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Company Drug PIC

Allergan Aesthetics’ SKINVIVE by Juvéderm Wins NMPA Approval for Perioral Wrinkles, Backed by 93.4% POLSS Responder Rate

Fineline Cube Sep 2, 2026
Company Deals PIC

Simcere Zaiming Licenses SIM0660 Trispecific Antibody to Roche in Up to USD 1.53 Billion Oncology Deal

Fineline Cube Sep 2, 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
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 Drug PIC

Allergan Aesthetics’ SKINVIVE by Juvéderm Wins NMPA Approval for Perioral Wrinkles, Backed by 93.4% POLSS Responder Rate

Fineline Cube Sep 2, 2026
Policy / Regulatory

NHSA Releases Version 3.0 DRG and DIP Grouping Schemes, Setting 2027 Deadline for China’s Disease-Based Payment Overhaul

Fineline Cube Sep 2, 2026
Company Drug

GSK mRNA Influenza Vaccine Candidate Shows Superior Immune Responses in Phase II Versus Licensed Flu Shots

Fineline Cube Sep 2, 2026
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...

Company Drug

Hengrui Pharma Secures NMPA Approval for HRS‑7172 Targeting RAS‑Mutated Tumors

Fineline Cube Sep 3, 2025

China‑based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (HKG: 1276, SHA: 600276) today announced that its novel...

Company Drug

MSD Reports Positive Phase 3 CORALreef Lipids Results for Oral PCSK9 Inhibitor Enlicitide

Fineline Cube Sep 3, 2025

US-based Merck, Sharp & Dohme Inc. (MSD; NYSE: MRK) disclosed encouraging topline results from the...

Company Deals Drug

OMass Therapeutics Teams Up with Genentech on First‑in‑Class IBD Oral Small Molecule

Fineline Cube Sep 3, 2025

OMass Therapeutics, a biotechnology firm that discovers medicines targeting membrane proteins and intracellular complexes, has...

Company Deals

Arrowhead Partners with Novartis for ARO‑SNCA siRNA Therapy

Fineline Cube Sep 3, 2025

Arrowhead Pharmaceuticals, Inc. (NASDAQ: ARWR) today unveiled a worldwide licensing and collaboration agreement with Novartis...

Company Deals

Novatim Licenses KY‑0301 Nano‑Bispecific ADC to RADIANCE Biopharma

Fineline Cube Sep 2, 2025

Novatim Immune Therapeutics (Zhejiang) Co., Ltd. announced a landmark exclusive licensing collaboration with RADIANCE Biopharma....

Company Drug

Zai Lab’s TIVDAK Wins Hong Kong Approval for Recurrent Cervical Cancer

Fineline Cube Sep 2, 2025

China-based biotech Zai Lab Limited (NASDAQ: ZLAB, HKG: 9688) has secured a pivotal regulatory milestone:...

Company Drug

Fosun Launches Futuoning, First‑In‑Class CDK4/6 Inhibitor for HR‑Positive Breast Cancer

Fineline Cube Sep 2, 2025

Shanghai Fosun Pharmaceutical (Group) Co., Ltd. (HKG: 2196, SHA: 600196) announced the nationwide launch of...

Company Drug

Fosun Secures FDA Approval for Two Denosumab Biosimilar Formulations

Fineline Cube Sep 2, 2025

Shanghai Fosun Pharmaceutical (Group) Co., Ltd. (HKG: 2196, SHA: 600196) announced that the Biologics License...

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Recent updates

  • NHSA Releases Version 3.0 DRG and DIP Grouping Schemes, Setting 2027 Deadline for China’s Disease-Based Payment Overhaul
  • GSK mRNA Influenza Vaccine Candidate Shows Superior Immune Responses in Phase II Versus Licensed Flu Shots
  • NMPA Tightens Drug Traceability Rules, Mandating Full-Chain Code Scanning for MAHs and Distributors
  • Allergan Aesthetics’ SKINVIVE by Juvéderm Wins NMPA Approval for Perioral Wrinkles, Backed by 93.4% POLSS Responder Rate
  • Beijing Huasu Wins NMPA Clinical Trial Approval for Methylphenidate ER Chewable Tablets, First Domestic Generic for ADHD Treatment
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

NHSA Releases Version 3.0 DRG and DIP Grouping Schemes, Setting 2027 Deadline for China’s Disease-Based Payment Overhaul

Company Drug

GSK mRNA Influenza Vaccine Candidate Shows Superior Immune Responses in Phase II Versus Licensed Flu Shots

Policy / Regulatory

NMPA Tightens Drug Traceability Rules, Mandating Full-Chain Code Scanning for MAHs and Distributors

Company Drug PIC

Allergan Aesthetics’ SKINVIVE by Juvéderm Wins NMPA Approval for Perioral Wrinkles, Backed by 93.4% POLSS Responder Rate

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