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Company Deals Medical Device PIC

Johnson & Johnson MedTech and CED Medical Sign Third Strategic Cooperation Agreement to Expand Neurointerventional Partnership Behind Qiangyida Stent

Fineline Cube Sep 1, 2026
Company Deals PIC

WestGene and CREATE Sign License Deal to Co‑Develop In Vivo CAR‑T Therapies

Fineline Cube Aug 31, 2026
Company Deals PIC

Simnova Closes nearly RMB 400 Million Series B to Advance CAR‑NK Candidate SNC103

Fineline Cube Aug 31, 2026
Company Deals PIC

Leaderna Therapeutics Closes Series A+ Led by Grand View Capital to Advance Oligonucleotide Pipeline

Fineline Cube Aug 31, 2026
Company Drug PIC

Eli Lilly Wins FDA Approval for Mounjaro Cardiovascular Risk Reduction in Type 2 Diabetes

Fineline Cube Aug 31, 2026
Company Deals Medical Device PIC

Johnson & Johnson MedTech and CED Medical Sign Third Strategic Cooperation Agreement to Expand Neurointerventional Partnership Behind Qiangyida Stent

Fineline Cube Sep 1, 2026
Policy / Regulatory

NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment

Fineline Cube Sep 1, 2026
Company Policy / Regulatory

Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment

Fineline Cube Sep 1, 2026
Company Drug

Johnson & Johnson’s Tremfya Gains FDA Approval for Crohn’s Disease Treatment

Fineline Cube Mar 21, 2025

US pharmaceutical giant Johnson & Johnson (J&J, NYSE: JNJ) has announced receiving clearance from the...

Company Deals

Menarini Group Partners with VisualDx to Enhance BPDCN Identification Using AI/ML Tools

Fineline Cube Mar 21, 2025

Italy’s Menarini Group, through its subsidiary Stemline Therapeutics Inc., has formed a partnership with US-based...

Company Drug

Elevation Oncology Halts EO-3021 Development After Poor Phase 1 Data

Fineline Cube Mar 21, 2025

US-based Elevation Oncology, Inc. (NASDAQ: ELEV) has announced the decision to terminate development of EO-3021...

Company Drug

Changchun High & New Technology Industries Receives US Trial Approval for GenSci120 in Rheumatoid Arthritis

Fineline Cube Mar 21, 2025

China-based Changchun High & New Technology Industries (Group) Inc. (SHE: 000661) announced its subsidiary GenScipt...

Company Drug

Novartis’ Fabhalta Approved by FDA for C3 Glomerulopathy Treatment

Fineline Cube Mar 21, 2025

Swiss pharmaceutical giant Novartis’ (NYSE: NVS) iptacopan, marketed as Fabhalta, has received approval from the...

Company

Sino Biopharmaceutical’s 2024 Revenue Up 10.2% on Strong Innovative Drug Sales

Fineline Cube Mar 21, 2025

China-based Sino Biopharmaceutical Ltd (HKG: 1177) released its 2024 financial report, recording revenues of RMB...

Company Drug

Arcutis Biotherapeutics’ Zoryve Cream Nears FDA Approval for Pediatric Atopic Dermatitis

Fineline Cube Mar 21, 2025

China-based Huadong Medicine Co., Ltd (SHE: 000963) announced that its US partner Arcutis Biotherapeutics, Inc....

Company Deals

Sanofi to Acquire DR-0201 for $600 Million to Advance Myeloid Cell Engager

Fineline Cube Mar 21, 2025

Sanofi (EPA: SAN, NASDAQ: SNY) announced plans to acquire DR-0201, a bispecific myeloid cell engager...

Company Deals

Kexing Biopharm and Hinova Forge Alliance to Expand Global Market Reach

Fineline Cube Mar 21, 2025

China-based Kexing Biopharm Co., Ltd. (SHA: 688136) announced this week a strategic alliance with compatriot...

Company Drug

Kintor Pharmaceutical’s KX-826 Shows Promising Results in Alopecia Phase III Trial

Fineline Cube Mar 21, 2025

China-based Kintor Pharmaceutical Ltd (HKG: 9939) announced positive topline results from the long-term safety Phase...

Company Drug

Junshi Biosciences Receives NMPA Approval for JS212 in Advanced Solid Tumors

Fineline Cube Mar 21, 2025

China-based Shanghai Junshi Biosciences Co., Ltd (HKG: 1877, SHA: 688180) announced receiving clearance from the...

Company Drug

Hengrui’s Trastuzumab Rezetecan Nears 8th Breakthrough Therapy Designation

Fineline Cube Mar 21, 2025

China-based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276) announced that its trastuzumab rezetecan (SHR-A1811), an...

Company Drug

Fosun’s Henlius Receives FDA Orphan Drug Designation for HER2-Targeting HLX22

Fineline Cube Mar 20, 2025

On March 19, 2025, Fosun Pharmaceutical (SHA: 600196) announced that its subsidiary, Henlius, has received...

Company Deals

Paratek Pharmaceuticals to Acquire Optinose for $330 Million

Fineline Cube Mar 20, 2025

Paratek Pharmaceuticals and Optinose, Inc. (NASDAQ: OPTN) announced a definitive merger agreement on March 19,...

Company Deals

Boji Medical’s Huasheng Transfers Glucosamine Sulfate Capsules Technology to Panlong

Fineline Cube Mar 20, 2025

On March 20, 2025, Boji Medical Technology Co., Ltd (known as Boji Biomedicals) (SHE: 300404)...

Company Deals

Oxford BioTherapeutics Partners with Roche on Cancer Therapeutics Discovery

Fineline Cube Mar 20, 2025

On March 19, 2025, Oxford BioTherapeutics announced a multiyear collaboration with Roche (SWX: ROG, OTCMKTS:...

Company Drug

Joyo Pharma’s JYP0035 Receives Clinical Trial Approval for Breast Cancer Treatment

Fineline Cube Mar 20, 2025

On March 14, 2025, Joyo Pharma announced that its independently developed next-generation, highly selective Class...

Policy / Regulatory

CDE Announces 92nd Batch of Reference Preparations for Generic Drug Evaluation

Fineline Cube Mar 20, 2025

China’s Center for Drug Evaluation (CDE) has released the 92nd batch of reference preparations for...

Company

HutchMed’s 2024 Financial Report Shows Dip in Revenue Amid Oncology Product Growth

Fineline Cube Mar 20, 2025

China-based HutchMed (NASDAQ: HCM, HKG: 0013) released its 2024 financial report, revealing a total revenue...

Company Deals

Servier and Black Diamond Therapeutics Ink Global Deal for BDTX-4933

Fineline Cube Mar 20, 2025

French pharmaceutical company Servier and US-based Black Diamond Therapeutics, Inc. (NASDAQ: BDTX) announced a strategic...

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Recent updates

  • NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment
  • Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment
  • Eisai Launches LEQEMBI IQLIK Subcutaneous Auto-Injector for Early Alzheimer’s Disease in the United States
  • Trump Signs Nine New MFN Drug Pricing Agreements, Expanding Pharma Deals to 26 Companies Covering 89% of Branded Market
  • Laekna Doses First Patient in Phase I Study of LAE118 PI3Kα Inhibitor for Advanced Solid Tumors, Licensed to Vasque Bio for Up to USD 527 Million
Special Report 2025 Q1: U.S. Targets Chinese Pharma with 200% Tariffs—Will the Global Drug Market Collapse?

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You Missed

Policy / Regulatory

NMPA CDE Issues Draft Guideline to Reduce or Replace Animal Testing for Monoclonal Antibodies, Opening Public Comment

Company Policy / Regulatory

Shanghai RAAS’s SR604 Enters NMPA CDE Rare Disease Encouragement Program for Hemophilia and Factor VII Deficiency Treatment

Company Drug

Eisai Launches LEQEMBI IQLIK Subcutaneous Auto-Injector for Early Alzheimer’s Disease in the United States

Policy / Regulatory

Trump Signs Nine New MFN Drug Pricing Agreements, Expanding Pharma Deals to 26 Companies Covering 89% of Branded Market

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