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🇨🇳 China Peptide Market Deep Analysis (2020-2028)

Report ID: MKI-CN-2026-001 | Release Date: July 2026
Coverage: China peptide drugs, API active pharmaceutical ingredients, cosmetic peptides, food peptide market
Data Cutoff: 2026 Q2


1. China Market Overview

China plays a dual role in the global peptide industry chain as an "API production hub + emerging innovative drug R&D market." In 2024, China's therapeutic peptide drug market size was approximately ¥38B (~$5.4B), API exports reached $1.8B, and CDMO service revenue was ¥8.5B.

Core Assessment

China's peptide market is in a transition phase of "generic drug substitution → innovative drug going global." From 2025-2027, domestic GLP-1 drugs will launch intensively, driving accelerated market growth.


2. Market Size and Growth Trajectory

2.1 China Therapeutic Peptide Drug Market Size

Year Market Size (¥B) YoY Growth Key Driving Event
2020 ¥24.5 COVID-19 impacted hospital outpatient volume
2021 ¥26.8 +9.4% Post-VBP peptide generics volume-for-value
2022 ¥29.5 +10.1% GLP-1 prescription volume rapid growth
2023 ¥33.8 +14.6% Semaglutide China sales ¥5.2B
2024 ¥38.0 +12.4% Tirzepatide approved in China, NovoRapid® volume ramp
2025E ¥44.0 +15.8% Mazdutide/Noliglipin expected approval
2026E ¥50.5 +14.8% Multiple domestic GLP-1 launches and ramp
2028E ¥68.0 GLP-1 generics + oral + multi-target drugs

2.2 China Peptide API Market

Year API Market Size (¥B) Export Value ($B) CDMO Revenue (¥B)
2020 ¥7.2 $0.9 ¥3.8
2021 ¥8.4 $1.1 ¥4.5
2022 ¥10.1 $1.3 ¥5.6
2023 ¥11.5 $1.6 ¥7.2
2024 ¥12.8 $1.8 ¥8.5
2025E ¥15.0 $2.2 ¥10.5
2026E ¥17.5 $2.6 ¥12.8

3. Policy Drivers

3.1 "14th Five-Year Plan" Bioeconomy Blueprint

The National Development and Reform Commission's 2022 "14th Five-Year Plan for Bioeconomy Development" explicitly designates peptide drugs as a key bioeconomy development area:

Policy Point Impact
Support peptide innovative drug R&D Included in National Major New Drug Creation Program, R&D funding subsidies up to ¥50M
Encourage API industry upgrade Tax incentives for API manufacturers meeting environmental standards
Promote bio-manufacturing supply chain Suzhou, Nanjing, Hangzhou peptide industry clusters receive policy support
Strengthen international registration certification Support enterprises in obtaining FDA/EMA certification, export tax rebate incentives

3.2 NMPA Review Acceleration

  • From 2023, peptide innovative drugs included in priority review and approval
  • 2024 CDE released "Peptide Drug Pharmaceutical Research Guidelines," clarifying quality requirements
  • Domestic GLP-1 drug review cycle shortened to 6-8 months (historically averaging 18 months)

3.3 Medical Insurance Coverage

Drug Insurance Inclusion Year Pre-Insurance Annual Cost Post-Insurance Out-of-Pocket
Semaglutide Injection 2022 ¥9,600 ¥2,400
Liraglutide Injection 2021 ¥7,200 ¥1,800
Dulaglutide Injection 2023 ¥8,400 ¥2,100
Tirzepatide Injection 2025E ¥12,000 ¥3,000

4.1 Domestic Substitution Progress

China's "import substitution" in the peptide market has moved from early generic drug substitution into a new phase of "innovative drug substitution":

Product Category Import Share (2020) Import Share (2024) Domestic Substitution Leaders
GLP-1 Injectables 95% 70% Renhui Benaglutide, Hansoh PEG-Loxenatide
Anti-Tumor Peptides 60% 45% Domestic leuprolide microspheres, goserelin generics
Cosmetic Peptide Raw Materials 30% 15% Domestic copper peptide, Acetyl Hexapeptide-8
Food Peptide Raw Materials 10% 5% Domestic collagen peptide, soy peptide

4.2 Domestic GLP-1 Pipeline Progress

Company Drug Target Phase Expected Approval
Innovent Biologics Mazdutide GCG/GLP-1 NDA Review 2025 H2
Hengrui Medicine Noliglipin GLP-1 Phase III 2026 H1
Eli Lilly/Innovent GIP/GLP-1 Phase III 2026
Gan & Lee Pharmaceuticals GZR18 GLP-1 Phase III 2026-2027
Changshan Biochemical Ebnbapitide GLP-1 Phase III 2026
Hybio Pharmaceutical Liraglutide Generic GLP-1 Approved 2025 Approved

5. Regional Industrial Clusters

China's peptide industry has formed regional clusters centered on the Yangtze River Delta and Pearl River Delta:

5.1 Major Industrial Clusters

Cluster Representative Companies Core Advantages Global Share
Suzhou WuXi AppTec, Innovent, Shengnuo Biotechnology CDMO concentration, innovative drug R&D Global peptide CDMO 12%
Shanghai Sinopeptide, Huahai Pharma, Hengrui Division R&D headquarters, clinical resources Innovative drug R&D 18%
Shenzhen Hybio, Shenzhen Jianyuan, Snibe API export, device integration Export share 15%
Lianyungang Hansoh Pharma, Chia Tai Tianqing Peptide generic drug production Generics 20%
Hangzhou Hangzhou Jiuyuan Gene, Betta Pharma Innovative drugs, medical devices Emerging cluster
Chengdu/Chongqing Chengdu Shengnuo, Chongqing Lummy Western CDMO capacity Capacity expansion in progress

6. API Export Data Analysis

China's peptide API exports continue to grow and have become a critical link in the global peptide supply chain:

Year Export Value ($B) YoY Growth Main Export Categories
2020 $0.9 Liraglutide, Octreotide API
2021 $1.1 +22% GLP-1 API intermediates
2022 $1.3 +18% Semaglutide API growth significant
2023 $1.6 +23% Semaglutide, Tirzepatide API
2024 $1.8 +13% GLP-1 API accounts for over 40%

6.2 Export Market Distribution

Target Market Export Share Main Products Growth Trend
United States 35% GLP-1 API, intermediates Sustained growth
European Union 28% Generic API, cosmetic peptides Steady growth
India 12% GLP-1 intermediates Rapid growth
Japan/Korea 8% Cosmetic peptides, food peptides Stable
Others 17% Comprehensive Growing

7. Competitive Landscape (Domestic)

7.1 China Peptide Enterprise Revenue Rankings (2024)

Rank Company Peptide Revenue (¥B) Core Products
1 WuXi AppTec (WuXi TIDES) ¥5.8 CDMO services
2 Sinopeptide ¥2.8 GLP-1 API, CDMO
3 Hybio Pharmaceutical ¥2.1 Liraglutide API, injectables
4 Shengnuo Biotechnology ¥1.6 Peptide generics, CDMO
5 Hansoh Pharma ¥1.5 PEG-Loxenatide
6 Asymchem (Kailan Ying) ¥1.2 Peptide CDMO
7 Jiuzhou Pharma ¥0.9 Peptide API

8. Development Outlook (2025-2028)

8.1 Key Assessments

  1. 2025-2026: Domestic GLP-1 innovative drugs (Mazdutide, Noliglipin) approved, opening a new phase in China's GLP-1 market
  2. 2026-2027: GLP-1 generics (liraglutide, semaglutide generics) launch intensively, price decline 30-50%
  3. 2027-2028: Chinese peptide innovative drugs begin going global, first FDA-approved Chinese peptide drug expected
  4. Capacity Continued Expansion: China peptide CDMO capacity to grow from approximately 100,000L in 2024 to 200,000L by 2028

8.2 Risk Factors

Risk Impact Level Description
VBP Price Reduction ★★★★☆ If GLP-1 generics included in VBP, price decline >50%
Environmental Pressure ★★★☆☆ Peptide API production wastewater treatment costs rising
Geopolitics ★★★★☆ US-China relations impacting Chinese API exports
API Quality ★★★☆☆ EPA/DPA impurity standards tightening, export barriers rising

Conclusion

China's peptide market is in a historic growth window. The explosive growth of GLP-1 drugs, the rise of domestic innovative drugs, and the global expansion of CDMO capacity are collectively driving China's market toward the ¥100B milestone. By 2028, China is expected to become the world's largest peptide API supplier and the second-largest consumer market.


Data Sources and Consultation

This report data is sourced from the China Pharmaceutical Industry Information Center, China General Administration of Customs, Yaozhi.com, and various listed company annual reports among other public channels.

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