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Company Deals

Thermo Fisher Scientific to Divest Microbiology Business to Astorg for $1.075 Billion – Strategic Portfolio Optimization

Fineline Cube Apr 28, 2026
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
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

Santo Therapeutics Secures Dual FDA Designations for ST002 Gene Therapy in NF2-Related Schwannomatosis – Advancing In Vivo Lentiviral Platform

Fineline Cube Apr 28, 2026
Company Drug

Johnson & Johnson’s Imaavy (nipocalimab) Receives FDA Priority Review for Warm Autoimmune Hemolytic Anemia – Expanding FcRn Blocker Franchise

Fineline Cube Apr 28, 2026
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)...

Company Deals

QuantumPharm and Hengjian Launch GBA AI+ Innovation Consortium

Fineline Cube Feb 19, 2025

Shenzhen-based QuantumPharm Inc. (HKG: 2228), also known as Xtalpi Inc., and Guangdong Hengjian Investment Holding...

Company

Deepwise Information Integrates DeepSeek into Medical Data Platform

Fineline Cube Feb 19, 2025

Deepwise Information, a leading artificial intelligence company in the medical field, has fully integrated its...

Company

Weimai Qingtong Medical Technology Completes Tens of Millions Yuan B+ Round

Fineline Cube Feb 19, 2025

Weimai Qingtong Medical Technology (WEMT), a medical device company based in Wuxi, has completed a...

Company Drug

InnoCare Pharma Receives NMPA Approval for Mesutoclax Phase III Study in CLL/SLL

Fineline Cube Feb 18, 2025

Beijing-based biotech InnoCare Pharma (HKG: 9969, SHA: 688428) announced that it has received approval from...

Company Drug

Hengrui Pharma’s HR19034 Eye Drops for Myopia Delay Accepted by NMPA

Fineline Cube Feb 18, 2025

Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276) announced that its market filing for HR19034 eye...

Company Drug

Gan & Lee Pharmaceuticals Doses First Patient in GZR4 Phase III Study for Diabetes

Fineline Cube Feb 18, 2025

China-based Gan & Lee Pharmaceuticals (SHA: 603087) announced that the first patient has been dosed...

Company Deals

Stedical Scientific Raises RMB100M in Series B Financing for Global Expansion

Fineline Cube Feb 18, 2025

Stedical Scientific, a Hangzhou-based tissue engineering and regenerative medicine company, has raised over RMB100 million...

Company Drug

Zelgen Biopharmaceuticals’ ZG005 Bispecific Antibody Receives NMPA Approval for Biliary Tract Cancer Trials

Fineline Cube Feb 18, 2025

China-based Suzhou Zelgen Biopharmaceuticals Co., Ltd (SHA: 688266) announced that it has received clinical trial...

Company Drug

Bristol-Myers Squibb Releases Five-Year Data on Sotyktu’s Long-Term Efficacy and Safety

Fineline Cube Feb 18, 2025

In a recent announcement, US pharmaceutical giant Bristol-Myers Squibb (BMS, NYSE: BMY) unveiled the latest...

Company Drug

Wanbangde New Building Materials’ Mecobalamin Earns FDA Orphan Drug Designation for ALS

Fineline Cube Feb 18, 2025

China’s Wanbangde New Building Materials Co., Ltd (SHE: 002082) announced that its mecobalamin product has...

Company Drug

Biokin Pharmaceutical Registers Phase III Study for BL-B01D1 in EGFR Mutant NSCLC

Fineline Cube Feb 18, 2025

Sichuan Biokin Pharmaceutical Co., Ltd (SHA: 688506) has registered a Phase III study on chinadrugtrials.org.cn...

Company Drug

AccurEdit’s ART002 Becomes First In Vivo Gene Editing Product to Reduce LDL-C in Humans

Fineline Cube Feb 18, 2025

Suzhou-based gene editing specialist AccurEdit Therapeutics announced that its in vivo gene editing product, ART002,...

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Recent updates

  • Santo Therapeutics Secures Dual FDA Designations for ST002 Gene Therapy in NF2-Related Schwannomatosis – Advancing In Vivo Lentiviral Platform
  • Johnson & Johnson’s Imaavy (nipocalimab) Receives FDA Priority Review for Warm Autoimmune Hemolytic Anemia – Expanding FcRn Blocker Franchise
  • AbbVie Submits FDA Filing for Skyrizi Subcutaneous Induction Therapy in Crohn’s Disease – Expanding IL-23 Inhibitor Franchise
  • GSK’s Efimosfermin Receives Dual Regulatory Designations for MASH Treatment – Breakthrough Therapy and PRIME Status Support Phase III Development
  • Prothena’s Coramitug Receives FDA Fast Track Designation for ATTR-CM – Advancing Novo Nordisk’s $1.2B Amyloidosis Pipeline
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

Santo Therapeutics Secures Dual FDA Designations for ST002 Gene Therapy in NF2-Related Schwannomatosis – Advancing In Vivo Lentiviral Platform

Company Drug

Johnson & Johnson’s Imaavy (nipocalimab) Receives FDA Priority Review for Warm Autoimmune Hemolytic Anemia – Expanding FcRn Blocker Franchise

Company Drug

AbbVie Submits FDA Filing for Skyrizi Subcutaneous Induction Therapy in Crohn’s Disease – Expanding IL-23 Inhibitor Franchise

Company Drug

GSK’s Efimosfermin Receives Dual Regulatory Designations for MASH Treatment – Breakthrough Therapy and PRIME Status Support Phase III Development

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