Cho Pharma
CHO PHARMA INC. (Taiwan, TWSE: 6586) is a clinical-stage biotechnology company developing glycoengineered biobetter antibodies, glycosite-specific ADCs, and carbohydrate-conjugate vaccines using its proprietary one-pot enzymatic CHOptimax™ platform, licensing the technology and co-developing products with pharmaceutical partners.
- Company typePublic
- Founded2013
- HeadquartersTaipei, Taiwan
- Headcount1–10
- GTM typeB2B
- OfferingServices
What Cho Pharma does
CHO PHARMA INC. (醣基) is a Taiwan-based biotechnology company founded in 2013 and listed on the Taiwan Stock Exchange (TWSE: 6586). It is built around a proprietary enzymatic glycoengineering platform called CHOptimax™, which uses a one-pot reaction with a single enzyme and a single substrate to convert off-the-shelf antibodies into either glycoengineered biobetters or glycosite-specific antibody-drug conjugates (ADCs). The company is led by Chairman Dr. Chao-Long Chen and President & CEO Dr. Chung-Yi Wu, with scientific origins in Academia Sinica's glycoscience research community, including lineage to Prof. Chi-Huey Wong. Its IP portfolio comprises 60+ granted patents and 20+ pending applications covering the platform, proprietary enzymes, and product compositions.
The company's product portfolio spans glycoengineered biobetter antibodies (CHO-H01 targeting CD20 in refractory non-Hodgkin lymphoma, in Phase I/IIa; CHO-H02 targeting HER2; CHO-H03 for autoimmune indications), a humanized monoclonal antibody targeting SSEA-4 on cancer stem cells (CHO-A04, Phase I/IIa in advanced solid tumors), and a bivalent carbohydrate-conjugate vaccine against Klebsiella pneumoniae serotypes K1 and K2 (CHO-V08, Phase 1). CHO-H01 is described as the world's first glycoengineered biobetter, with preclinical data showing a 30–50 fold increase in ADCC activity versus non-glycoengineered rituximab. The company also offers contract manufacturing services to produce glycoengineered antibodies and glycosite-specific ADCs for research and pre-clinical use by external partners.
CHO PHARMA is pre-commercial. Its revenue model rests on three pillars: (1) licensing of the CHOptimax™ platform technology to pharmaceutical partners, (2) co-development of biobetters and ADCs with strategic partners for downstream commercialization economics, and (3) contract research and manufacturing services for glycoengineered antibodies and ADCs. Operating revenue to date has been episodic and modest, in the low single-digit US$ million range on an annualized basis, with reported EBITDA and operating income deeply negative across 2021–2025 reflecting continued heavy R&D investment. The principal customers in its current model are pharmaceutical partners seeking to license the platform or co-develop products, with end-patient populations (oncology, autoimmune, infectious disease) being downstream beneficiaries rather than direct customers. Capital is being raised in part through a private placement of up to 30,000,000 new shares, with major institutional shareholders including Fubon Financial, Fubon Life, and Nestor Capital.
Cho Pharma firmographics
Firmographics- Name
- Cho Pharma
- Legal name
- CHO PHARMA INC. 醣基
- Website
- https://chopharma.com
- Company type
- Public
- Founded year
- 2013
- Operating status
- Operating
- Headcount range
- 1–10 employees
- Short description
- CHO PHARMA INC. (Taiwan, TWSE: 6586) is a clinical-stage biotechnology company developing glycoengineered biobetter antibodies, glycosite-specific ADCs, and carbohydrate-conjugate vaccines using its proprietary one-pot enzymatic CHOptimax™ platform, licensing the technology and co-developing products with pharmaceutical partners.
- Ownership category
- akta.pro rank
Cho Pharma industry classification
Industry- Product category
- Biopharmaceuticals (Glycoengineered Antibody Drugs)
- NAICS
- Biological Product (except Diagnostic) Manufacturing (325414), Pharmaceutical and Medicine Manufacturing (3254)
- 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), Monoclonal Antibody Therapeutics (mAbs) (HLAAAAAA), Immunology & Inflammation Pharmaceuticals (HLAIAAAD), Clinical Development & Regulatory for Vaccines (trials, pharmacovigilance, lot release) (HLAAAEAK)
Keywords
Where Cho Pharma is headquartered
LocationHeadquarters
- HQ city
- Taipei
- HQ country
- Taiwan
- HQ region
- Asia
Offices1 record
Markets served
Cho Pharma business model
Business model- GTM type
- B2B
- Offering type
- Services
- Cost components
- Technology or R&D, Personnel, Operations, Marketing or Sales
Revenue model
- Technology Licensing: CHOptimax™ platform technology licensing to pharmaceutical partners for drug development.
- Product Co-development: Co-development of glycoengineered biobetters and ADCs with strategic partners, potentially leading to product commercialization revenue.
- Contract Research Services: Providing services to produce glycoengineered antibodies and glycosite-specific ADCs for research and pre-clinical evaluation.
Go-to-market motion1 record
Distribution channels1 record
Marketing channels3 records
Cho Pharma product offering
Product offeringCore offering
CHO Pharma develops the proprietary CHOptimax™ one-pot enzymatic glycoengineering platform to convert naked antibodies into glycoengineered biobetters or glycosite-specific antibody-drug conjugates (ADCs) in a single step. The company operates a clinical-stage pipeline of glycoengineered antibody drug candidates (CHO-H01, CHO-H02, CHO-H03, CHO-A04) and a carbohydrate-based bivalent vaccine (CHO-V08) targeting B-cell malignancies, solid tumors, autoimmune diseases, and Klebsiella pneumoniae infections. It also licenses its platform technology, co-develops products with partners, and offers contract research services to produce glycoengineered antibodies and ADCs for pre-clinical evaluation.
Product overview
Cho Pharma is a Taiwan-based biotechnology company founded in 2013, traded on TWSE (6586), specializing in glycoengineering platform technologies for drug development. The core technology is CHOptimax™, a proprietary one-pot enzymatic platform that enables precise glycosylation control of antibodies. The product portfolio includes glycoengineered biobetter antibodies (CHO-H01, CHO-H02, CHO-H03, CHO-A04) targeting CD20, HER2, undisclosed, and SSEA-4 respectively, a bivalent vaccine (CHO-V08) against Klebsiella pneumonia, and glycosite-specific ADC candidates. CHO-H01 is the world's first glycoengineered biobetter. The company also offers contract manufacturing services for glycoengineered antibodies and ADCs for research and preclinical evaluation.
Differentiator
Problem solved
Functional benefit
Brands
- CHOptimax™: Proprietary glycoengineering platform technology that enables one-step enzymatic conversion of antibodies into glycoengineered biobetters or glycosite-specific ADCs.
Products and services
- CHOptimax™ Glycoengineering Platform Proprietary one-pot enzymatic platform technology that uses one enzyme and one substrate to convert antibodies into glycoengineered biobetters or glycosite-specific ADCs in a single step, with GMP process completion within 24 hours and scalable homogeneous production. Available for technology licensing, co-development, and contract research services for pharmaceutical partners.
- CHO-H01 (Glycoengineered Anti-CD20 Biobetter) Anti-CD20 glycoengineered biobetter antibody drug candidate that delivers a 30-50 fold increase in ADCC activity versus non-glycoengineered Rituximab and shows potent activity against Rituximab-resistant B lymphoma cells. Indicated for B-cell malignancies including refractory non-Hodgkin lymphoma.
- CHO-H02 (HER2-Targeted Glycoengineered Antibody/ADC) Next-generation HER2-targeted antibody drug candidate comprising glycoengineered biobetter and glycosite-specific ADC variants using CHOptimax™ technology. Preclinical development for breast, bladder, pancreatic, ovarian, and gastric cancers.
- CHO-H03 (Anti-Autoimmune Antibody) Antibody drug candidate engineered via CHOptimax™ to increase FcγR binding and induce regulatory macrophages for treatment of autoimmune diseases including rheumatoid arthritis, ulcerative colitis, and Crohn's disease.
- CHO-A04 (Anti-SSEA-4 Antibody) Humanized monoclonal antibody targeting SSEA-4, a glycosphingolipid highly expressed on tumor cells and cancer stem cells. Currently in Phase I/IIa clinical trial for advanced solid tumors.
- CHO-V08 (Klebsiella pneumoniae Bivalent Vaccine) Bivalent carbohydrate-based conjugate vaccine targeting Klebsiella pneumoniae serotypes K1 and K2 to prevent nosocomial infections. Currently in Phase 1 clinical trial.
- Glycoengineered Antibody Manufacturing Service Contract manufacturing services using the CHOptimax™ platform to produce glycoengineered antibodies and glycosite-specific ADCs for research and pre-clinical evaluation by pharmaceutical partners.
Quantifiable outcome
- 30-50 fold increase in ADCC activity compared to non-glycoengineered Rituximab in preclinical studies
- +5 more outcomes
Companies that use Cho Pharma
Customer profileSegments2 records
Ideal customer profiles1 record
Cho Pharma technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature4 records
Cho Pharma partnerships and signals
Strategic signalPartnerships
One partnership is on record.
- Strategic Partners (Seeking)coreCHO Pharma is actively seeking strategic partners with complementary technologies and services to achieve mutual benefits. The company offers CHOptimax™ licensing, product co-development opportunities, and strategic alliance partnerships to bring life-changing medicines for patients with limited or inadequate treatment options.
Scale indicators4 records
Recent moves6 records
Expansion highlights5 records
Cho Pharma competitors and assessment
Company assessmentDirect peers
- OBI Pharma: Taiwan-based, TWSE-listed clinical-stage biotechnology company developing antibody-drug conjugates and glycan-targeted oncology therapeutics. Operates in the same Taiwan oncology biologics ecosystem with a comparable pre-commercial profile and product-platform hybrid structure.
- LegoChem Biosciences: Korean clinical-stage biotech operating a proprietary ADC platform technology (ConjuAll) with site-specific conjugation chemistry and licensing-based monetization. Highly comparable to CHOptimax™ as both are ADC platform plays monetized via partnerships and licensing deals.
- Sutro Biopharma: US-based clinical-stage biotech with cell-free protein synthesis platform for site-specific antibody and ADC development. Operates a hybrid model of internal pipeline plus partner-funded programs, closely mirroring CHO Pharma's technology licensing and co-development strategy.
- AbCellera Biologics: Canadian antibody discovery and engineering platform that partners with biopharma to develop therapeutic antibodies using its proprietary screening technology. Comparable as a platform-revenue model biotech with similar technology-licensing, co-development, and partnership-driven revenue streams.
- Innate Pharma: French clinical-stage immuno-oncology company leveraging antibody platform technologies (NK-cell engagers, ADC payloads) with both internal pipeline and pharma partnerships. Comparable as a non-revenue antibody platform biotech pursuing oncology indications.
Broad incumbents
- Genmab: Danish commercial-stage antibody therapeutics company with proprietary DuoBody (bispecific) and HexaBody platforms that license to major pharma partners. A mature incumbent demonstrating the platform-licensing business model at scale, with multiple validating partnerships.
- ImmunoGen: US-based pioneer in ADC development with proprietary linker-payload technology and multiple approved/partnered ADC assets, now part of AbbVie. Represents the validation endpoint and ultimate exit model for ADC platform companies.
Regional players
- Acepodia: Taiwan-based clinical-stage biotech with antibody-drug conjugate (ACC) and antibody-cell effector (ACE) platform technologies targeting oncology. Regional direct peer operating in the same Taiwan biotech ecosystem with adjacent antibody platform technology.
- PharmaEssentia: Taiwan-based, TWSE-listed specialty biotech (mkt-listed) with a commercially launched biologic (Besremi) and ongoing pipeline. Comparable as a Taiwan-headquartered, exchange-listed biotech investor benchmark, though at a more advanced commercial stage.
Others
- WuXi Biologics: China-headquartered global biologics CDMO operating large-scale antibody manufacturing services for pharma partners. Relevant as an enabling service provider/ecosystem participant that CHO Pharma's contract research offering competes against or partners with.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks6 records
Key highlights7 records
Customer concentration
Cho Pharma social profiles
Digital presenceCho Pharma financial estimates
Financial estimateRevenue estimate
Valuation estimate
Cho Pharma leadership team
Management profileNumber of profiles
Profiles4 records
Cho Pharma funding detail
Funding detailFunding overview
Funding rounds
Investors
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Cho Pharma M&A and investment
M&A and investmentM&A
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Cho Pharma
What does Cho Pharma do?
CHO Pharma develops the proprietary CHOptimax™ one-pot enzymatic glycoengineering platform to convert naked antibodies into glycoengineered biobetters or glycosite-specific antibody-drug conjugates (ADCs) in a single step. The company operates a clinical-stage pipeline of glycoengineered antibody drug candidates (CHO-H01, CHO-H02, CHO-H03, CHO-A04) and a carbohydrate-based bivalent vaccine (CHO-V08) targeting B-cell malignancies, solid tumors, autoimmune diseases, and Klebsiella pneumoniae infections. It also licenses its platform technology, co-develops products with partners, and offers contract research services to produce glycoengineered antibodies and ADCs for pre-clinical evaluation.
Is Cho Pharma a public or private company?
Cho Pharma is a public company. It is classified as public and is currently operating.
When was Cho Pharma founded?
Cho Pharma was founded in 2013. It employs 1 to 10 people.
Where is Cho Pharma based?
Cho Pharma is headquartered in Taipei, Taiwan, in the Asia region.
How does Cho Pharma make money?
Three revenue lines are on record. Technology Licensing is the primary driver. The others are product Co-development and contract Research Services.
Who are Cho Pharma's main competitors?
Direct peers on record are OBI Pharma, LegoChem Biosciences, Sutro Biopharma, AbCellera Biologics and Innate Pharma. Broad incumbents are Genmab and ImmunoGen. Regional players are Acepodia and PharmaEssentia. WuXi Biologics is listed as an others.
Does Cho Pharma have an API?
No public API is recorded for Cho Pharma.
What industry is Cho Pharma in?
Cho Pharma's product category is Biopharmaceuticals (Glycoengineered Antibody Drugs). 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.