generation bispecific and multi-specific antibody therapeutics for cancer and ophthalmologic diseases. Its pipeline candidates (ABP-102, ABP-201, ABP-150, ABP-110) are built on the proprietary DiversImmune® antibody discovery platform, MultiMab™ antibody engineering platform, and the TetraBi tetravalent bispecific T-cell engager format, and are advanced through strategic co-development and licensing partnerships with global pharmaceutical companies.

Is Abpro a public or private company?

Abpro is a public company. It is classified as public and is currently operating.

When was Abpro founded?

Abpro was founded in 2021. It employs 1 to 10 people.

Where is Abpro based?

Abpro is headquartered in New York, United States, in the North America region.

How does Abpro make money?

Two revenue lines are on record. Partnership and Milestone Payments are the primary driver. The others are future Product Revenue.

Who are Abpro's main competitors?

Direct peers on record are Adagene, Zymeworks, Genmab, Harpoon Therapeutics, MacroGenics, Compass Therapeutics and Xencor. Broad incumbents are AstraZeneca and Regeneron Pharmaceuticals. Zai Lab is listed as a regional player.

Does Abpro have an API?

No public API is recorded for Abpro.

What industry is Abpro in?

Abpro's product category is Bispecific Antibody Therapeutics (Oncology and Ophthalmology Biopharmaceuticals). Its primary akta.pro industry code is HLAAAIAB, Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering), with a secondary code of HLAAAAAF, Bispecific & Multispecific Antibodies. Its NAICS code is 541714 and its SIC code is 2836.

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Investing.comAbpro Holdings to be delisted from Nasdaq after failing equity requirement By Investing.comAbpro Holdings received notice from the Nasdaq Hearings Panel that its securities will be delisted from the Nasdaq Stock Market after failing to meet the minimum equity standard required under Nasdaq Listing Rule 5550(b)(1) by February 16, 2026. Trading of the company's common stock and warrants is scheduled to be suspended at the open of trading on Monday, February 23, with the company stating it intends to appeal the Panel's decision within the 15-day window. The delisting follows governance challenges including resignations of board members that left the board without a majority of independent directors and the audit committee short of required independent members, resulting in Nasdaq noncompliance notices.Investing.comABPRO stock tumbles on Nasdaq listing compliance issues By Investing.comABPRO's stock declined 9.4% in premarket trading after Nasdaq sent notices regarding its failure to meet multiple listing requirements, including board independence and audit committee composition. The company has initiated efforts to address these deficiencies but faces the risk of delisting if it cannot regain compliance.Investing.comABPRO stock tumbles on Nasdaq listing compliance issues By Investing.comABPRO's stock fell 9.4% in premarket trading after the biotechnology company disclosed it received Nasdaq notices regarding failures to meet listing requirements, following the January resignations of two board members, Anthony D. Eisenberg and Sooyoung Lee. The company is no longer in compliance with Nasdaq rules requiring a majority of independent directors on its board and at least three independent audit committee members, with formal notification received on February 5 that these failures constitute additional bases for delisting. ABPRO has initiated a process to appoint qualified independent directors but acknowledged there is no assurance the Nasdaq Hearings Panel will grant continued listing.Investing.comABPRO stock tumbles on Nasdaq listing compliance issues By Investing.comABPRO's stock fell 9.4% in premarket trading after it received notices from Nasdaq regarding its failure to meet multiple listing requirements following the resignation of two board members. The company disclosed deficiencies related to its board independence and audit committee, with Nasdaq indicating potential delisting if compliance was not restored.Investing.comAbpro Holdings receives Nasdaq noncompliance notice, appoints new board members By Investing.comAbpro Holdings received notices from Nasdaq indicating non-compliance with listing requirements following the resignations of two board members, Anthony D. Eisenberg and Sooyoung Lee, which left the board without a majority of independent directors and the audit committee with fewer than three members as required by Nasdaq Listing Rules. The company appointed M. Fatih Karatas and Mary Gunn to fill the vacancies and must submit its response to the Nasdaq Hearings Panel by February 12, with a compliance deadline of early 2027. Separately, the FDA cleared Abpro's Investigational New Drug application for ABP-102/CT-P72, a multispecific antibody oncology program co-developed with Celltrion, allowing Phase 1 clinical trials for HER2-positive solid tumors to begin in H1 2026.Benzinga12 Health Care Stocks Moving In Wednesday's Pre-Market Session - Aditxt Inc Ordinary Shares (NASDAQ:ADTX)A Benzinga market data article reported pre-market price movements for 12 healthcare stocks on Wednesday, with six gainers and six losers. The largest gainer was Anteris Technologies (AVR), up 20.7% to $6.94 with a $236.8 million market cap, while the largest loser was AlphaTON Capital (ATON), down 18.7% to $0.75. The remaining movers ranged from gainers including Aditxt (+20.33%), Abpro Holdings (+13.26%), Matinas BioPharma (+8.86%), Tevogen Bio (+8.45%), and Akari Therapeutics (+8.22%), to losers including INVO Fertility (-15.62%), GlucoTrack (-14.22%), Shuttle Pharmaceuticals (-11.22%), Propanc Biopharma (-9.18%), and Alzamend Neuro (-9.1%).Investing.comAbpro stock rises after FDA clearance for solid tumor program By Investing.comAbpro's stock rose 5.2% in premarket trading after the FDA cleared its Investigational New Drug application for ABP-102/CT-P72, a multispecific antibody oncology program targeting HER2-positive solid tumors. The clearance enables Abpro and co-development partner Celltrion to begin a Phase 1 clinical trial evaluating the drug candidate's safety and preliminary efficacy, marking Abpro's first clinical-stage T-cell engager program in oncology. The companies plan to initiate a global Phase 1 trial in the first half of 2026, following positive preclinical results showing antitumor activity and good tolerability in toxicology studies.GlobeNewswireAbpro Granted Nasdaq Listing Extension to Pursue Compliance and Strategic ObjectivesAbpro Holdings, Inc. has received an extension from the Nasdaq Hearings Panel to regain compliance with listing requirements, having completed a reverse stock split on November 3 as part of its compliance roadmap. The company has achieved an estimated 60% reduction in operating expenses and has access to up to $44 million in equity financing to fund operations through 2026. Abpro's lead antibody candidate ABP-102, developed in partnership with Celltrion, remains on track for first-in-human trials in 2026.GlobeNewswireAbpro and Celltrion to Present Preclinical Data for CT-P72/ABP-102 at SITC 2025, Highlighting a Next-Generation HER2×CD3 T-Cell EngagerAbpro Corporation and Celltrion announced they will present preclinical data for CT-P72/ABP-102, a HER2×CD3 bispecific T-cell engager, at SITC 2025, with their abstract selected as one of the Top 150 out of over 1,300 submissions. The drug demonstrated potent anti-tumor activity in HER2-high models including Enhertu-resistant tumors, while maintaining a favorable safety profile in non-human primates. The companies are working toward an IND submission and first-in-human trial next year for HER2-positive solid tumors.GlobeNewswireAbpro Announces 1-for-30 Reverse Stock Split Effective November 3, 2025Abpro Holdings, Inc. announced the effectiveness of its 1-for-30 reverse stock split at 5:01 p.m. Eastern Time on October 31, 2025, reducing its outstanding shares from approximately 81.2 million to 2.7 million, with trading on a split-adjusted basis beginning November 3, 2025. The company stated the split is designed to help maintain compliance with Nasdaq minimum bid price requirements, citing an estimated 60% reduction in operating costs versus the same period in 2024. Abpro highlighted its partnership with Celltrion, which funds all development expenses for its lead antibody program ABP-102, with a first-in-human trial anticipated in 2026.