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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 Deals

Eli Lilly Cancels Licensing Deal for Fosun Pharma’s FCN-338

Fineline Cube Oct 31, 2022

Shanghai Fosun Pharma (Group) Co., Ltd (SHA: 600196, HKG: 2196) announced that its US partner...

Company

Junshi Biosciences Reports 55% Drop in Q3 Revenues

Fineline Cube Oct 31, 2022

Shanghai-based biotech Junshi Biosciences (HKG: 1877) released its financial report for the third quarter of...

Company Deals

Shanghai Duoning Bio Partners with Lisure for Disposable Biopharma System

Fineline Cube Oct 31, 2022

China’s Shanghai Duoning Biotechnology Co., Ltd has entered into a partnership with compatriot firm Lisure...

Company Drug

Santhera and ReveraGen Submit NDA for Vamorolone in Duchenne Muscular Dystrophy

Fineline Cube Oct 31, 2022

Swiss firm Santhera Pharmaceuticals and US-based ReveraGen BioPharma, Inc have announced the rolling submission of...

Policy / Regulatory

Ortho-K Lenses Included in Hebei’s Volume-Based Procurement List

Fineline Cube Oct 30, 2022

The drug and medical device procurement center of Hebei Province released a notification regarding the...

Company Drug

Innovent’s Tyvyt Approved for New Gastric Cancer Indication by NMPA

Fineline Cube Oct 28, 2022

China-based Innovent Biologics, Inc. (HKG: 1801) and its partner Eli Lilly & Co. (NYSE: LLY)...

Company Drug

Zhejiang Huahai Receives FDA ANDA Approval for Generic Tecfidera

Fineline Cube Oct 28, 2022

China-based Zhejiang Huahai Pharmaceutical Co., Ltd (SHA: 600521) announced that it has received Abbreviated New...

Company Deals

Novartis Expands Strategic Collaboration with Bo’Ao Lecheng Pilot Zone

Fineline Cube Oct 28, 2022

Novartis (NYSE: NVS) announced a further strategic collaboration with the Bo’Ao Lecheng Medical Tourism Pilot...

Company Deals

Salubris Partners with Alpha Molecular for AI-Driven Obesity Drug Development

Fineline Cube Oct 28, 2022

China’s Shenzhen Salubris Pharmaceuticals Co., Ltd (SHE: 002294) has entered into a partnership with compatriot...

Company

RemeGen Reports 397.47% YOY Revenue Growth in Q3 2022

Fineline Cube Oct 28, 2022

China-based pharma firm RemeGen (HKG: 9995) released its Q3 2022 financial report, showing significant growth...

Company Drug

Innovent’s Parsaclisib Filed for Marketing Approval in China

Fineline Cube Oct 28, 2022

China’s Center for Drug Evaluation (CDE) has received a marketing approval application for Innovent Biologics...

Company Drug

Proheal Pharmaceuticals Initiates Clinical Study for PHP1003 in Thyroid-Associated Ophthalmopathy

Fineline Cube Oct 28, 2022

Proheal Pharmaceuticals, a Suzhou-based developer of drugs for ophthalmology and autoimmune diseases, announced the first...

Company Drug

HutchMed Initiates Phase II/III Study for Elunate and Tyvyt in Renal Cell Carcinoma

Fineline Cube Oct 28, 2022

China-based Hutchison China Meditech (HutchMed; NASDAQ: HCM, HKG: 0013) announced the initiation of a Phase...

Company

Shanghai Pharmaceuticals Reports 12.86% YOY Revenue Growth in Q3 2022

Fineline Cube Oct 28, 2022

Shanghai Pharmaceuticals (HKG: 2607, SHA: 601607) released its Q3 2022 financial report, recording RMB 62.904...

Company Drug

Recbio’s Neoadjuvant HPV Vaccine Accepted for Review by NMPA

Fineline Cube Oct 28, 2022

China-based vaccine maker Jiangsu Recbio Technology Co., Ltd (HKG: 2179) announced that a clinical trial...

Company Drug

Kintor Completes Enrollment for GT20029 Phase I Study in US

Fineline Cube Oct 28, 2022

China-based Kintor Pharmaceutical Ltd (HKG: 9939) announced the completion of enrollment for a Phase I...

Company Drug

Alphamab Oncology Gains NMPA Approval for JSKN003 Clinical Trial

Fineline Cube Oct 28, 2022

Alphamab Oncology (HKG: 9966) announced that it has received approval from the National Medical Products...

Company Drug

WinHealth’s Ravicti Receives Orphan Drug Designation in Taiwan

Fineline Cube Oct 28, 2022

China-based Hong Kong WinHealth Pharma Group Ltd announced that its Swiss partner Immedica Pharma AB’s...

Company Drug

Lee’s Pharmaceutical’s NVK-002 Shows Strong Results in Phase III CHAMP Study

Fineline Cube Oct 28, 2022

China-based Lee’s Pharmaceutical Holdings Ltd (HKG: 0950) subsidiary Zhaoke Ophthalmology Ltd (HKG: 6622) announced that...

Company Drug

CSPC’s Antibody-Drug Conjugate SYS6002 Gains CDE Approval for Clinical Study

Fineline Cube Oct 28, 2022

China-based CSPC Pharmaceutical Group Co., Ltd (HKG: 1093) announced that it has received approval from...

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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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