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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 Deals

VectorBuilder Partners with Minaris Regenerative Medicine to Enhance Gene Therapy Solutions

Fineline Cube Mar 13, 2024

VectorBuilder, a specialist in genetic engineering based in China, has entered into a strategic partnership...

Company Drug

Bio-Thera Solutions Gets Green Light for Phase Ib/II Study of ADC BAT8008 in Advanced Solid Tumors

Fineline Cube Mar 13, 2024

Guangzhou-based Bio-Thera Solutions (SHA: 688177) has announced that it has received approval from the National...

Company Drug

Betta Pharmaceuticals’ Ensartinib Accepted for FDA Review for First-Line ALK+ NSCLC Treatment

Fineline Cube Mar 13, 2024

Betta Pharmaceuticals (SHE: 300558), a pharmaceutical company based in China, has announced that the market...

Company Drug

CORXEL Gets CDE Green Light for Phase III Aficamten Study in nHCM

Fineline Cube Mar 13, 2024

CORXEL, formerly known as Ji Xing Pharmaceuticals, a China-based pharmaceutical company, has announced that it...

Company Drug

InnoCare Pharma Receives IND Approval in China for BCL2 Inhibitor Combo Therapy

Fineline Cube Mar 13, 2024

InnoCare Pharma (HKG: 9969; SHA: 688428), a Beijing-based biotech company, has announced that it has...

Company Drug

Simcere Pharmaceutical Gets NMPA Approval for Clinical Study of Trispecific Antibody SIM0500

Fineline Cube Mar 13, 2024

Simcere Pharmaceutical Group (HKG: 2096), a biopharmaceutical company based in China, has announced that it...

Company Drug

Fosun Pharmaceutical Gets NMPA Green Light for Phase I Study of Fibrosis Drug HLX6018

Fineline Cube Mar 13, 2024

Shanghai Fosun Pharmaceutical (Group) Co., Ltd (SHA: 600196, HKG: 2196), a leading pharmaceutical company based...

Policy / Regulatory

NMPA Releases 78th Batch of Reference Drugs for Generic Quality Consistency Evaluation

Fineline Cube Mar 13, 2024

The National Medical Products Administration (NMPA) has released the 78th batch of reference drugs for...

Policy / Regulatory

China’s NHC Outlines Cross-departmental Law Enforcement to Strengthen Medical Supervision

Fineline Cube Mar 13, 2024

The National Health Commission (NHC) has issued a set of “Opinions on Strengthening Cross-departmental Law...

Company Deals

Kexing Pharmaceutical Secures Rights for Chia Tai Tianqing’s Generic Ibrance in 11 Countries

Fineline Cube Mar 12, 2024

Kexing Pharmaceutical (SHA: 688136), based in China, has entered into an international collaboration agreement with...

Company Drug

Kelun-Biotech’s A400 Receives Fast-Track Status from FDA for RET Fusion-Positive NSCLC

Fineline Cube Mar 12, 2024

Sichuan Kelun Pharmaceutical Co., Ltd (SHE: 002422) announced that its innovative drug development subsidiary, Sichuan...

Company Drug

Sinocelltech Gains NMPA Approval for Clinical Study of SCTB35 in B-Cell Non-Hodgkin’s Lymphoma

Fineline Cube Mar 12, 2024

Sinocelltech Group Ltd (SHA: 688520), based in China, has announced that it has received clearance...

Company Drug

Huadong Medicine Secures NMPA Approval for HDM1005, Targeting Type 2 Diabetes and Obesity

Fineline Cube Mar 12, 2024

Huadong Medicine Co., Ltd (SHE: 000963), based in China, has announced that it has received...

Company Drug

Innovent and HutchMed’s Combination Therapy Set for Priority Review in China for Advanced Endometrial Cancer

Fineline Cube Mar 12, 2024

China’s Center for Drug Evaluation (CDE) has indicated that the combination therapy of Innovent Biologics...

Company Drug

Sanofi’s Amlitelimab Shows Promising Phase IIb Results in Atopic Dermatitis, Potential for 12-Week Dosing

Fineline Cube Mar 12, 2024

Sanofi (NASDAQ: SNY) announced this week promising results from a Phase IIb study of its...

Company Deals

Jiangsu QYuns Therapeutics Eyes HK IPO to Raise Up to HKD 243 Million for Autoimmune Pipeline

Fineline Cube Mar 12, 2024

Jiangsu QYuns Therapeutics Co., Ltd. (HKG: 2509), based in China, is poised to launch an...

Company

Legend Biotech Reports Q4 and Full-Year 2023 Financials with Focus on Carvykti Milestones

Fineline Cube Mar 12, 2024

Legend Biotech Corporation (NASDAQ: LEGN) has released its financial results for the fourth quarter and...

Company Deals

Gilead Nears Completion of CymaBay Acquisition After Waiting Period Expires

Fineline Cube Mar 12, 2024

Gilead Sciences (NASDAQ: GILD) has moved one step closer to finalizing its cash tender offer...

Company Drug

J&J’s Tremfya Files for Ulcerative Colitis Indication with FDA, Building on Positive Late-Stage Data

Fineline Cube Mar 12, 2024

The US Food and Drug Administration (FDA) has accepted an indication extension filing from Johnson...

Company Drug

Simcere Secures FDA Approval for Clinical Study of Trispecific Antibody SIM0500 in Multiple Myeloma

Fineline Cube Mar 11, 2024

Simcere Pharmaceutical Group (HKG: 2096), based in China, has received approval from the U.S. Food...

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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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