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Company Deals

CureGene Pharmaceutical Secures RMB 300 Million Series C to Advance Global Clinical Pipeline

Fineline Cube May 9, 2026
Company Deals

Hengrui Pharmaceuticals Expands Greater Bay Area Presence with Hong Kong Office Launch and Cancer Foundation Partnership

Fineline Cube May 9, 2026
Company Deals

Fosun Pharma Secures Exclusive China Rights to InxMed’s FAK Inhibitors for Solid Tumor Treatment

Fineline Cube May 9, 2026
Company Deals

Harbour BioMed Joins $165M Cross Financing Round for Windward Bio to Advance Ultra-Long-Acting TSLP Immunotherapies

Fineline Cube May 8, 2026
Company Deals

Roche Acquires PathAI for $750M to Accelerate Digital Pathology and AI-Driven Diagnostic Transformation

Fineline Cube May 8, 2026
Policy / Regulatory

NHSA Launches 2026 NRDL Adjustment with Expanded Eligibility Criteria and Revised Weight Standards

Fineline Cube May 11, 2026
Company Drug

Hansoh Pharmaceutical’s B7-H3 ADC HS-20093 Receives Fifth NMPA Breakthrough Therapy Designation for Esophageal Cancer

Fineline Cube May 11, 2026
Company Drug

CStone Pharmaceuticals Launches First Commercial Batch of Gavreto in China Following NRDL Inclusion

Fineline Cube May 11, 2026
Company Drug

Hepalink Pharmaceutical’s H1710 Heparanase Inhibitor Approved for Phase I Study

Fineline Cube Feb 20, 2025

China-based Shenzhen Hepalink Pharmaceutical Group Co., Ltd (SHE: 002399) announced that it has received approval...

Company Drug

Henlius Biotech’s Avastin Biosimilar Hanbeitai Approved in Bolivia

Fineline Cube Feb 20, 2025

Shanghai Henlius Biotech Inc. (HKG: 2696) announced that its biosimilar of Roche’s Avastin (bevacizumab), Hanbeitai,...

Company Drug

Astellas Pharma’s Xospata Wins Regular NMPA Approval for FLT3-Mutated AML

Fineline Cube Feb 20, 2025

Japan-based Astellas Pharma Inc. (TYO: 4503, OTCMKTS: ALPMY ) announced that the National Medical Products...

Company Drug

Hanx Biopharmaceuticals’ HX009 Receives NMPA Clearance for TNBC Study

Fineline Cube Feb 20, 2025

Hanx Biopharmaceuticals (Wuhan) Co., Ltd. announced that it has received clearance from the National Medical...

Company Medical Device

Huadong Medicine’s MediBeacon TGFR System Approved by NMPA for GFR Measurement

Fineline Cube Feb 20, 2025

China-based Huadong Medicine Co., Ltd (SHE: 000963) announced that it has received marketing approval from...

Company Deals

Sunshine Guojian and Shenyang 3SBio License 612 and 708 Programs for Anti-Tumor Development

Fineline Cube Feb 20, 2025

China-based Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd and Shenyang 3SBio Co., Ltd, both subsidiaries of...

Company

Antengene to Boost T Cell Engager Platform with AI Investment and DeepSeek Deployment

Fineline Cube Feb 20, 2025

China-based biopharma Antengene Corp., Ltd (HKG: 6996) announced plans to increase investment in establishing a...

Company Deals

Jiangxi Rimag Group and Xunfei Healthcare Form Strategic Alliance for Smart Healthcare

Fineline Cube Feb 20, 2025

China-based Jiangxi Rimag Group Co., Ltd (HKG: 2522) announced a strategic alliance with Xunfei Healthcare...

Company Deals

Rendu Biotechnology Partners with Green Apple Medical System for RNA Diagnostics Expansion

Fineline Cube Feb 20, 2025

Rendu Biotechnology Co., Ltd., (SHA: 688193) a Shanghai-based specialist in RNA molecular diagnostics, has entered...

Company Deals

Genuine Biotech Files for Hong Kong IPO with Azvudine and ZS-1003 in Pipeline

Fineline Cube Feb 20, 2025

China-based Genuine Biotech Limited has filed for an initial public offering (IPO) on the Hong...

Company Legal / IP

AstraZeneca Faces Class Action Lawsuits Over China Legal Issues

Fineline Cube Feb 20, 2025

AstraZeneca plc (AZ, NASDAQ: AZN) is facing multiple class action lawsuits in the United States...

Company Deals Drug

Biogen Licenses Stoke Therapeutics’ Zorevunersen for Dravet Syndrome Outside Americas

Fineline Cube Feb 19, 2025

US-based Biogen Inc. (NASDAQ: BIIB) has entered into a licensing agreement with Stoke Therapeutics, Inc....

Company Drug

TAHO Pharma’s TAH3311 Oral Film Shows Bioequivalence to Eliquis in Study

Fineline Cube Feb 19, 2025

Taiwan-based TAHO Pharmaceuticals announced positive preliminary results from a pivotal study for its TAH3311 oral...

Company Drug

Sanofi’s Dupixent Receives Priority Review from FDA for Bullous Pemphigoid Treatment

Fineline Cube Feb 19, 2025

Sanofi (EPA: SAN, NASDAQ: SNY) announced that the US Food and Drug Administration (FDA) has...

Company Deals

CSPC Pharma Licenses SYS 6005 to Radiance Biopharma for Global Markets

Fineline Cube Feb 19, 2025

China-based CSPC Pharmaceutical Group Ltd (HKG: 1093) announced a licensing agreement with Radiance Biopharma, Inc.,...

Company Drug

Biokin Pharmaceutical’s BL-M07D1 Receives NMPA Approval for Phase II/III Study in HER2+ Breast Cancer

Fineline Cube Feb 19, 2025

China-based Sichuan Biokin Pharmaceutical Co., Ltd (SHA: 688506) announced that it has received approval from...

Company Drug

Gilead Sciences’ Lenacapavir NDA for HIV Prevention Accepted by FDA for Priority Review

Fineline Cube Feb 19, 2025

US-based Gilead Sciences Inc. (NASDAQ: GILD) announced that the New Drug Application (NDA) for its...

Company Drug

Merck’s Welireg Wins Conditional EU Approval for VHL Disease and Advanced RCC

Fineline Cube Feb 19, 2025

US pharmaceutical giant Merck, Sharp & Dohme (MSD, NYSE: MRK) announced that it has received...

Company

GSK and Abbott Announce Leadership Changes in Key Roles

Fineline Cube Feb 19, 2025

Recent days have seen significant leadership changes at two pharmaceutical giants: UK-based GSK plc (LON:...

Company

Medtronic Q3 Earnings Show 4.1% Organic Growth, Driven by Cardiac Ablation

Fineline Cube Feb 19, 2025

US-Irish medical device company Medtronic (NYSE: MDT) reported financial results for the third quarter (Q3)...

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Recent updates

  • Hansoh Pharmaceutical’s B7-H3 ADC HS-20093 Receives Fifth NMPA Breakthrough Therapy Designation for Esophageal Cancer
  • CStone Pharmaceuticals Launches First Commercial Batch of Gavreto in China Following NRDL Inclusion
  • NHSA Launches 2026 NRDL Adjustment with Expanded Eligibility Criteria and Revised Weight Standards
  • Wenda Pharmaceutical Secures NMPA Breakthrough Therapy Designation for NHWD-870 in Rare NUT Carcinoma
  • European Commission Approves Bristol Myers Squibb’s Sotyktu for Psoriatic Arthritis Following FDA Clearance
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 Drug

Hansoh Pharmaceutical’s B7-H3 ADC HS-20093 Receives Fifth NMPA Breakthrough Therapy Designation for Esophageal Cancer

Company Drug

CStone Pharmaceuticals Launches First Commercial Batch of Gavreto in China Following NRDL Inclusion

Policy / Regulatory

NHSA Launches 2026 NRDL Adjustment with Expanded Eligibility Criteria and Revised Weight Standards

Company Drug

Wenda Pharmaceutical Secures NMPA Breakthrough Therapy Designation for NHWD-870 in Rare NUT Carcinoma

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