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RemeGen荣昌生物

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uuid00vikxf

Namestring
RemeGen荣昌生物
Legal namestring
荣昌生物制药(烟台)股份有限公司
Websiteurl
remegen.cn
Company typeenum
Public
Founded yearint
2008
Descriptiontext

RemeGen Co., Ltd. (荣昌生物制药(烟台)股份有限公司, 688331.SH / 09995.HK) is a China-headquartered biopharmaceutical company founded in 2008 by Wang Weidong and Dr. Fang Jianmin, developing, manufacturing, and commercializing innovative biologic drugs for autoimmune diseases, oncology, and ophthalmology. Its commercial portfolio comprises two core products: Telitacicept (RC18, brand 泰爱®), the world's first BLyS/APRIL dual-target fusion protein biologic with five NMPA-approved indications (SLE, RA, gMG, Sjogren's syndrome, and IgA nephropathy), and Disitamab Vedotin (RC48, brand 爱地希®), China's first domestically developed HER2-targeting antibody-drug conjugate (ADC) approved for gastric cancer, urothelial carcinoma, and HER2-expressing breast cancer. The underlying platform technology spans proprietary antibody fusion protein engineering, ADC technology with novel toxins and linkers, bispecific antibodies (including PD-1/VEGF), and a next-generation Payload Recovery ADC (PR-ADC) platform — backed by 600+ patent applications and 40+ active clinical trials across eight clinical-stage pipeline programs.

Short descriptiontext

RemeGen (荣昌生物) is a China-based A+H-listed biopharmaceutical company that develops, manufactures, and commercializes first-in-class biologics including Telitacicept (BLyS/APRIL dual-target fusion protein for autoimmune diseases) and Disitamab Vedotin (HER2 ADC for oncology), serving Chinese hospitals across autoimmune, oncology, and ophthalmology therapeutic areas.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersYantai, China
HQ citystring
Yantai
HQ countrystring
China
HQ regionstring
Asia
Markets served

Serves global market

Offices4 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
biologic drug development, antibody drug conjugates, autoimmune disease therapeutics, oncology biologics, fusion protein drugs
Industry4 codes
1Antibody Discovery & Engineering Platforms (display tech, bispecifics, Fc engineering)
CodeHLAAAIABPrimaryYes
2Recombinant Protein Therapeutics (enzymes, hormones, growth factors)
CodeHLAAAAABPrimaryNo
3Antibody-Drug Conjugates (ADCs) & Antibody Conjugates
CodeHLAAAAAEPrimaryNo
4Immunology & Autoimmune Specialty Pharmaceuticals
CodeHLAIACABPrimaryNo
NAICS code2 codes
  • Biological Product (except Diagnostic) Manufacturing325414
  • Pharmaceutical Preparation Manufacturing325412
SIC code2 codes
  • Biological Products, (No Disgnostic Substances)2836
  • Pharmaceutical Preparations2834
Product category
Biopharmaceuticals
No data
GTM motion2 records

Each record includes

Type, Description, Source

Revenue model3 records
1Domestic Product Sales
TypeSubscription Recurring
Description

Domestic commercial sales of approved products including Telitacicept (RC18) and Disitamab Vedotin (RC48). 2025 domestic sales reached 22.71 billion RMB, growing 34% YoY. Continuous growth driven by hospital access expansion and new indication approvals.

remegen.cn
2BD Licensing/Out-licensing
TypeLicensing Royalties
Description

Upfront payments, milestone payments, and royalties from out-licensing agreements with global pharmaceutical partners. RC48 licensed to Seagen (2021) for $2.6B; RC18 licensed to Vor Bio for $4.23B; RC28 licensed to Santen for ~RMB 1.275B; RC148 licensed to AbbVie for $5.6B including $650M upfront.

remegen.cn
3Milestone Payments
TypeLicensing Royalties
Description

Development, regulatory, and commercial milestone payments from partnership agreements, contributing significant non-recurring revenue.

remegen.cn
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels2 records

Each record includes

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

Cost components5 values
Personnel, Technology or R&D, Marketing or Sales, Supply Chain, Operations
Pricing details1 tier
1Hospital tender-based pricing with NRDL reimbursement
ModelSubscriptionBilling cadenceAnnual
Notes

Products sold through hospital tender process and reimbursed through National Medical Insurance. Price varies by province and hospital. 2025 drug price negotiation resulted in approximately 10% price reduction for core products.

remegen.cn
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 2 records shown
1泰爱®
Description

泰它西普(RC18)的商品名,BLyS/APRIL双靶点融合蛋白创新药,用于治疗系统性红斑狼疮、类风湿关节炎、全身型重症肌无力、干燥综合征、IgA肾病等自身免疫疾病。

remegen.cn
+1 more record
Core offering1 text field

RemeGen discovers, develops, manufactures, and commercializes innovative biologic drugs targeting autoimmune diseases, oncology, and ophthalmology. Its commercial portfolio includes Telitacicept (RC18), the world's first BLyS/APRIL dual-target fusion protein biologic, and Disitamab Vedotin (RC48), China's first domestically developed HER2-targeting antibody-drug conjugate (ADC). The company also licenses its pipeline assets to global pharmaceutical partners for international markets.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 5 values shown
  • Telitacicept achieved 55% UPCR reduction vs placebo (p<0.0001) in IgA nephropathy Phase III
+4 more records
Product overview1 text field

RemeGen荣昌生物 is a biopharmaceutical company that discovers, develops, manufactures, and commercializes innovative biologic drugs. The company's portfolio includes two marketed products: 泰它西普 (Telitacicept/RC18), a BLyS/APRIL dual-target fusion protein for autoimmune diseases, and 维迪西妥单抗 (Disitamab vedotin/RC48), China's first self-developed HER2-targeting ADC for oncology. The pipeline includes multiple bispecific antibodies and ADCs such as RC148 (PD-1/VEGF bispecific), RC28 (ophthalmology), RC88, RC278, and RC288 (PSMA/B7H3 bispecific ADC), covering autoimmune diseases, oncology, and ophthalmology therapeutic areas.

Product and service2 records
1Telitacicept (RC18) / 泰它西普 (Brand: 泰爱®)
CategoryBiologic drug (fusion protein)
Description

World's first BLyS/APRIL dual-target fusion protein innovative biologic drug for autoimmune diseases. Indicated for SLE, RA, gMG, Sjogren's syndrome, and IgA nephropathy. Targets B-cell activating factor and a proliferation-inducing ligand pathways.

2Disitamab Vedotin (RC48) / 维迪西妥单抗 (Brand: 爱地希®)
Scale indicator13 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2026-01-01
Description

Licensing agreement for RC148 (PD-1/VEGF bispecific antibody). AbbVie获得RC148在大中华区以外地区的独家开发、生产和商业化权利。荣昌生物获得6.5亿美元首付款,并有资格获得最高达49.5亿美元的开发、监管和商业化里程碑付款,以及两位数分级特许权使用费。总交易额56亿美元。

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2025-06-01
Description

Licensing agreement for RC18 (Telitacicept) covering global markets outside Greater China. Vor Bio received rights for global development of autoimmune indications including myasthenia gravis and Sjogren's syndrome. Deal includes $45M upfront, $80M warrant, up to $4.105B milestones, and high single-digit to double-digit royalties. Total deal value $4.23B.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2025-01-01
Description

Licensing agreement for RC28 (VEGF/FGF dual-target fusion protein) for ophthalmology. Covers Greater China and multiple Asian markets. Deal includes 250M RMB upfront, up to 520M RMB development milestones, up to 525M RMB sales milestones, and tiered royalties.

Strategic tierCoreTypeOEM/ Whitelabel/ Licensing PartnerAnnounced on2021-08-01
Description

Licensing agreement for RC48 (Disitamab Vedotin). Original deal valued at $2.6 billion. Seagen获得RC48在大中华区以外的全球独家开发、生产和商业化权利。

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight5 records

Each record includes

Type, Description

Peers10 records
TypeBroad incumbent
Description

Daiichi Sankyo is the global ADC platform leader (Enhertu/Datroway) with HER2 and Trop-2 franchises that directly compete with RemeGen's Disitamab Vedotin. As a larger established Japanese pharma with deep ADC technology, it represents the dominant incumbent whose commercial success benchmarks the upside ceiling for HER2 ADC class.

TypeBroad incumbent
Description

Pfizer acquired Seagen in 2023 and thereby inherited the global development and commercialization rights to RC48 (Disitamab Vedotin) under the original 2021 USD 2.6B licensing deal. Pfizer's strategic priorities for the Seagen ADC pipeline directly shape the international commercialization trajectory of RemeGen's flagship oncology asset.

TypeDirect peer
Description

BeiGene is a globally commercialized Chinese biotech with BRUKINSA (zanubrutinib) as a flagship hematology asset. It offers a comparable profile of China-origin biologics, A+H/US listings, deep commercial infrastructure in China, and global out-licensing/partnership strategy similar to RemeGen's AbbVie and Vor Bio deals.

TypeDirect peer
Description

Akeso is a Chinese biotech with the PD-1/VEGF bispecific ivonescimab that directly competes with RemeGen's RC148 in non-small cell lung cancer and other oncology indications. Both companies are China-based, platform-driven biologic innovators pursuing global out-licensing deals with similar therapeutic focus areas (oncology/immunology).

TypeEmerging player
Description

Cstone is a smaller Chinese biotech with biologic and bispecific antibody assets pursuing similar out-licensing and indication-expansion strategies. While smaller in scale, it represents a comparable emerging Chinese biologic innovator that competes for global partner interest and KOL mindshare in similar indications.

TypeDirect peer
Description

Innovent is a leading Chinese biologics innovator with multiple approved products and PD-1 leadership (sintilimab), pursuing both domestic commercial sales and global BD partnerships. Comparable to RemeGen in therapeutic focus (oncology, autoimmune), biologics platform depth, and commercial model (NRDL-driven hospital sales).

TypeBroad incumbent
Description

AstraZeneca is a global oncology and immunology leader with HER2 ADC (in collaboration with Daiichi Sankyo) and autoimmune biologics (Saphnelo for SLE) that compete with RemeGen's portfolio in both therapeutic areas. Its breadth of operations and global commercial reach establish the scale benchmark for out-licensed RemeGen assets.

TypeBroad incumbent
Description

Hansoh is one of China's leading innovative pharma companies with a deep oncology pipeline and biologic assets competing in similar indications to RemeGen. Comparable as a domestically focused, NRDL-driven commercial player with growing biologic portfolio exposure.

TypeBroad incumbent
Description

Hengrui is China's largest domestic pharmaceutical company with a broad oncology, autoimmune, and biologic pipeline competing directly with RemeGen in Chinese hospital channels. As the largest incumbent, it anchors the competitive dynamics of NRDL negotiations and hospital tender processes that govern RemeGen's domestic commercial trajectory.

TypeDirect peer
Description

Junshi is a Chinese biotech that pioneered PD-1 (toripalimab) and has pursued combination therapies with partners including Coherus. RemeGen's RC48 + toripalimab combination in urothelial carcinoma creates direct clinical collaboration overlap, and Junshi shares RemeGen's A+H dual-listing, biologics platform, and indication-expansion strategy.

Market position
Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 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

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

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles13 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 rounds

Each record includes

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

Investors

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 →

RemeGen荣昌生物

Biopharmaceuticalsremegen.cn

RemeGen (荣昌生物) is a China-based A+H-listed biopharmaceutical company that develops, manufactures, and commercializes first-in-class biologics including Telitacicept (BLyS/APRIL dual-target fusion protein for autoimmune diseases) and Disitamab Vedotin (HER2 ADC for oncology), serving Chinese hospitals across autoimmune, oncology, and ophthalmology therapeutic areas.

What RemeGen荣昌生物 does

RemeGen Co., Ltd. (荣昌生物制药(烟台)股份有限公司, 688331.SH / 09995.HK) is a China-headquartered biopharmaceutical company founded in 2008 by Wang Weidong and Dr. Fang Jianmin, developing, manufacturing, and commercializing innovative biologic drugs for autoimmune diseases, oncology, and ophthalmology. Its commercial portfolio comprises two core products: Telitacicept (RC18, brand 泰爱®), the world's first BLyS/APRIL dual-target fusion protein biologic with five NMPA-approved indications (SLE, RA, gMG, Sjogren's syndrome, and IgA nephropathy), and Disitamab Vedotin (RC48, brand 爱地希®), China's first domestically developed HER2-targeting antibody-drug conjugate (ADC) approved for gastric cancer, urothelial carcinoma, and HER2-expressing breast cancer. The underlying platform technology spans proprietary antibody fusion protein engineering, ADC technology with novel toxins and linkers, bispecific antibodies (including PD-1/VEGF), and a next-generation Payload Recovery ADC (PR-ADC) platform — backed by 600+ patent applications and 40+ active clinical trials across eight clinical-stage pipeline programs.

RemeGen荣昌生物 firmographics

Firmographics
Name
RemeGen荣昌生物
Legal name
荣昌生物制药(烟台)股份有限公司
Website
https://remegen.cn
Company type
Public
Founded year
2008
Operating status
Operating
Headcount range
1–10 employees
Short description
RemeGen (荣昌生物) is a China-based A+H-listed biopharmaceutical company that develops, manufactures, and commercializes first-in-class biologics including Telitacicept (BLyS/APRIL dual-target fusion protein for autoimmune diseases) and Disitamab Vedotin (HER2 ADC for oncology), serving Chinese hospitals across autoimmune, oncology, and ophthalmology therapeutic areas.
Ownership category
akta.pro rank

RemeGen荣昌生物 industry classification

Industry
Product category
Biopharmaceuticals
NAICS
Biological Product (except Diagnostic) Manufacturing (325414), 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
Recombinant Protein Therapeutics (enzymes, hormones, growth factors) (HLAAAAAB), Antibody-Drug Conjugates (ADCs) & Antibody Conjugates (HLAAAAAE), Immunology & Autoimmune Specialty Pharmaceuticals (HLAIACAB)

Keywords

  • Biologic drug development
  • Antibody drug conjugates
  • Autoimmune disease therapeutics
  • Oncology biologics
  • Fusion protein drugs

Where RemeGen荣昌生物 is headquartered

Location

Headquarters

HQ city
Yantai
HQ country
China
HQ region
Asia

Offices4 records

Markets served

RemeGen荣昌生物 business model

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

Revenue model

  1. Domestic Product Sales: Domestic commercial sales of approved products including Telitacicept (RC18) and Disitamab Vedotin (RC48). 2025 domestic sales reached 22.71 billion RMB, growing 34% YoY. Continuous growth driven by hospital access expansion and new indication approvals.
  2. BD Licensing/Out-licensing: Upfront payments, milestone payments, and royalties from out-licensing agreements with global pharmaceutical partners. RC48 licensed to Seagen (2021) for $2.6B; RC18 licensed to Vor Bio for $4.23B; RC28 licensed to Santen for ~RMB 1.275B; RC148 licensed to AbbVie for $5.6B including $650M upfront.
  3. Milestone Payments: Development, regulatory, and commercial milestone payments from partnership agreements, contributing significant non-recurring revenue.

Pricing tiers

ModelBillingPrice
SubscriptionAnnualHospital tender-based pricing with NRDL reimbursement

Go-to-market motion2 records

Distribution channels2 records

Marketing channels4 records

RemeGen荣昌生物 product offering

Product offering

Core offering

RemeGen discovers, develops, manufactures, and commercializes innovative biologic drugs targeting autoimmune diseases, oncology, and ophthalmology. Its commercial portfolio includes Telitacicept (RC18), the world's first BLyS/APRIL dual-target fusion protein biologic, and Disitamab Vedotin (RC48), China's first domestically developed HER2-targeting antibody-drug conjugate (ADC). The company also licenses its pipeline assets to global pharmaceutical partners for international markets.

Product overview

RemeGen荣昌生物 is a biopharmaceutical company that discovers, develops, manufactures, and commercializes innovative biologic drugs. The company's portfolio includes two marketed products: 泰它西普 (Telitacicept/RC18), a BLyS/APRIL dual-target fusion protein for autoimmune diseases, and 维迪西妥单抗 (Disitamab vedotin/RC48), China's first self-developed HER2-targeting ADC for oncology. The pipeline includes multiple bispecific antibodies and ADCs such as RC148 (PD-1/VEGF bispecific), RC28 (ophthalmology), RC88, RC278, and RC288 (PSMA/B7H3 bispecific ADC), covering autoimmune diseases, oncology, and ophthalmology therapeutic areas.

Differentiator

Problem solved

Functional benefit

Brands

  • 泰爱®: 泰它西普(RC18)的商品名,BLyS/APRIL双靶点融合蛋白创新药,用于治疗系统性红斑狼疮、类风湿关节炎、全身型重症肌无力、干燥综合征、IgA肾病等自身免疫疾病。
  • 爱地希®

Products and services

  • Telitacicept (RC18) / 泰它西普 (Brand: 泰爱®) World's first BLyS/APRIL dual-target fusion protein innovative biologic drug for autoimmune diseases. Indicated for SLE, RA, gMG, Sjogren's syndrome, and IgA nephropathy. Targets B-cell activating factor and a proliferation-inducing ligand pathways.
  • Disitamab Vedotin (RC48) / 维迪西妥单抗 (Brand: 爱地希®)

Quantifiable outcome

  • Telitacicept achieved 55% UPCR reduction vs placebo (p<0.0001) in IgA nephropathy Phase III
  • +4 more outcomes

Companies that use RemeGen荣昌生物

Customer profile

Named customers1 record

Segments3 records

Ideal customer profiles2 records

RemeGen荣昌生物 technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

RemeGen荣昌生物 partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core.

  • AbbVie (艾伯维)coreOEM/ Whitelabel/ Licensing Partner · 1 January 2026Licensing agreement for RC148 (PD-1/VEGF bispecific antibody). AbbVie获得RC148在大中华区以外地区的独家开发、生产和商业化权利。荣昌生物获得6.5亿美元首付款,并有资格获得最高达49.5亿美元的开发、监管和商业化里程碑付款,以及两位数分级特许权使用费。总交易额56亿美元。
  • Vor BiocoreOEM/ Whitelabel/ Licensing Partner · 1 June 2025Licensing agreement for RC18 (Telitacicept) covering global markets outside Greater China. Vor Bio received rights for global development of autoimmune indications including myasthenia gravis and Sjogren's syndrome. Deal includes $45M upfront, $80M warrant, up to $4.105B milestones, and high single-digit to double-digit royalties. Total deal value $4.23B.
  • Santen China (参天中国)coreOEM/ Whitelabel/ Licensing Partner · 1 January 2025Licensing agreement for RC28 (VEGF/FGF dual-target fusion protein) for ophthalmology. Covers Greater China and multiple Asian markets. Deal includes 250M RMB upfront, up to 520M RMB development milestones, up to 525M RMB sales milestones, and tiered royalties.
  • SeagencoreOEM/ Whitelabel/ Licensing Partner · 1 August 2021Licensing agreement for RC48 (Disitamab Vedotin). Original deal valued at $2.6 billion. Seagen获得RC48在大中华区以外的全球独家开发、生产和商业化权利。

Scale indicators13 records

Recent moves8 records

Expansion highlights5 records

RemeGen荣昌生物 competitors and assessment

Company assessment

Broad incumbents

  • Daiichi Sankyo: Daiichi Sankyo is the global ADC platform leader (Enhertu/Datroway) with HER2 and Trop-2 franchises that directly compete with RemeGen's Disitamab Vedotin. As a larger established Japanese pharma with deep ADC technology, it represents the dominant incumbent whose commercial success benchmarks the upside ceiling for HER2 ADC class.
  • Pfizer: Pfizer acquired Seagen in 2023 and thereby inherited the global development and commercialization rights to RC48 (Disitamab Vedotin) under the original 2021 USD 2.6B licensing deal. Pfizer's strategic priorities for the Seagen ADC pipeline directly shape the international commercialization trajectory of RemeGen's flagship oncology asset.
  • AstraZeneca: AstraZeneca is a global oncology and immunology leader with HER2 ADC (in collaboration with Daiichi Sankyo) and autoimmune biologics (Saphnelo for SLE) that compete with RemeGen's portfolio in both therapeutic areas. Its breadth of operations and global commercial reach establish the scale benchmark for out-licensed RemeGen assets.
  • Hansoh Pharmaceutical (翰森制药): Hansoh is one of China's leading innovative pharma companies with a deep oncology pipeline and biologic assets competing in similar indications to RemeGen. Comparable as a domestically focused, NRDL-driven commercial player with growing biologic portfolio exposure.
  • Hengrui Pharma (恒瑞医药): Hengrui is China's largest domestic pharmaceutical company with a broad oncology, autoimmune, and biologic pipeline competing directly with RemeGen in Chinese hospital channels. As the largest incumbent, it anchors the competitive dynamics of NRDL negotiations and hospital tender processes that govern RemeGen's domestic commercial trajectory.

Direct peers

  • BeiGene: BeiGene is a globally commercialized Chinese biotech with BRUKINSA (zanubrutinib) as a flagship hematology asset. It offers a comparable profile of China-origin biologics, A+H/US listings, deep commercial infrastructure in China, and global out-licensing/partnership strategy similar to RemeGen's AbbVie and Vor Bio deals.
  • Akeso (康方生物): Akeso is a Chinese biotech with the PD-1/VEGF bispecific ivonescimab that directly competes with RemeGen's RC148 in non-small cell lung cancer and other oncology indications. Both companies are China-based, platform-driven biologic innovators pursuing global out-licensing deals with similar therapeutic focus areas (oncology/immunology).
  • Innovent Biologics (信达生物): Innovent is a leading Chinese biologics innovator with multiple approved products and PD-1 leadership (sintilimab), pursuing both domestic commercial sales and global BD partnerships. Comparable to RemeGen in therapeutic focus (oncology, autoimmune), biologics platform depth, and commercial model (NRDL-driven hospital sales).
  • Junshi Biosciences (君实生物): Junshi is a Chinese biotech that pioneered PD-1 (toripalimab) and has pursued combination therapies with partners including Coherus. RemeGen's RC48 + toripalimab combination in urothelial carcinoma creates direct clinical collaboration overlap, and Junshi shares RemeGen's A+H dual-listing, biologics platform, and indication-expansion strategy.

Emerging players

  • Cstone Pharmaceuticals (基石药业): Cstone is a smaller Chinese biotech with biologic and bispecific antibody assets pursuing similar out-licensing and indication-expansion strategies. While smaller in scale, it represents a comparable emerging Chinese biologic innovator that competes for global partner interest and KOL mindshare in similar indications.

Market position

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

RemeGen荣昌生物 financial estimates

Financial estimate

Revenue estimate

Valuation estimate

RemeGen荣昌生物 leadership team

Management profile

Number of profiles

Profiles13 records

RemeGen荣昌生物 funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

RemeGen荣昌生物 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 RemeGen荣昌生物

What does RemeGen荣昌生物 do?

RemeGen discovers, develops, manufactures, and commercializes innovative biologic drugs targeting autoimmune diseases, oncology, and ophthalmology. Its commercial portfolio includes Telitacicept (RC18), the world's first BLyS/APRIL dual-target fusion protein biologic, and Disitamab Vedotin (RC48), China's first domestically developed HER2-targeting antibody-drug conjugate (ADC). The company also licenses its pipeline assets to global pharmaceutical partners for international markets.

Is RemeGen荣昌生物 a public or private company?

RemeGen荣昌生物 is a public company. It is classified as public and is currently operating.

When was RemeGen荣昌生物 founded?

RemeGen荣昌生物 was founded in 2008. It employs 1 to 10 people.

Where is RemeGen荣昌生物 based?

RemeGen荣昌生物 is headquartered in Yantai, China, in the Asia region.

How does RemeGen荣昌生物 make money?

Three revenue lines are on record. Domestic Product Sales are the primary driver. The others are BD Licensing/Out-licensing and milestone Payments.

Who are RemeGen荣昌生物's main competitors?

Broad incumbents on record are Daiichi Sankyo, Pfizer, AstraZeneca, Hansoh Pharmaceutical (翰森制药) and Hengrui Pharma (恒瑞医药). Direct peers are BeiGene, Akeso (康方生物), Innovent Biologics (信达生物) and Junshi Biosciences (君实生物). Cstone Pharmaceuticals (基石药业) is listed as an emerging player.

Does RemeGen荣昌生物 have an API?

No public API is recorded for RemeGen荣昌生物.

What industry is RemeGen荣昌生物 in?

RemeGen荣昌生物'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 HLAAAAAB, Recombinant Protein Therapeutics (enzymes, hormones, growth factors). Its NAICS code is 325414 and its SIC code is 2836.

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AInvestRemeGen Co., Ltd. - Entered into SPDB wealth management product agreement no. 11RemeGen Co., Ltd. entered into a wealth management product agreement with Shanghai Pudong Development Bank, designated as agreement no. 11. The agreement was disclosed per financial activity requirements, but specific terms such as amount, duration, and expected returns were not detailed. Investors are advised to monitor subsequent disclosures for further details.36krChina A-Share Pharmaceutical Sector Mid-Term Reporting Season Concludes: Innovative Drug Makers Return to ProfitabilityAs of August 31, 2026, 508 A-share pharmaceutical companies filed semi-annual reports, with 191 showing year-on-year net profit growth and 40 exceeding 100%. Innovative drug makers like RemeGen and CSPC Innovation turned losses into profits, but profit sources vary between BD licensing and product sales. The industry's shift from R&D investment to commercialization realization remains a phased milestone, with sustainability still unverified.PhirdaMNC十亿美元分子开牌倒计时MNCs' Q2 earnings and upcoming clinical trials for potential billion-dollar molecules are reported. Key molecules include BMS's ibetide, Novartis's pelacarsen, and GSK's bepirovirsen, with FDA decisions in August and October. China's innovation is becoming a key growth driver for MNCs.Phirda艾力斯的十倍神话Alices' stock rose nearly tenfold from 12.76 to 138.3 yuan over four years, driven by its EGFR-TKI Fumitinib. The drug's sales grew from 7.9 billion yuan in 2022 to over 50 billion yuan in 2025, with new indications and overseas trials planned. The company faces competition from fourth-generation EGFR-TKIs and patent risks.NejmA Phase 3 Trial of Telitacicept for Systemic Lupus ErythematosusA phase 3 clinical trial conducted in China demonstrated that telitacicept significantly improved clinical response rates in adults with active systemic lupus erythematosus compared to placebo over a 52-week period. The study, funded by RemeGen, reported higher efficacy but also increased incidence of adverse events such as upper respiratory infections and reduced immunoglobulin levels in the treatment group.Stock TitanRemeGen's Telitacicept Shows 98% Response Rate in Phase 3 MG TrialRemeGen announced that 48-week open-label extension data from its China Phase III telitacicept trial for generalized myasthenia gravis will be presented at the 2025 AANEM Annual Meeting. The drug showed a 98.1% response rate in MG-ADL scores, the highest among completed Phase III gMG trials. Vor Bio is advancing the global Phase III trial.DealformaAutoimmune R&D Partnerships and M&A by TechAutoimmune R&D partnerships and M&A activity remained strong in the first half of 2025, with collaborations totaling $14.7 billion and M&A deals reaching $3.2 billion. Major transactions included AbbVie's $2.1 billion acquisition of Capstan and high-value partnerships such as RemeGen-Vor Bio and Syneron Bio-AstraZeneca, driven by biologics, AI-driven discovery, and targeted delivery platforms.PR NewswireRemeGen Announces the Acceptance of the Marketing Application of Telitaccept for the Treatment of Myasthenia Gravis in ChinaRemeGen Co. Ltd. announced that its marketing application for telitacicept to treat generalized myasthenia gravis has been officially accepted by China's Center for Drug Evaluation and included in the priority review process. The drug, which targets B-cell mediated autoimmune responses, follows successful phase III clinical trials completed domestically in August 2024. This acceptance marks a significant regulatory milestone for RemeGen in addressing an unmet medical need for a rare chronic autoimmune disease.