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Company Deals

Junshi Biosciences Secures Global Exclusive Rights to CAS’s Tetravalent Recombinant Dengue Vaccine in Landmark Licensing Deal

Fineline Cube Jun 12, 2026
Company Deals

Kelun-Biotech Receives USD 89 Million Settlement Payment from Medilink Therapeutics Over ADC Pipeline Out-Licensing Dispute

Fineline Cube Jun 12, 2026
Company Deals

HJ Science Launches HK$1.11 Billion IPO on Hong Kong Exchange to Advance Clinical-Stage Pipeline in Autoimmune, Metabolic, and Oncology Therapies

Fineline Cube Jun 12, 2026
Company Deals

Cascade Pharmaceuticals Secures RMB 318 Million Series D Financing to Advance Bile Acid Metabolism Pipeline

Fineline Cube Jun 12, 2026
Company Deals

QuantumPharm (XtalPi) Secures $400 Million AI-Driven Partnership for Best-in-Class GPCR-Targeting Oral Small-Molecule Drug

Fineline Cube Jun 11, 2026
Policy / Regulatory

China’s CDE Releases 107th Batch of Reference Preparations for Generic Drug Consistency Evaluation with 17 New Drugs Added

Fineline Cube Jun 12, 2026
Company Drug

Shouyao Holdings Secures NMPA Approval for Second-Generation ALK Inhibitor CT-707 as First-Line Treatment for ALK-Positive NSCLC

Fineline Cube Jun 12, 2026
Company Drug

Createrna’s MY008211A Becomes China’s First Home-Grown Oral CFB Inhibitor Approved for Paroxysmal Nocturnal Hemoglobinuria

Fineline Cube Jun 12, 2026
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...

Company Drug

Simcere Receives NMPA Clearance for SIM0348 Clinical Study

Fineline Cube Dec 30, 2022

China-based Simcere Pharmaceutical Group (HKG: 2096) has announced receiving clearance from the National Medical Products...

Company Deals

Skynor Medical Raises RMB 100 Million in Financing Round for Market Expansion

Fineline Cube Dec 30, 2022

Skynor Medical, a Shanghai-based manufacturer of nerve and peripheral blood vessel implantation and interventional devices,...

Company Deals

Sichuan Kelun Completes RMB 1.5 Billion Financing Round for Kelun-Biotech

Fineline Cube Dec 30, 2022

China-based Sichuan Kelun Pharmaceutical Co., Ltd (SHE: 002422) has announced the completion of a financing...

Company Drug

Everest Medicines’ Nefecon Receives Priority Review Recommendation from CDE

Fineline Cube Dec 30, 2022

China-based Everest Medicines (HKG: 1952) has announced that the Center for Drug Evaluation (CDE) of...

Company Drug

BrightGene Receives NMPA Approval for BGM0504 Clinical Trial

Fineline Cube Dec 30, 2022

China-based BrightGene Bio-Medical Technology Co., Ltd (SHA: 688166) has announced that it has received clinical...

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Recent updates

  • Junshi Biosciences Secures Global Exclusive Rights to CAS’s Tetravalent Recombinant Dengue Vaccine in Landmark Licensing Deal
  • Shouyao Holdings Secures NMPA Approval for Second-Generation ALK Inhibitor CT-707 as First-Line Treatment for ALK-Positive NSCLC
  • Createrna’s MY008211A Becomes China’s First Home-Grown Oral CFB Inhibitor Approved for Paroxysmal Nocturnal Hemoglobinuria
  • China’s CDE Releases 107th Batch of Reference Preparations for Generic Drug Consistency Evaluation with 17 New Drugs Added
  • Takeda’s Zasocitinib Demonstrates Superior Efficacy Over Deucravacitinib in Phase III Psoriasis Trial with 35% PASI 100 Response Rate
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

Junshi Biosciences Secures Global Exclusive Rights to CAS’s Tetravalent Recombinant Dengue Vaccine in Landmark Licensing Deal

Company Drug

Shouyao Holdings Secures NMPA Approval for Second-Generation ALK Inhibitor CT-707 as First-Line Treatment for ALK-Positive NSCLC

Company Drug

Createrna’s MY008211A Becomes China’s First Home-Grown Oral CFB Inhibitor Approved for Paroxysmal Nocturnal Hemoglobinuria

Policy / Regulatory

China’s CDE Releases 107th Batch of Reference Preparations for Generic Drug Consistency Evaluation with 17 New Drugs Added

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