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Company Deals

Aureka Biotechnologies Secures $35M Series A+ Financing to Advance AuraIDE Platform for Functional Antibody Design

Fineline Cube Apr 28, 2026
Company Deals

Hangzhou’s Adcoris Licenses First-in-Class 5T4-Targeting ADC ACR246 to U.S. Biotech K2 Therapeutics in Deal Worth Up to $730 Million

Fineline Cube Apr 27, 2026
Company Deals

Sino Biopharmaceutical’s Chia Tai Tianqing and Shanghai Reunion Partner to Commercialize Respacio Hydrogel for Cervical Cancer Radiotherapy Protection in China

Fineline Cube Apr 27, 2026
Company Deals

Beijing QL Biopharma Files HKEX IPO Prospectus with Diversified GLP-1 Portfolio Targeting Global Obesity and Metabolic Disease Markets

Fineline Cube Apr 27, 2026
Company Deals

China Resources Double-Crane to Acquire Nanjing Xinbai Pharma from Boya Biological for RMB 235.5 Million, Expanding Injectables Portfolio

Fineline Cube Apr 27, 2026
Policy / Regulatory

NMPA Tightens Post-Marketing Requirements for Conditionally Approved Drugs in China, Mandating Four-Year Confirmatory Studies and Annual Progress Reporting

Fineline Cube Apr 27, 2026
Company Drug

BeBetter Medicine Secures FDA Clearance for BEBT-701 Clinical Study – First-in-Class Dual-Target Therapy for Hypertension and High LDL-C

Fineline Cube Apr 28, 2026
Company Drug

Hinova Pharmaceuticals Reports Positive Phase IIa Results for HP515 in MASH Treatment – First THR-β Agonist Candidate in China

Fineline Cube Apr 28, 2026
Company Drug

Junshi Biosciences’ CGRP Monoclonal Antibody JS010 Accepted for NMPA Review

Fineline Cube Jan 3, 2023

China-based Junshi Biosciences (HKG: 1877, SHA: 688180) has announced that the clinical trial filing for...

Company Drug

BeiGene’s Tislelizumab Receives NMPA Review for First-Line HCC Indication

Fineline Cube Jan 3, 2023

BeiGene (HKG: 6160, SHA: 688235, NASDAQ: BGNE) has revealed that a supplementary Biologic License Application...

Company Deals

Immunohead Biotech Raises RMB 200 Million in Series A+ Financing Round

Fineline Cube Jan 3, 2023

Immunohead Biotechnology Co., Ltd, a cell therapy developer based in Suzhou, has reportedly raised close...

Company Deals

Biocytogen and Hansoh Enter Antibody Collaboration and Licensing Agreement

Fineline Cube Jan 3, 2023

China-based Biocytogen Pharmaceuticals (Beijing) Co., Ltd has announced an antibody collaboration, assignment, and exclusive license...

Company Drug

CStone Pharmaceuticals Achieves Primary Endpoint in GEMSTONE-304 Study for Sugemalimab

Fineline Cube Jan 3, 2023

China-based CStone Pharmaceuticals (HKG: 2616) has announced the achievement of the primary endpoint in the...

Company Drug

3D Medicines Gains FDA Approval for Phase II Study of Envafolimab in dMMR Tumors

Fineline Cube Jan 3, 2023

China-based oncology specialist 3D Medicines (HKG: 1244) has announced receiving approval from the US FDA...

Company Drug

Changzhou Qianhong Completes Phase I Study of QHRD107 for Acute Myeloid Leukemia

Fineline Cube Jan 3, 2023

China-based Changzhou Qianhong Bio-pharma Co., Ltd (SHE: 002550) has announced the completion of enrollment and...

Company Drug Hospital

Guangdong Zhongsheng Completes Enrollment for RAY1216 Phase III Study in COVID-19

Fineline Cube Jan 3, 2023

China – based Guangdong Zhongsheng Pharmaceutical Co., Ltd (SHE: 002317) has announced the completion of...

Drug Policy / Regulatory

CDE Releases 65th Batch of Chemical Generic Reference Preparations

Fineline Cube Jan 3, 2023

The Center for Drug Evaluation (CDE) has released the 65th batch of chemical generic reference...

Company Drug Legal / IP

Viking Therapeutics Sues Ascletis Pharma Over Alleged Trade Secret Theft

Fineline Cube Jan 3, 2023

US – based Viking Therapeutics (NASDAQ: VKTX) is set to take China’s Ascletis Pharma Inc....

Company Deals

Shuwen Biotech Partners with Nottingham University Hospitals for MammaTyper

Fineline Cube Jan 3, 2023

China – based diagnostic specialist Shuwen Biotech Co., Ltd and its German wholly – owned...

Company Drug

Chinagene Tech’s ZVS101e Receives FDA IND Approval for Bietti’s Crystalline Dystrophy

Fineline Cube Jan 3, 2023

Beijing – based Chinagene Tech, a specialist in hereditary ophthalmopathy diagnosis and gene therapy, has...

Drug Policy / Regulatory

Jiangxi Leads 16-Province VBP Alliance with Winning Bids Announced

Fineline Cube Jan 3, 2023

The Jiangxi Province Healthcare Security Administration has released a notification regarding the winning bids of...

Company Medical Device

NMPA Approves 172 Medical Devices for Marketing in November 2022

Fineline Cube Dec 30, 2022

The National Medical Products Administration (NMPA) approved 172 medical devices for marketing in November 2022....

Company Drug

Merck’s Lagevrio Receives Emergency Conditional Approval from China’s NMPA

Fineline Cube Dec 30, 2022

US-based Merck, Sharp & Dohme Inc. (MSD; NYSE: MRK) has announced receiving emergency conditional approval...

Policy / Regulatory

NHSA and CNIPA Issue Opinions on Strengthening IP Protection in Drug Procurement

Fineline Cube Dec 30, 2022

The National Healthcare Security Administration (NHSA) and the China National Intellectual Property Administration (CNIPA) have...

Company Drug

Legend Biotech’s Carvykti Accepted for Review by China’s CDE

Fineline Cube Dec 30, 2022

The Center for Drug Evaluation (CDE) website indicates that a market approval filing from Legend...

Company Deals

F-star Therapeutics and Sino Biopharmaceutical Face Delays in Proposed Acquisition

Fineline Cube Dec 30, 2022

UK-based biotech F-star Therapeutics (NASDAQ: FSTX) released an SEC filing indicating that the proposed acquisition...

Company Drug

CSPC’s ALMB-0168 Receives NMPA Approval for Osteoarthritis Clinical Study

Fineline Cube Dec 30, 2022

China-based CSPC Pharmaceutical Group Ltd (HKG: 1093) has announced receiving approval from the National Medical...

Company Drug

RemeGen’s RC108 Receives FDA Go-Ahead for Phase I Clinical Study

Fineline Cube Dec 30, 2022

China-based biopharma RemeGen Ltd (HKG: 9995) has announced receiving approval from the US FDA to...

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Recent updates

  • Aureka Biotechnologies Secures $35M Series A+ Financing to Advance AuraIDE Platform for Functional Antibody Design
  • BeBetter Medicine Secures FDA Clearance for BEBT-701 Clinical Study – First-in-Class Dual-Target Therapy for Hypertension and High LDL-C
  • Hinova Pharmaceuticals Reports Positive Phase IIa Results for HP515 in MASH Treatment – First THR-β Agonist Candidate in China
  • Bio-Thera Solutions Reports 25.84% Revenue Growth in 2025 Driven by Biosimilar Portfolio Expansion and US Market Entry
  • Hangzhou’s Adcoris Licenses First-in-Class 5T4-Targeting ADC ACR246 to U.S. Biotech K2 Therapeutics in Deal Worth Up to $730 Million
Special Report 2025 Q1: U.S. Targets Chinese Pharma with 200% Tariffs—Will the Global Drug Market Collapse?

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You Missed

Company Deals

Aureka Biotechnologies Secures $35M Series A+ Financing to Advance AuraIDE Platform for Functional Antibody Design

Company Drug

BeBetter Medicine Secures FDA Clearance for BEBT-701 Clinical Study – First-in-Class Dual-Target Therapy for Hypertension and High LDL-C

Company Drug

Hinova Pharmaceuticals Reports Positive Phase IIa Results for HP515 in MASH Treatment – First THR-β Agonist Candidate in China

Others

Bio-Thera Solutions Reports 25.84% Revenue Growth in 2025 Driven by Biosimilar Portfolio Expansion and US Market Entry

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