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Acepodia

Full company profile

uuid0000myk

Namestring
Acepodia
Legal namestring
Acepodia Inc.
Websiteurl
acepodia.com
Company typeenum
Public
Founded yearint
2017
Descriptiontext

Acepodia is a clinical-stage biotechnology company developing off-the-shelf cell therapies and antibody-drug conjugates using two proprietary conjugation platforms. The Antibody-Cell Conjugation (ACC) platform, derived from Nobel Laureate Carolyn Bertozzi's bioorthogonal click chemistry, attaches tumor-targeting antibodies directly to allogeneic gamma delta 2 (γδ2) T cells and off-the-shelf NK (oNK) cells, creating potent immune cell engagers without genetic engineering. The Antibody-Dual-Drugs Conjugation (AD2C) platform enables site-selective conjugation of multiple linker-payload types to address tumor heterogeneity in ADC development. The company was spun out of UC Berkeley's Bertozzi lab in 2017 by Sonny Hsiao (the inventor of ACC technology) and former Juno/Genentech executive Patrick Yang, and is headquartered in Alameda, California with operational headquarters in Taipei, Taiwan. Acepodia listed on the Taipei Exchange in August 2023 (TPEx: 6976) and has raised approximately $260 million cumulatively, with both Series C ($109M, December 2021) and Series D ($100M, June 2023) led by Digital Mobile Venture.

The company's lead clinical programs are ACE1831, an anti-CD20 γδ2 T cell therapy in Phase 1 for non-Hodgkin's lymphoma and now also in Phase 1/2 for IgG4-Related Disease under a Pfizer Ignite collaboration, and ACE2016, an anti-EGFR γδ2 T cell therapy in Phase 1 for solid tumors with regulatory clearances in the US, Taiwan, and China. Earlier-stage programs include a GPC3-targeting AD2C candidate for hepatocellular carcinoma in preclinical development and a bispecific ADC partnership with Biocytogen combining RenLite and AD2C technologies. Acepodia has IND clearances from the FDA, TFDA, PMDA, and NMPA, indicating a deliberate multi-country APAC-plus-US regulatory strategy, and operates a ~1,650 sqm GMP cell therapy manufacturing facility in Nangang, Taipei that opened in February 2024.

Acepodia operates a hybrid business model combining proprietary clinical development with platform licensing and co-development partnerships. The company is pre-revenue and expects future revenue from one-time licensing payments, milestones, and royalties from deals such as Pfizer Ignite and Biocytogen, with longer-term cell therapy product sales upon regulatory approval. Customer segments include oncology patients with hematologic malignancies and solid tumors, autoimmune disease patients (initially IgG4-RD), and pharmaceutical partners seeking access to the ACC and AD2C platforms.

Short descriptiontext

Acepodia is a clinical-stage biotech developing off-the-shelf cell therapies and dual-payload ADCs using proprietary antibody-conjugation platforms (ACC and AD2C) derived from Nobel Laureate Carolyn Bertozzi's bioorthogonal chemistry, serving oncology and autoimmune disease patients through multi-country clinical trials in the US and APAC.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
51–100
akta.pro rankint
HeadquartersAlameda, United States
HQ citystring
Alameda
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices3 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
allogeneic cell therapy, antibody drug conjugates, cancer immunotherapy, clinical stage biotech, biopharmaceutical development
Industry3 codes
1Cell Therapy Developers (Allogeneic/Off-the-shelf)
CodeHLAAABABPrimaryYes
2Antibody-Drug Conjugates (ADCs) & Antibody Conjugates
CodeHLAAAAAEPrimaryNo
3Rare Immunology, Autoimmune & Autoinflammatory Therapies
CodeHLAIAIAEPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
SIC code1 code
  • Biological Products, (No Disgnostic Substances)2836
Product category
Cancer Cell Therapy
Social media profiles2 records
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Cell Therapy Product Sales
TypeOne Time License
Description

Acepodia is developing allogeneic off-the-shelf cell therapies (ACE1831, ACE2016) targeting hematologic cancers and solid tumors, with plans to commercialize upon regulatory approval. The company also has plans to expand into autoimmune diseases (IgG4-RD).

acepodia.com
2Platform Licensing and Co-development
TypeLicensing Royalties
Description

The company pursues licensing deals, co-development partnerships, and technology transfer agreements with pharmaceutical partners. Examples include Pfizer Ignite collaboration and Biocytogen partnership for bispecific ADCs. Partners may pay upfront fees, milestone payments, and royalties on future sales.

businesswireindia.com
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components5 values
Technology or R&D, Personnel, Operations, Marketing or Sales, Others
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 4 records shown
1ACC™
Description

Antibody-Cell Conjugation platform technology that links tumor-targeting antibodies to immune cells using bioorthogonal click chemistry, derived from Nobel Laureate Carolyn Bertozzi's research.

acepodia.com
+3 more records
Core offering1 text field

Acepodia develops and licenses first-in-class allogeneic off-the-shelf cell therapies for oncology and autoimmune diseases, built on two proprietary platforms: Antibody-Cell Conjugation (ACC) and Antibody-Dual-Drugs Conjugation (AD2C). Its clinical pipeline includes ACE1831 (CD20-targeting for non-Hodgkin's lymphoma and IgG4-Related Disease) and ACE2016 (EGFR-targeting for solid tumors), with revenue currently generated through platform licensing and co-development agreements with global pharmaceutical partners.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • ACE1831 cell manufacturing process cost is two orders of magnitude lower than current autologous CAR-T products
+2 more records
Product overview1 text field

Acepodia is a clinical-stage biotechnology company developing first-in-class cell therapies using two proprietary conjugation technology platforms: ACC™ (Antibody-Cell Conjugation) and AD2C™ (Antibody-Dual-Drugs Conjugation). The ACC platform, derived from Nobel Laureate Carolyn Bertozzi's bioorthogonal chemistry, conjugates tumor-targeting antibodies to allogeneic immune cells (γδ2 T cells and oNK cells) to create off-the-shelf cell therapies. The AD2C platform enables site-selective dual-payload antibody-drug conjugates. The lead clinical candidates are ACE1831 (CD20-targeting ACC-γδ2 T for non-Hodgkin's lymphoma and IgG4-Related Disease) and ACE2016 (EGFR-targeting ACC-γδ2 T for solid tumors). The company also has AD2C-based programs in preclinical development targeting GPC3 for hepatocellular carcinoma.

Product and service6 records
1ACC™ (Antibody-Cell Conjugation) Platform
CategoryCore Platform Technology
Description

Proprietary platform technology that uses bioorthogonal click chemistry to attach tumor-targeting antibodies directly to immune cell receptors, creating potent off-the-shelf allogeneic cell therapies without genetic engineering. Available for out-licensing and co-development with pharmaceutical partners.

2AD2C™ (Antibody-Dual-Drugs Conjugation) Platform
CategoryPlatform Technology
Description

Antibody-drug conjugate platform enabling site-selective integration of multiple linker-payload types with adjustable Drug-to-Antibody Ratio, designed to address tumor heterogeneity through dual-payload design while preserving antibody binding capacity. Licensed to partners including Biocytogen for combination with their RenLite platform.

3ACE1831
CategoryClinical Product Candidate
Description

Lead clinical candidate: CD20-targeting ACC-gamma delta 2 T cell therapy for B-cell non-Hodgkin's lymphoma and IgG4-Related Disease. Being developed in collaboration with Pfizer Ignite for the IgG4-RD indication.

4ACE2016
CategoryClinical Product Candidate
Description

EGFR-targeting ACC-gamma delta 2 T cell therapy for EGFR-expressing solid tumors. First-in-class allogeneic anti-EGFR cell therapy in Phase 1 trials.

5ACE1702
CategoryClinical Product Candidate
Description

HER2-targeting ACC-oNK cell therapy for HER2-expressing solid tumors. Previously in Phase 1 trials for advanced HER2-positive tumors; collaboration with JW Therapeutics concluded without option exercise in July 2023.

6AD2C-Oncology (GPC3)
CategoryPreclinical Product Candidate
Description

GPC3-targeting dual-payload antibody-drug conjugate developed using the AD2C platform for hepatocellular carcinoma. In preclinical development with studies planned for 2025.

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-01-08
Description

Option and license agreement enabling Acepodia to evaluate and obtain exclusive worldwide license for two bispecific antibody-drug conjugate (BsADC) programs. Biocytogen's RenLite platform is combined with Acepodia's AD2C technology for developing next-generation dual-payload bispecific ADCs (BsAD2C). In January 2026, the collaboration was expanded through an option-based evaluation framework for additional BsADC programs.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-09-04
Description

Pfizer Ignite is a biotechnology collaboration program focused on driving innovative therapies in oncology, inflammation & immunology, and other areas. Through this strategic collaboration, Pfizer provides Acepodia with resources, expertise, and support across preclinical research, clinical trial design, and regulatory strategy to accelerate the development of ACC-based cell therapies for autoimmune diseases. The collaboration specifically supports the ACE1831 IgG4-RD clinical trial with Pfizer Ignite's resources and expertise.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2023-07-12
Description

Comprehensive MOU for cell therapy co-development including clinical trial collaboration, GLP laboratory usage, manufacturing, and medical technology development. The partnership aims to advance innovative cell therapies in Taiwan.

Strategic tierMinorTypeStrategic or Co-development PartnerAnnounced on2020-07-14
Description

Option and license agreement for off-the-shelf NK cell therapies. In July 2023, JW Therapeutics announced it would not exercise its option under the agreement, as both companies mutually agreed to focus on other programs with potentially greater clinical value.

Recent move7 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Clinical-stage allogeneic CAR-T developer with off-the-shelf cell therapy pipeline across hematologic and solid tumors. Directly comparable to Acepodia's allogeneic cell therapy platform approach, though Allogene uses gene-edited αβ T cells vs. Acepodia's γδ2 T cells.

TypeDirect peer
Description

Clinical-stage biotech developing off-the-shelf allogeneic gamma delta T cell therapies for cancer and autoimmune diseases. Most direct peer to Acepodia given shared γδ T cell chassis and overlapping indications (e.g., autoimmune).

TypeDirect peer
Description

Clinical-stage iPSC-derived NK and T cell therapy developer with off-the-shelf cell therapy platform. Comparable to Acepodia's allogeneic off-the-shelf strategy and NK cell programs, with broader iPSC manufacturing capabilities.

TypeDirect peer
Description

Clinical-stage gene-edited allogeneic CAR-T developer using TALEN platform. Comparable off-the-shelf cell therapy approach with proprietary gene-editing technology stack targeting similar hematologic malignancies.

TypeDirect peer
Description

Clinical-stage iPSC-derived allogeneic cell therapy developer for hematologic and solid tumors. Comparable off-the-shelf modality and pipeline breadth, though using different cell chassis (iPSC-derived NK and T cells).

TypeDirect peer
Description

Clinical-stage allogeneic CAR-T developer using CRISPR-based gene editing. Comparable off-the-shelf cell therapy approach with oncology focus, including allogeneic CD19 CAR-T (CB-010).

TypeDirect peer
Description

Clinical-stage cell therapy company developing engineered TCR-T cell therapies for solid tumors. Comparable cell therapy modality for oncology indications, with approved Tecelra (MAGE-A4) for synovial sarcoma.

TypeBroad incumbent
Description

Commercial-stage cell therapy company with FDA-approved tumor-infiltrating lymphocyte (TIL) therapy (Amtagvi). Comparable cell therapy category leadership in oncology, though autologous rather than allogeneic platform.

TypeBroad incumbent
Description

Global pharmaceutical company with leading ADC franchise (Enhertu, Datroway). Most relevant incumbent comparator for Acepodia's AD2C ADC platform ambitions in dual-payload and next-generation ADC development.

TypeRegional player
Description

China-based clinical-stage cell therapy company developing CAR-T therapies (approved Carteyva/relmacabtagene). Regional peer with prior Acepodia partnership history (terminated HER2 oNK option in 2023), and competing Asia cell therapy presence.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

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

Segment3 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
Profiles11 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 rounds3 records

Each record includes

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

Investors8 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 →

Acepodia

Cancer Cell Therapyacepodia.com

Acepodia is a clinical-stage biotech developing off-the-shelf cell therapies and dual-payload ADCs using proprietary antibody-conjugation platforms (ACC and AD2C) derived from Nobel Laureate Carolyn Bertozzi's bioorthogonal chemistry, serving oncology and autoimmune disease patients through multi-country clinical trials in the US and APAC.

What Acepodia does

Acepodia is a clinical-stage biotechnology company developing off-the-shelf cell therapies and antibody-drug conjugates using two proprietary conjugation platforms. The Antibody-Cell Conjugation (ACC) platform, derived from Nobel Laureate Carolyn Bertozzi's bioorthogonal click chemistry, attaches tumor-targeting antibodies directly to allogeneic gamma delta 2 (γδ2) T cells and off-the-shelf NK (oNK) cells, creating potent immune cell engagers without genetic engineering. The Antibody-Dual-Drugs Conjugation (AD2C) platform enables site-selective conjugation of multiple linker-payload types to address tumor heterogeneity in ADC development. The company was spun out of UC Berkeley's Bertozzi lab in 2017 by Sonny Hsiao (the inventor of ACC technology) and former Juno/Genentech executive Patrick Yang, and is headquartered in Alameda, California with operational headquarters in Taipei, Taiwan. Acepodia listed on the Taipei Exchange in August 2023 (TPEx: 6976) and has raised approximately $260 million cumulatively, with both Series C ($109M, December 2021) and Series D ($100M, June 2023) led by Digital Mobile Venture.

The company's lead clinical programs are ACE1831, an anti-CD20 γδ2 T cell therapy in Phase 1 for non-Hodgkin's lymphoma and now also in Phase 1/2 for IgG4-Related Disease under a Pfizer Ignite collaboration, and ACE2016, an anti-EGFR γδ2 T cell therapy in Phase 1 for solid tumors with regulatory clearances in the US, Taiwan, and China. Earlier-stage programs include a GPC3-targeting AD2C candidate for hepatocellular carcinoma in preclinical development and a bispecific ADC partnership with Biocytogen combining RenLite and AD2C technologies. Acepodia has IND clearances from the FDA, TFDA, PMDA, and NMPA, indicating a deliberate multi-country APAC-plus-US regulatory strategy, and operates a ~1,650 sqm GMP cell therapy manufacturing facility in Nangang, Taipei that opened in February 2024.

Acepodia operates a hybrid business model combining proprietary clinical development with platform licensing and co-development partnerships. The company is pre-revenue and expects future revenue from one-time licensing payments, milestones, and royalties from deals such as Pfizer Ignite and Biocytogen, with longer-term cell therapy product sales upon regulatory approval. Customer segments include oncology patients with hematologic malignancies and solid tumors, autoimmune disease patients (initially IgG4-RD), and pharmaceutical partners seeking access to the ACC and AD2C platforms.

Acepodia firmographics

Firmographics
Name
Acepodia
Legal name
Acepodia Inc.
Website
https://acepodia.com
Company type
Public
Founded year
2017
Operating status
Operating
Headcount range
51–100 employees
Short description
Acepodia is a clinical-stage biotech developing off-the-shelf cell therapies and dual-payload ADCs using proprietary antibody-conjugation platforms (ACC and AD2C) derived from Nobel Laureate Carolyn Bertozzi's bioorthogonal chemistry, serving oncology and autoimmune disease patients through multi-country clinical trials in the US and APAC.
Ownership category
akta.pro rank

Acepodia industry classification

Industry
Product category
Cancer Cell Therapy
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Research and Development in Biotechnology (except Nanobiotechnology) (541714)
SIC
Biological Products, (No Disgnostic Substances) (2836)
akta.pro primary industry
Cell Therapy Developers (Allogeneic/Off-the-shelf) (HLAAABAB)
akta.pro secondary industries
Antibody-Drug Conjugates (ADCs) & Antibody Conjugates (HLAAAAAE), Rare Immunology, Autoimmune & Autoinflammatory Therapies (HLAIAIAE)

Keywords

  • Allogeneic cell therapy
  • Antibody drug conjugates
  • Cancer immunotherapy
  • Clinical stage biotech
  • Biopharmaceutical development

Where Acepodia is headquartered

Location

Headquarters

HQ city
Alameda
HQ country
United States
HQ region
North America

Offices3 records

Markets served

Acepodia 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. Cell Therapy Product Sales: Acepodia is developing allogeneic off-the-shelf cell therapies (ACE1831, ACE2016) targeting hematologic cancers and solid tumors, with plans to commercialize upon regulatory approval. The company also has plans to expand into autoimmune diseases (IgG4-RD).
  2. Platform Licensing and Co-development: The company pursues licensing deals, co-development partnerships, and technology transfer agreements with pharmaceutical partners. Examples include Pfizer Ignite collaboration and Biocytogen partnership for bispecific ADCs. Partners may pay upfront fees, milestone payments, and royalties on future sales.

Go-to-market motion1 record

Distribution channels1 record

Marketing channels6 records

Acepodia product offering

Product offering

Core offering

Acepodia develops and licenses first-in-class allogeneic off-the-shelf cell therapies for oncology and autoimmune diseases, built on two proprietary platforms: Antibody-Cell Conjugation (ACC) and Antibody-Dual-Drugs Conjugation (AD2C). Its clinical pipeline includes ACE1831 (CD20-targeting for non-Hodgkin's lymphoma and IgG4-Related Disease) and ACE2016 (EGFR-targeting for solid tumors), with revenue currently generated through platform licensing and co-development agreements with global pharmaceutical partners.

Product overview

Acepodia is a clinical-stage biotechnology company developing first-in-class cell therapies using two proprietary conjugation technology platforms: ACC™ (Antibody-Cell Conjugation) and AD2C™ (Antibody-Dual-Drugs Conjugation). The ACC platform, derived from Nobel Laureate Carolyn Bertozzi's bioorthogonal chemistry, conjugates tumor-targeting antibodies to allogeneic immune cells (γδ2 T cells and oNK cells) to create off-the-shelf cell therapies. The AD2C platform enables site-selective dual-payload antibody-drug conjugates. The lead clinical candidates are ACE1831 (CD20-targeting ACC-γδ2 T for non-Hodgkin's lymphoma and IgG4-Related Disease) and ACE2016 (EGFR-targeting ACC-γδ2 T for solid tumors). The company also has AD2C-based programs in preclinical development targeting GPC3 for hepatocellular carcinoma.

Differentiator

Problem solved

Functional benefit

Brands

  • ACC™: Antibody-Cell Conjugation platform technology that links tumor-targeting antibodies to immune cells using bioorthogonal click chemistry, derived from Nobel Laureate Carolyn Bertozzi's research.
  • AD2C™
  • ACE1831
  • ACE2016

Products and services

  • ACC™ (Antibody-Cell Conjugation) Platform Proprietary platform technology that uses bioorthogonal click chemistry to attach tumor-targeting antibodies directly to immune cell receptors, creating potent off-the-shelf allogeneic cell therapies without genetic engineering. Available for out-licensing and co-development with pharmaceutical partners.
  • AD2C™ (Antibody-Dual-Drugs Conjugation) Platform Antibody-drug conjugate platform enabling site-selective integration of multiple linker-payload types with adjustable Drug-to-Antibody Ratio, designed to address tumor heterogeneity through dual-payload design while preserving antibody binding capacity. Licensed to partners including Biocytogen for combination with their RenLite platform.
  • ACE1831 Lead clinical candidate: CD20-targeting ACC-gamma delta 2 T cell therapy for B-cell non-Hodgkin's lymphoma and IgG4-Related Disease. Being developed in collaboration with Pfizer Ignite for the IgG4-RD indication.
  • ACE2016 EGFR-targeting ACC-gamma delta 2 T cell therapy for EGFR-expressing solid tumors. First-in-class allogeneic anti-EGFR cell therapy in Phase 1 trials.
  • ACE1702 HER2-targeting ACC-oNK cell therapy for HER2-expressing solid tumors. Previously in Phase 1 trials for advanced HER2-positive tumors; collaboration with JW Therapeutics concluded without option exercise in July 2023.
  • AD2C-Oncology (GPC3) GPC3-targeting dual-payload antibody-drug conjugate developed using the AD2C platform for hepatocellular carcinoma. In preclinical development with studies planned for 2025.

Quantifiable outcome

  • ACE1831 cell manufacturing process cost is two orders of magnitude lower than current autologous CAR-T products
  • +2 more outcomes

Companies that use Acepodia

Customer profile

Named customers1 record

Segments3 records

Ideal customer profiles2 records

Acepodia technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Acepodia partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and minor.

  • Biocytogen (百奧賽圖)coreStrategic or Co-development Partner · 8 January 2025Option and license agreement enabling Acepodia to evaluate and obtain exclusive worldwide license for two bispecific antibody-drug conjugate (BsADC) programs. Biocytogen's RenLite platform is combined with Acepodia's AD2C technology for developing next-generation dual-payload bispecific ADCs (BsAD2C). In January 2026, the collaboration was expanded through an option-based evaluation framework for additional BsADC programs.
  • Pfizer (Ignite Program)coreStrategic or Co-development Partner · 4 September 2024Pfizer Ignite is a biotechnology collaboration program focused on driving innovative therapies in oncology, inflammation & immunology, and other areas. Through this strategic collaboration, Pfizer provides Acepodia with resources, expertise, and support across preclinical research, clinical trial design, and regulatory strategy to accelerate the development of ACC-based cell therapies for autoimmune diseases. The collaboration specifically supports the ACE1831 IgG4-RD clinical trial with Pfizer Ignite's resources and expertise.
  • Mackay Memorial Hospital (馬偕紀念醫院)minorStrategic or Co-development Partner · 12 July 2023Comprehensive MOU for cell therapy co-development including clinical trial collaboration, GLP laboratory usage, manufacturing, and medical technology development. The partnership aims to advance innovative cell therapies in Taiwan.
  • JW Therapeutics (藥明巨諾)minorStrategic or Co-development Partner · 14 July 2020Option and license agreement for off-the-shelf NK cell therapies. In July 2023, JW Therapeutics announced it would not exercise its option under the agreement, as both companies mutually agreed to focus on other programs with potentially greater clinical value.

Scale indicators8 records

Recent moves7 records

Expansion highlights6 records

Acepodia competitors and assessment

Company assessment

Direct peers

  • Allogene Therapeutics: Clinical-stage allogeneic CAR-T developer with off-the-shelf cell therapy pipeline across hematologic and solid tumors. Directly comparable to Acepodia's allogeneic cell therapy platform approach, though Allogene uses gene-edited αβ T cells vs. Acepodia's γδ2 T cells.
  • Adicet Bio: Clinical-stage biotech developing off-the-shelf allogeneic gamma delta T cell therapies for cancer and autoimmune diseases. Most direct peer to Acepodia given shared γδ T cell chassis and overlapping indications (e.g., autoimmune).
  • Fate Therapeutics: Clinical-stage iPSC-derived NK and T cell therapy developer with off-the-shelf cell therapy platform. Comparable to Acepodia's allogeneic off-the-shelf strategy and NK cell programs, with broader iPSC manufacturing capabilities.
  • Cellectis: Clinical-stage gene-edited allogeneic CAR-T developer using TALEN platform. Comparable off-the-shelf cell therapy approach with proprietary gene-editing technology stack targeting similar hematologic malignancies.
  • Century Therapeutics: Clinical-stage iPSC-derived allogeneic cell therapy developer for hematologic and solid tumors. Comparable off-the-shelf modality and pipeline breadth, though using different cell chassis (iPSC-derived NK and T cells).
  • Caribou Biosciences: Clinical-stage allogeneic CAR-T developer using CRISPR-based gene editing. Comparable off-the-shelf cell therapy approach with oncology focus, including allogeneic CD19 CAR-T (CB-010).
  • Adaptimmune Therapeutics: Clinical-stage cell therapy company developing engineered TCR-T cell therapies for solid tumors. Comparable cell therapy modality for oncology indications, with approved Tecelra (MAGE-A4) for synovial sarcoma.

Broad incumbents

  • Iovance Biotherapeutics: Commercial-stage cell therapy company with FDA-approved tumor-infiltrating lymphocyte (TIL) therapy (Amtagvi). Comparable cell therapy category leadership in oncology, though autologous rather than allogeneic platform.
  • Daiichi Sankyo: Global pharmaceutical company with leading ADC franchise (Enhertu, Datroway). Most relevant incumbent comparator for Acepodia's AD2C ADC platform ambitions in dual-payload and next-generation ADC development.

Regional players

  • JW Therapeutics: China-based clinical-stage cell therapy company developing CAR-T therapies (approved Carteyva/relmacabtagene). Regional peer with prior Acepodia partnership history (terminated HER2 oNK option in 2023), and competing Asia cell therapy presence.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat4 records

Key risks7 records

Key highlights7 records

Customer concentration

Acepodia social profiles

Digital presence

Acepodia financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Acepodia leadership team

Management profile

Number of profiles

Profiles11 records

Acepodia funding detail

Funding detail

Funding overview

Funding rounds3 records

Investors8 records

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

Acepodia M&A and investment

M&A and investment

M&A

Investments

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

Frequently asked questions about Acepodia

What does Acepodia do?

Acepodia develops and licenses first-in-class allogeneic off-the-shelf cell therapies for oncology and autoimmune diseases, built on two proprietary platforms: Antibody-Cell Conjugation (ACC) and Antibody-Dual-Drugs Conjugation (AD2C). Its clinical pipeline includes ACE1831 (CD20-targeting for non-Hodgkin's lymphoma and IgG4-Related Disease) and ACE2016 (EGFR-targeting for solid tumors), with revenue currently generated through platform licensing and co-development agreements with global pharmaceutical partners.

Is Acepodia a public or private company?

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

When was Acepodia founded?

Acepodia was founded in 2017. It employs 51 to 100 people.

Where is Acepodia based?

Acepodia is headquartered in Alameda, United States, in the North America region.

How does Acepodia make money?

Two revenue lines are on record. Cell Therapy Product Sales are the primary driver. The others are platform Licensing and Co-development.

Who are Acepodia's main competitors?

Direct peers on record are Allogene Therapeutics, Adicet Bio, Fate Therapeutics, Cellectis, Century Therapeutics, Caribou Biosciences and Adaptimmune Therapeutics. Broad incumbents are Iovance Biotherapeutics and Daiichi Sankyo. JW Therapeutics is listed as a regional player.

Does Acepodia have an API?

No public API is recorded for Acepodia.

What industry is Acepodia in?

Acepodia's product category is Cancer Cell Therapy. Its primary akta.pro industry code is HLAAABAB, Cell Therapy Developers (Allogeneic/Off-the-shelf), with a secondary code of HLAAAAAE, Antibody-Drug Conjugates (ADCs) & Antibody Conjugates. Its NAICS code is 325414 and its SIC code is 2836.

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Live signals
YahooAcepodia secures FDA clearance to begin Phase I ACE723 trialAcepodia received FDA clearance to begin a Phase I trial of ACE723, an antibody-drug conjugate targeting glypican-3 in patients with unresectable or metastatic hepatocellular carcinoma. The trial will assess safety, pharmacokinetics, and preliminary anti-tumour activity, with dose-escalation planned to identify a recommended dose.Clinical Trials ArenaAcepodia secures FDA clearance to begin Phase I ACE723 trialAcepodia received FDA clearance to begin a Phase I trial of ACE723, an antibody-drug conjugate targeting glypican-3 in patients with unresectable or metastatic hepatocellular carcinoma. The trial will assess safety, pharmacokinetics, and preliminary anti-tumour activity, with dose-escalation planned to identify a recommended dose.BioWorldAcepodia’s ACE-723 gains IND approval for hepatocellular carcinomaAcepodia Inc. received FDA IND clearance for ACE-723, a GPC3-targeted dual-payload antibody-drug conjugate. The company plans a phase I trial in patients with unresectable or metastatic hepatocellular carcinoma.PR Newswire APACAcepodia Announces FDA Clearance of IND Application for ACE723, a Novel Dual-Payload Antibody-Drug ConjugateAcepodia announced FDA clearance of its IND application for ACE723, a GPC3-targeted dual-payload ADC, enabling a Phase 1 trial in unresectable or metastatic hepatocellular carcinoma. The clearance advances the company's first AD2C-generated candidate into clinical development, with a dose-escalation study planned.PR NewswireAcepodia Announces FDA Clearance of IND Application for ACE723, a Novel Dual-Payload Antibody-Drug ConjugateAcepodia announced FDA clearance of its IND application for ACE723, a GPC3-targeted dual-payload ADC, enabling Phase 1 clinical development. The study will evaluate safety, pharmacokinetics, and anti-tumor activity in patients with unresectable or metastatic hepatocellular carcinoma. Acepodia also submitted an IND to China's NMPA in August 2026.MorningstarAcepodia Announces FDA Clearance of IND Application for ACE723, a Novel Dual-Payload Antibody-Drug ConjugateAcepodia received FDA clearance for its IND application for ACE723, a GPC3-targeted dual-payload antibody-drug conjugate, enabling a Phase 1 trial in unresectable or metastatic hepatocellular carcinoma. The company also submitted an IND to China's NMPA in August 2026.openPR.comIgG4-Related Disease Market Size (7MM) is Projected to grow at a CAGR of 34.60% by 2034, according to DelveInsightDelveInsight published a market report projecting the IgG4-Related Disease (IgG4-RD) market across the 7MM (United States, EU4, UK, Japan) to grow at a CAGR of 34.6% by 2034, with current market size estimated at approximately USD 182 million in 2025. Sanofi is conducting a 52-week placebo-controlled clinical study evaluating rilzabrutinib tablets for IgG4-RD flare prevention, while Acepodia Biotech Inc. announced an open-label study assessing its therapy ACE1831 in patients with the disease. The report highlights that there are currently no approved treatments specifically for IgG4-RD, though Amgen's UPLIZNA (inebilizumab) and Zenas BioPharma/Bristol Myers Squibb's obexelimab in Phase III trials represent emerging therapeutic options targeting CD19.Business Wire IndiaBiocytogen and Acepodia Expand Collaboration Through Option-based Evaluation Framework for First-in-Class Bispecific and Dual-Payload ADCs (BsAD2C)Biocytogen Pharmaceuticals and Acepodia announced an option and license agreement enabling Acepodia to evaluate and obtain an exclusive worldwide license for two bispecific antibody-drug conjugate (BsADC) programs. Under the agreement, Biocytogen is eligible to receive upfront option fees, development and regulatory milestones, and royalties on future product sales, with financial terms not disclosed. The expanded partnership combines Biocytogen's RenLite® platform with Acepodia's Antibody-Dual-Drugs Conjugation technology for the development of next-generation dual-payload bispecific ADCs.YahooPfizer (NYSE:PFE) Ends Collaboration With Acepodia And Faces Depo-Provera Legal ChallengesPfizer ended its collaboration with Acepodia and faces legal challenges over Depo-Provera. The company's stock fell 11.11% over the past year, underperforming the pharma sector, and analysts project $10.4 billion in revenue by 2028. These developments may strain investor sentiment and pressure revenue forecasts.National Center for Biotechnology InformationIndustry updates from the field of stem cell research and regenerative medicine in September 2024This article compiles various industry updates in stem cell research and regenerative medicine from September 2024, highlighting strategic collaborations such as Acepodia partnering with Pfizer Ignite and Carisma Therapeutics expanding its agreement with Moderna. It also reports on significant clinical developments, including positive trial data from BlueRock Therapeutics for a Parkinson's treatment and long-term survival results for Johnson & Johnson's CARVYKTI in multiple myeloma. Additionally, the piece covers product launches by Aurion Biotech in Japan and funding rounds for companies like GC Therapeutics and Syntax Bio.