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Immunwork

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uuid000328x

Namestring
Immunwork
Legal namestring
免疫功坊股份有限公司 (Immunwork, Inc.)
Websiteurl
immunwork.com
Company typeenum
Private
Founded yearint
2014
Descriptiontext

Immunwork, Inc. (免疫功坊股份有限公司) is a clinical-stage biotechnology company founded in October 2014 in Taipei, Taiwan, operating as a wholly owned subsidiary of Cayman Islands-incorporated T-E Pharma Holding. The company develops ultra-long-acting drug candidates for endocrine, metabolic, and cardiovascular diseases using its proprietary T-E pharmaceutical technology platform, which combines targeting (T) and effector (E) moieties through novel multi-arm linkers. Its lead technology, the Fatty Acid Bundle platform, conjugates 2-3 fatty acid molecules to therapeutic peptides to enhance serum albumin binding and extend circulation half-life, with sister company T-E Meds (established 2022) extending the platform into antibody-drug conjugates (ADCs) and antibody-radionuclide conjugates (ARCs) for oncology applications.

The company's clinical pipeline includes TE-8105, a long-acting GLP-1 receptor agonist for type 2 diabetes and obesity that completed Phase 1/2a trials in Australia in 2025; TE-8214, a long-acting octreotide analog for acromegaly and neuroendocrine tumors that completed Phase I in 2025; TE-6168, a thrombolytic fusion protein for ischemic stroke and myocardial infarction; and TE-1146, an ADC for multiple myeloma licensed to Orient EuroPharma. The company has raised approximately USD 45 million across Immunwork funding rounds (2021 Series A and 2022 A-round) plus USD 26 million for T-E Meds, and collected an USD 8.5 million upfront licensing payment from Orient EuroPharma in January 2025.

Immunwork's revenue model is entirely licensing- and partnership-driven, with no commercialized products. The company generates revenue through upfront licensing fees, development milestones, and royalties upon partner commercialization, supported by a partnership ecosystem that includes Orient EuroPharma (commercial licensee for TE-1146), Asymchem Laboratories (CDMO and CRO services), CHO Pharma (CHO-TEM joint technology), and prospective global pharmaceutical partners accessed via industry conferences including BIO Asia-Taiwan, the J.P. Morgan Healthcare Conference, and World ADC conferences. The parent T-E Pharma Holding is targeting a TPEx Emerging Stock Board listing in Q4 2026 to provide a public capital exit while retaining the holding structure.

Short descriptiontext

Immunwork is a clinical-stage Taiwanese biotech developing ultra-long-acting therapeutics for metabolic, endocrine, and cardiovascular diseases using its proprietary multi-arm linker and fatty acid bundle platforms, operating alongside sister company T-E Meds under T-E Pharma Holding.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
11–50
akta.pro rankint
HeadquartersTaipei, Taiwan
HQ citystring
Taipei
HQ countrystring
Taiwan
HQ regionstring
Asia
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
ultra-long-acting peptides, antibody-drug conjugates, fatty acid bundle platform, multi-arm linker technology, clinical-stage biopharmaceuticals
Industry3 codes
1Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering)
CodeHLAAAIABPrimaryYes
2Antibody-Drug Conjugates (ADCs) & Antibody Conjugates
CodeHLAAAAAEPrimaryNo
3Endocrinology & Reproductive Health Pharmaceuticals (incl. Women’s Health)
CodeHLAIAAAJPrimaryNo
NAICS code3 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Research and Development in Biotechnology (except Nanobiotechnology)541714
  • Pharmaceutical Preparation Manufacturing325412
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Biopharmaceuticals
Social media profiles1 record
GTM motion3 records

Each record includes

Type, Description, Source

Revenue model3 records
1Drug Development and Licensing
TypeLicensing Royalties
Description

Pre-revenue clinical-stage biotech company. Revenue expected from out-licensing of drug candidates, milestone payments, and royalties from commercialization. TE-1146 licensing to Orient EuroPharma generated USD 8.5 million upfront.

immunwork.com
2Strategic Partnerships and Collaborations
TypeLicensing Royalties
Description

Co-development arrangements with pharmaceutical partners for T-E product candidates, potentially generating upfront fees, development milestones, and commercialization revenues.

immunwork.com
3Platform Technology Licensing
TypeLicensing Royalties
Description

Licensing of multi-arm linker platforms to design new drugs for various disease indications, generating technology access fees and ongoing collaboration payments.

immunwork.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

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

Cost components4 values
Personnel, Technology or R&D, Operations, Marketing or Sales
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Core offering1 text field

Immunwork is a clinical-stage biotechnology company developing ultra-long-acting drug candidates using its proprietary T-E (targeting and effector) pharmaceutical platform. The company leverages fatty acid bundle technology to create drug candidates with extended half-lives for metabolic diseases (diabetes, obesity), endocrine disorders (acromegaly, neuroendocrine tumors), and cardiovascular conditions (thrombolytic therapy). Its sister company T-E Meds extends the platform to antibody-drug conjugates (ADCs) and antibody-radionuclide conjugates (ARCs) for oncology indications.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • TE-8105 demonstrated half-life of 15 hours in mice, approximately 2x that of semaglutide (7.5 hours)
+5 more records
Product and service5 records
1TE-8105
CategoryMetabolic Disease Therapeutics
Description

TE-8105 is a long-acting GLP-1 receptor agonist developed using the fatty acid bundle platform for the treatment of type 2 diabetes, obesity, and non-alcoholic fatty liver disease (NAFLD/NASH). It demonstrated a half-life of 15 hours in mice versus 7.5 hours for semaglutide, enabling potential once-every-two-weeks dosing with superior glucose control and weight loss in preclinical models. Phase 1/2a results showed 5 of 8 participants in B2 cohort achieved >5% body weight reduction.

2TE-8214
CategoryEndocrine/Neuroendocrine Therapeutics
Description

TE-8214 is a long-acting octreotide analog developed using the fatty acid bundle platform for the treatment of acromegaly and neuroendocrine tumors (NETs). It features a water-soluble formulation enabling pain-free subcutaneous injection with thin 30G needles versus 19-20G needles for current LAR formulations. Phase I results showed 83% of high-dose participants achieved >20% IGF-1 reduction with no injection site pain or nodules.

3TE-6168
CategoryCardiovascular/Thrombolytic Therapeutics
Description

TE-6168 is a novel targeted thrombolytic fusion protein for the treatment of ischemic stroke and myocardial infarction. It demonstrated stronger binding activity to human clots than alteplase, reteplase, and tenecteplase (p<0.0001) with milder internal bleeding side effects. TE-6168 has been designated as a CDE Significant Case by Taiwan's Center for Drug Evaluation.

4Multi-arm Linker Technology Platform
CategoryDrug Development Platform Technology
Description

The Multi-arm Linker Technology Platform is a proprietary pharmaceutical design system based on novel multi-arm linkers with a core composed of short peptides of natural amino acids and PEGylated amino acids (2-6 EG units), bearing 2+ linking arms and one coupling arm. Functional groups at ends enable conjugation with targeting or effector elements, forming the basis for licensing and co-development partnerships.

5Fatty Acid Bundle Platform
CategoryDrug Development Platform Technology
Description

The Fatty Acid Bundle Platform uses packed multi-arm linkers carrying 2-3 fatty acid molecules (typically long-chain fatty acids) conjugated at specific amino acid residues (e.g., lysine) or N/C terminals of peptides. This enhances association with serum albumin to prolong circulation half-life, enabling the development of ultra-long-acting drug candidates for endocrine and metabolic diseases.

Scale indicator7 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2025-06-24
Description

T-E Meds and Asymchem signed strategic cooperation agreement for innovative drug development in conjugated therapeutics. Asymchem will leverage T-E Pharma's cytotoxic payload bundle platform to expand ADC capabilities for clients. Scope includes CDMO and clinical CRO services for ADCs and other innovative drug candidates.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2023-09-01
Description

T-E Meds and CHO Pharma provide complementary technologies combining CHO Pharma's glycan modification with T-E Meds' Drug Bundles to form a robust ADC development platform. The 'CHO-TEM' technology enables precise site-specific conjugation through straightforward process, creating homogeneous ADCs with high DAR (8 or 12) and dual-payload capabilities.

3T-E Pharma Holding
Strategic tierCoreTypeOthers
Description

Immunwork is a wholly owned subsidiary of T-E Pharma Holding (Cayman Island company). T-E Pharma serves as capital and strategic integration platform. Parent company also owns T-E Meds Inc. and is targeting TPEx Emerging Stock Board listing in Q4 2026.

immunwork.com
4T-E Meds, Inc.
Strategic tierCoreTypeOthers
Description

T-E Meds is Immunwork's sister company, established in 2022, focusing on ADC and ARC technology platforms and anticancer drug development. While Immunwork develops fatty acid bundle-based drugs, T-E Meds develops antibody-drug conjugates and antibody-radionuclide conjugates using multi-arm linker technologies.

immunwork.com
Recent move9 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

China-based biotech developing biologics including GLP-1 receptor agonists and ADCs. Comparable in clinical-stage pipeline development, multi-modality approach, and Asia-based operations seeking global pharma partnerships.

TypeDirect peer
Description

Clinical-stage biotech developing novel ADCs with proprietary linker platforms (Dolasynthen, Immunosynthen). Comparable as an ADC platform company pursuing differentiated conjugation chemistry and licensing/partnership strategies.

TypeDirect peer
Description

Germany-based biotech developing next-generation ADCs with proprietary linker technologies enabling differentiated payload conjugation. Comparable as a platform-based ADC developer pursuing licensing deals with major pharma.

TypeBroad incumbent
Description

ADC pioneer now part of AbbVie, with multiple approved ADCs (Elahere) and deep pipeline. Comparable as an established ADC platform developer demonstrating scale that newer entrants must compete against.

TypeDirect peer
Description

Clinical-stage biotech developing long-acting somatostatin analogs (paltusotine) for acromegaly and NETs - directly competing with TE-8214. Comparable therapeutic focus on ultra-long-acting endocrine peptides.

TypeEmerging player
Description

China-based clinical-stage biotech developing long-acting GLP-1 receptor agonists for obesity and metabolic disease. Comparable therapeutic focus to TE-8105 with similar half-life extension strategies.

TypeBroad incumbent
Description

Sweden-based specialty pharma with FluidCrystal long-acting depot technology for peptides. Comparable expertise in ultra-long-acting injectable peptide formulations serving similar endocrine/metabolic disease markets.

TypeEmerging player
Description

China/US-based clinical-stage biotech developing ADCs and bispecific antibodies using proprietary antibody engineering platforms. Comparable Asia-based clinical-stage biotech with platform approach to biologic drug development.

TypeEmerging player
Description

China-based biotech with bispecific antibodies and ADCs in clinical development. Comparable Asia-based clinical-stage company developing novel biologics with global pharma licensing strategy.

TypeOthers
Description

China-based global biologics CDMO providing ADC manufacturing and development services. Comparable as an enabler in the ADC ecosystem; Immunwork/T-E Meds partners with CDMOs like Asymchem for similar capabilities.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks6 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

Each record includes

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

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

Feature6 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

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds1 record

Each record includes

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

Investors5 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 →

Immunwork

Biopharmaceuticalsimmunwork.com

Immunwork is a clinical-stage Taiwanese biotech developing ultra-long-acting therapeutics for metabolic, endocrine, and cardiovascular diseases using its proprietary multi-arm linker and fatty acid bundle platforms, operating alongside sister company T-E Meds under T-E Pharma Holding.

What Immunwork does

Immunwork, Inc. (免疫功坊股份有限公司) is a clinical-stage biotechnology company founded in October 2014 in Taipei, Taiwan, operating as a wholly owned subsidiary of Cayman Islands-incorporated T-E Pharma Holding. The company develops ultra-long-acting drug candidates for endocrine, metabolic, and cardiovascular diseases using its proprietary T-E pharmaceutical technology platform, which combines targeting (T) and effector (E) moieties through novel multi-arm linkers. Its lead technology, the Fatty Acid Bundle platform, conjugates 2-3 fatty acid molecules to therapeutic peptides to enhance serum albumin binding and extend circulation half-life, with sister company T-E Meds (established 2022) extending the platform into antibody-drug conjugates (ADCs) and antibody-radionuclide conjugates (ARCs) for oncology applications.

The company's clinical pipeline includes TE-8105, a long-acting GLP-1 receptor agonist for type 2 diabetes and obesity that completed Phase 1/2a trials in Australia in 2025; TE-8214, a long-acting octreotide analog for acromegaly and neuroendocrine tumors that completed Phase I in 2025; TE-6168, a thrombolytic fusion protein for ischemic stroke and myocardial infarction; and TE-1146, an ADC for multiple myeloma licensed to Orient EuroPharma. The company has raised approximately USD 45 million across Immunwork funding rounds (2021 Series A and 2022 A-round) plus USD 26 million for T-E Meds, and collected an USD 8.5 million upfront licensing payment from Orient EuroPharma in January 2025.

Immunwork's revenue model is entirely licensing- and partnership-driven, with no commercialized products. The company generates revenue through upfront licensing fees, development milestones, and royalties upon partner commercialization, supported by a partnership ecosystem that includes Orient EuroPharma (commercial licensee for TE-1146), Asymchem Laboratories (CDMO and CRO services), CHO Pharma (CHO-TEM joint technology), and prospective global pharmaceutical partners accessed via industry conferences including BIO Asia-Taiwan, the J.P. Morgan Healthcare Conference, and World ADC conferences. The parent T-E Pharma Holding is targeting a TPEx Emerging Stock Board listing in Q4 2026 to provide a public capital exit while retaining the holding structure.

Immunwork firmographics

Firmographics
Name
Immunwork
Legal name
免疫功坊股份有限公司 (Immunwork, Inc.)
Website
https://immunwork.com
Company type
Private
Founded year
2014
Operating status
Operating
Headcount range
11–50 employees
Short description
Immunwork is a clinical-stage Taiwanese biotech developing ultra-long-acting therapeutics for metabolic, endocrine, and cardiovascular diseases using its proprietary multi-arm linker and fatty acid bundle platforms, operating alongside sister company T-E Meds under T-E Pharma Holding.
Ownership category
akta.pro rank

Immunwork industry classification

Industry
Product category
Biopharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), Research and Development in Biotechnology (except Nanobiotechnology) (541714), Pharmaceutical Preparation Manufacturing (325412)
SIC
Biological Products, (No Disgnostic Substances) (2836), Pharmaceutical Preparations (2834)
akta.pro primary industry
Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering) (HLAAAIAB)
akta.pro secondary industries
Antibody-Drug Conjugates (ADCs) & Antibody Conjugates (HLAAAAAE), Endocrinology & Reproductive Health Pharmaceuticals (incl. Women’s Health) (HLAIAAAJ)

Keywords

  • Ultra-long-acting peptides
  • Antibody-drug conjugates
  • Fatty acid bundle platform
  • Multi-arm linker technology
  • Clinical-stage biopharmaceuticals

Where Immunwork is headquartered

Location

Headquarters

HQ city
Taipei
HQ country
Taiwan
HQ region
Asia

Offices1 record

Markets served

Immunwork business model

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

Revenue model

  1. Drug Development and Licensing: Pre-revenue clinical-stage biotech company. Revenue expected from out-licensing of drug candidates, milestone payments, and royalties from commercialization. TE-1146 licensing to Orient EuroPharma generated USD 8.5 million upfront.
  2. Strategic Partnerships and Collaborations: Co-development arrangements with pharmaceutical partners for T-E product candidates, potentially generating upfront fees, development milestones, and commercialization revenues.
  3. Platform Technology Licensing: Licensing of multi-arm linker platforms to design new drugs for various disease indications, generating technology access fees and ongoing collaboration payments.

Go-to-market motion3 records

Distribution channels3 records

Marketing channels5 records

Immunwork product offering

Product offering

Core offering

Immunwork is a clinical-stage biotechnology company developing ultra-long-acting drug candidates using its proprietary T-E (targeting and effector) pharmaceutical platform. The company leverages fatty acid bundle technology to create drug candidates with extended half-lives for metabolic diseases (diabetes, obesity), endocrine disorders (acromegaly, neuroendocrine tumors), and cardiovascular conditions (thrombolytic therapy). Its sister company T-E Meds extends the platform to antibody-drug conjugates (ADCs) and antibody-radionuclide conjugates (ARCs) for oncology indications.

Differentiator

Problem solved

Functional benefit

Products and services

  • TE-8105 TE-8105 is a long-acting GLP-1 receptor agonist developed using the fatty acid bundle platform for the treatment of type 2 diabetes, obesity, and non-alcoholic fatty liver disease (NAFLD/NASH). It demonstrated a half-life of 15 hours in mice versus 7.5 hours for semaglutide, enabling potential once-every-two-weeks dosing with superior glucose control and weight loss in preclinical models. Phase 1/2a results showed 5 of 8 participants in B2 cohort achieved >5% body weight reduction.
  • TE-8214 TE-8214 is a long-acting octreotide analog developed using the fatty acid bundle platform for the treatment of acromegaly and neuroendocrine tumors (NETs). It features a water-soluble formulation enabling pain-free subcutaneous injection with thin 30G needles versus 19-20G needles for current LAR formulations. Phase I results showed 83% of high-dose participants achieved >20% IGF-1 reduction with no injection site pain or nodules.
  • TE-6168 TE-6168 is a novel targeted thrombolytic fusion protein for the treatment of ischemic stroke and myocardial infarction. It demonstrated stronger binding activity to human clots than alteplase, reteplase, and tenecteplase (p<0.0001) with milder internal bleeding side effects. TE-6168 has been designated as a CDE Significant Case by Taiwan's Center for Drug Evaluation.
  • Multi-arm Linker Technology Platform The Multi-arm Linker Technology Platform is a proprietary pharmaceutical design system based on novel multi-arm linkers with a core composed of short peptides of natural amino acids and PEGylated amino acids (2-6 EG units), bearing 2+ linking arms and one coupling arm. Functional groups at ends enable conjugation with targeting or effector elements, forming the basis for licensing and co-development partnerships.
  • Fatty Acid Bundle Platform The Fatty Acid Bundle Platform uses packed multi-arm linkers carrying 2-3 fatty acid molecules (typically long-chain fatty acids) conjugated at specific amino acid residues (e.g., lysine) or N/C terminals of peptides. This enhances association with serum albumin to prolong circulation half-life, enabling the development of ultra-long-acting drug candidates for endocrine and metabolic diseases.

Quantifiable outcome

  • TE-8105 demonstrated half-life of 15 hours in mice, approximately 2x that of semaglutide (7.5 hours)
  • +5 more outcomes

Companies that use Immunwork

Customer profile

Named customers1 record

Segments4 records

Ideal customer profiles2 records

Immunwork technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature6 records

Immunwork partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core.

  • Asymchem LaboratoriescoreStrategic or Co-development Partner · 24 June 2025T-E Meds and Asymchem signed strategic cooperation agreement for innovative drug development in conjugated therapeutics. Asymchem will leverage T-E Pharma's cytotoxic payload bundle platform to expand ADC capabilities for clients. Scope includes CDMO and clinical CRO services for ADCs and other innovative drug candidates.
  • CHO PharmacoreStrategic or Co-development Partner · 1 September 2023T-E Meds and CHO Pharma provide complementary technologies combining CHO Pharma's glycan modification with T-E Meds' Drug Bundles to form a robust ADC development platform. The 'CHO-TEM' technology enables precise site-specific conjugation through straightforward process, creating homogeneous ADCs with high DAR (8 or 12) and dual-payload capabilities.
  • T-E Pharma HoldingcoreOthersImmunwork is a wholly owned subsidiary of T-E Pharma Holding (Cayman Island company). T-E Pharma serves as capital and strategic integration platform. Parent company also owns T-E Meds Inc. and is targeting TPEx Emerging Stock Board listing in Q4 2026.
  • T-E Meds, Inc.coreOthersT-E Meds is Immunwork's sister company, established in 2022, focusing on ADC and ARC technology platforms and anticancer drug development. While Immunwork develops fatty acid bundle-based drugs, T-E Meds develops antibody-drug conjugates and antibody-radionuclide conjugates using multi-arm linker technologies.

Scale indicators7 records

Recent moves9 records

Expansion highlights6 records

Immunwork competitors and assessment

Company assessment

Direct peers

  • Innovent Biologics: China-based biotech developing biologics including GLP-1 receptor agonists and ADCs. Comparable in clinical-stage pipeline development, multi-modality approach, and Asia-based operations seeking global pharma partnerships.
  • Mersana Therapeutics: Clinical-stage biotech developing novel ADCs with proprietary linker platforms (Dolasynthen, Immunosynthen). Comparable as an ADC platform company pursuing differentiated conjugation chemistry and licensing/partnership strategies.
  • Tubulis: Germany-based biotech developing next-generation ADCs with proprietary linker technologies enabling differentiated payload conjugation. Comparable as a platform-based ADC developer pursuing licensing deals with major pharma.
  • Crinetics Pharmaceuticals: Clinical-stage biotech developing long-acting somatostatin analogs (paltusotine) for acromegaly and NETs - directly competing with TE-8214. Comparable therapeutic focus on ultra-long-acting endocrine peptides.

Broad incumbents

  • ImmunoGen (AbbVie): ADC pioneer now part of AbbVie, with multiple approved ADCs (Elahere) and deep pipeline. Comparable as an established ADC platform developer demonstrating scale that newer entrants must compete against.
  • Camurus: Sweden-based specialty pharma with FluidCrystal long-acting depot technology for peptides. Comparable expertise in ultra-long-acting injectable peptide formulations serving similar endocrine/metabolic disease markets.

Emerging players

  • Sciwind Biosciences: China-based clinical-stage biotech developing long-acting GLP-1 receptor agonists for obesity and metabolic disease. Comparable therapeutic focus to TE-8105 with similar half-life extension strategies.
  • Adagene: China/US-based clinical-stage biotech developing ADCs and bispecific antibodies using proprietary antibody engineering platforms. Comparable Asia-based clinical-stage biotech with platform approach to biologic drug development.
  • Akeso: China-based biotech with bispecific antibodies and ADCs in clinical development. Comparable Asia-based clinical-stage company developing novel biologics with global pharma licensing strategy.

Others

  • WuXi Biologics: China-based global biologics CDMO providing ADC manufacturing and development services. Comparable as an enabler in the ADC ecosystem; Immunwork/T-E Meds partners with CDMOs like Asymchem for similar capabilities.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks6 records

Key highlights7 records

Customer concentration

Immunwork social profiles

Digital presence

Immunwork financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Immunwork leadership team

Management profile

Number of profiles

Profiles10 records

Immunwork funding detail

Funding detail

Funding overview

Funding rounds1 record

Investors5 records

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

Immunwork 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 Immunwork

What does Immunwork do?

Immunwork is a clinical-stage biotechnology company developing ultra-long-acting drug candidates using its proprietary T-E (targeting and effector) pharmaceutical platform. The company leverages fatty acid bundle technology to create drug candidates with extended half-lives for metabolic diseases (diabetes, obesity), endocrine disorders (acromegaly, neuroendocrine tumors), and cardiovascular conditions (thrombolytic therapy). Its sister company T-E Meds extends the platform to antibody-drug conjugates (ADCs) and antibody-radionuclide conjugates (ARCs) for oncology indications.

Is Immunwork a public or private company?

Immunwork is a private company. It is classified as corporate owned and is currently operating.

When was Immunwork founded?

Immunwork was founded in 2014. It employs 11 to 50 people.

Where is Immunwork based?

Immunwork is headquartered in Taipei, Taiwan, in the Asia region.

How does Immunwork make money?

Three revenue lines are on record. Drug Development and Licensing is the primary driver. The others are strategic Partnerships and Collaborations and platform Technology Licensing.

Who are Immunwork's main competitors?

Direct peers on record are Innovent Biologics, Mersana Therapeutics, Tubulis and Crinetics Pharmaceuticals. Broad incumbents are ImmunoGen (AbbVie) and Camurus. Emerging players are Sciwind Biosciences, Adagene and Akeso. WuXi Biologics is listed as an others.

Does Immunwork have an API?

No public API is recorded for Immunwork.

What industry is Immunwork in?

Immunwork's product category is Biopharmaceuticals. Its primary akta.pro industry code is HLAAAIAB, Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering), 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
Tech TimesBiweekly GLP-1 Drug Clears First Human Test via Dual Fatty Acid EngineeringTaiwanese biotech Immunwork published first-in-human Phase 1/2a data for TE-8105, a GLP-1 drug utilizing dual fatty acid engineering to achieve a 120-hour plasma half-life suitable for biweekly dosing. The trial confirmed the drug's safety and tolerability while demonstrating metabolic benefits, positioning it alongside Pfizer's berobenatide as an alternative approach to less frequent injection regimens in the competitive obesity treatment market.GbimonthlyThe Father of Antibodies, Zhang Ziwen, has raised 670 million yuan in Round A funding to seize licensing opportunities - Global Biotechnology Monthly.ImmunoWorks, founded by antibody expert Zhang Ziwen, completed a Series A funding round of 24 million USD in March to advance its T-E™ platform. The company has derived six new drug product lines, with two expected to enter clinical trials next year. This development highlights ongoing efforts in Taiwan's biotech sector despite reported insufficiencies in local support.ImmunworkImmunoWorks completes round A fundraising of 670 million! Six new drug products have achieved efficacy verification!ImmunoWorks completed a Series A fundraising round of 670 million and announced that six new drug products have achieved efficacy verification. The company utilizes its patented T-E Technology Platform, which employs multi-arm linkers and drug bundles to combine targets and efficacy components into single molecules.