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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 Drug

Hengrui’s SHR‑A2009 ADC Gains NMPA Approval for HER3‑Targeted Tumor Therapy

Fineline Cube Sep 4, 2025

China‑based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (HKG: 1276, SHA: 600276) announced that the China National Medical...

Company Drug

Haisco Pharmaceutical’s HSK47388 Gears Up for New Autoimmune Trial – NMPA Approval

Fineline Cube Sep 4, 2025

Haisco Pharmaceutical Group Co., Ltd. (SHE: 002653) announced that the National Medical Products Administration (NMPA)...

Company Drug

Boji Medical’s FCZR Approved for Otomycosis Trials – First Liquid Eardrop in China

Fineline Cube Sep 4, 2025

Boji Medical Technology Co., Ltd. (SHE: 300404) has secured approval from the National Medical Products...

Company Drug

Hengrui’s HRS9531 Injection Clears NMPA Approval, Hits 19.2% Weight Loss in Phase 3

Fineline Cube Sep 4, 2025

China‑based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (HKG: 1276, SHA: 600276) confirmed that China’s National Medical Products...

Company Deals Drug

Biocytogen, Merck Partner on Antibody‑Conjugated Lipid Nanoparticles

Fineline Cube Sep 4, 2025

China’s Biocytogen Pharmaceuticals (Beijing) Co., Ltd. (HKG: 2315) announced that it has signed an evaluation...

Company Deals

Argo Biopharma, Novartis Expand siRNA Collaboration for Cardiovascular Drugs

Fineline Cube Sep 4, 2025

Argo Biopharma, a Shanghai‑based siRNA drug developer, announced a new strategic cooperation agreement with Novartis...

Company Deals

ChemPartner & Toposcend Form $200 M Healthcare Fund to Back Innovative Drugs

Fineline Cube Sep 4, 2025

ChemPartner Pharmatech Co., Ltd. (SHE: 300149) announced that its wholly‑owned subsidiary, Beihai ChemPartner Venture Capital...

Company Drug

AbbVie Secures NMPA Priority Review for Epcoritamab in Relapsed Follicular Lymphoma

Fineline Cube Sep 4, 2025

American pharmaceutical giant AbbVie (NYSE: ABBV) disclosed that its bispecific T‑cell engager, epcoritamab, has been...

Company Deals

Replicate Bioscience Teams With Novo Nordisk On srRNA‑Powered Metabolic Drugs

Fineline Cube Sep 4, 2025

Replicate Bioscience, a pioneer in self‑replicating RNA (srRNA) therapeutics, announced a landmark multi‑year research partnership...

Company Drug

Simcere Secures NMPA Approval for Deunoxavir Marboxil, First Pediatric Influenza Drug

Fineline Cube Sep 4, 2025

Simcere Pharmaceutical Group Limited (HKG: 2096) today announced that the National Medical Products Administration (NMPA)...

Policy / Regulatory

FDA Unveils RDEP to Accelerate Rare Disease Therapy Development

Fineline Cube Sep 4, 2025

The U.S. Food and Drug Administration (FDA) today issued the Rare Disease Evidence Principles (RDEP),...

Company Drug

Aosaikang Launches Phase III Trial of ASK202 with Leatinib for NSCLC

Fineline Cube Sep 4, 2025

China’s Beijing Aosaikang Pharmaceutical Co., Ltd. (SHE: 002755) announced today that the first patient has...

Company Drug

Ab&B Bio‑Tech Wins NMPA Approval for First‑Ever Quadrivalent Influenza Subunit Vaccine

Fineline Cube Sep 4, 2025

Ab&B Bio‑Tech CO., LTD. JS (HKG: 2627) disclosed that its quadrivalent influenza virus subunit vaccine...

Company Drug

Sanofi’s Tzield Earns China NMPA Approval for Stage 2 Type 1 Diabetes

Fineline Cube Sep 4, 2025

French pharmaceutical giant Sanofi (NASDAQ: SNY) today announced that its investigational drug Tzield (teplizumab) has...

Company Deals

Zenas Secures $300 M Royalty Deal for Obexelimab – Royalty Pharma to Invest

Fineline Cube Sep 4, 2025

Zenas BioPharma, Inc. (NASDAQ: ZBIO) and Royalty Pharma, Inc. (NASDAQ: RPRX) announced a milestone partnership...

Company Deals

Enlaza‑Vertex Partner on $45 M Multi‑Target Drug Discovery Collaboration

Fineline Cube Sep 3, 2025

Enlaza Therapeutics, Inc. and Vertex Pharmaceuticals, Inc. (NASDAQ: VRTX) today announced a multi‑target drug discovery...

Company Deals

Servier Secures Global Rights to Darovasertib for Uveal Melanoma Treatment

Fineline Cube Sep 3, 2025

French firm Servier Pharmaceutical plc. and IDEAYA Biosciences Inc. (NASDAQ: IDYA) announced an exclusive licensing...

Company Drug

JT118 Vaccine Receives NMPA Approval for Monkeypox Prevention

Fineline Cube Sep 3, 2025

Shanghai Junshi Biosciences Co., Ltd. (HKG: 1877, SHA: 688180) announced that China’s National Medical Products...

Company Drug

Pfizer‑BioNTech Receives FDA Approval for New COVID‑19 Vaccine Indication for High‑Risk Adults

Fineline Cube Sep 3, 2025

Pfizer Inc. (NYSE: PFE) and BioNTech SE (NASDAQ: BNTX) today announced that the United States...

Policy / Regulatory

NMPA Adds 35 New Reference‑Listed Drugs to 95th Catalog, Updates 31 Existing Specs

Fineline Cube Sep 3, 2025

The National Medical Products Administration (NMPA) today announced the release of its 95th Reference‑Listed Drugs...

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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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