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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

Hengrui Pharmaceuticals Reports 15.88% Revenue Growth in 2025 Semi-Annual Results

Fineline Cube Aug 22, 2025

Jiangsu Hengrui Pharmaceuticals Co., Ltd. (HKG: 1276, SHA: 600276) has released its 2025 semi-annual report, highlighting...

Policy / Regulatory

China’s NMPA Resumes Import of Vasudha’s Loratadine API After Rectifications

Fineline Cube Aug 22, 2025

China’s National Medical Products Administration (NMPA) announced on August 20, 2025, that it had resumed...

Company Deals Drug

Jazz Pharmaceuticals Secures Global Rights to Saniona’s Epilepsy Drug SAN2355

Fineline Cube Aug 22, 2025

Jazz Pharmaceuticals plc (NASDAQ: JAZZ) and Saniona (STO: SANION) announced today that they have entered...

Company Deals

Kite Pharma Acquires Interius BioTherapeutics for $350 Million to Boost CAR Therapy Platform

Fineline Cube Aug 22, 2025

On August 22, 2025, Kite Pharma, Inc., a subsidiary of Gilead Sciences (NASDAQ: GILD), announced...

Company Drug

Ionis Pharmaceuticals’ DAWNZERA Approved by FDA for HAE Prevention

Fineline Cube Aug 22, 2025

Ionis Pharmaceuticals, Inc. (NASDAQ: IONS) announced on August 22, 2025, that the U.S. Food and...

Company Drug Policy / Regulatory

InnoCare Pharma’s ICP-723 Joins China’s SPARK Project for Pediatric Solid Tumors

Fineline Cube Aug 22, 2025

China’s Center for Drug Evaluation (CDE) under the National Medical Products Administration (NMPA) has announced...

Company Medical Device

Lifetech Scientific’s PDA Occluder Gains NMPA Innovative Device Review Status

Fineline Cube Aug 22, 2025

On August 22, 2025, China-based Lifetech Scientific Corporation (HKG: 1302) announced that its nitinol patent...

Company Deals

Bio-Thera Inks EUR 136m Deal with STADA for BAT1806 Commercialization

Fineline Cube Aug 21, 2025

On August 21, 2025, Bio-Thera Solutions, Ltd. (SHA: 688177) announced a license and commercialization agreement...

Company Deals

3D Medicines and CATUG Biotech Forge Strategic Alliance in mRNA-LNP Innovation

Fineline Cube Aug 21, 2025

China-based 3D Medicines (HKG: 1244) has entered into a strategic cooperation framework agreement with CATUG Biotechnology....

Company Drug

Bio-Thera Adjusts BAT3306 Clinical Study to Meet Regulatory Standards

Fineline Cube Aug 21, 2025

On August 21, 2025, China-based Bio-Thera Solutions, Ltd. (SHA: 688177) announced a strategic adjustment to...

Company Drug

Novartis’ Atrasentan Approved in China for IgAN Proteinuria Reduction

Fineline Cube Aug 21, 2025

Switzerland-based Novartis (NYSE: NVS) has received approval from China’s National Medical Products Administration (NMPA) for...

Company Drug

Suzhou Zelgen’s ZG005 and Gecacitinib Win NMPA Approval for Advanced Solid Tumors

Fineline Cube Aug 21, 2025

On August 21, 2025, Suzhou Zelgen Biopharmaceuticals Co., Ltd. (SHA: 688266), a China-based company, announced...

Others

Minova’s MI078 Shows Promising Results in Postpartum Depression Trial

Fineline Cube Aug 21, 2025

Nanjing-based Minova Pharmaceuticals Co., Ltd. has announced positive results from a Phase 2 clinical trial...

Company Deals

Abbisko’s ABSK043 Gains IND Approval for KRAS G12C NSCLC in Partnership with Allist

Fineline Cube Aug 21, 2025

Shanghai-based biotech Abbisko Therapeutics Co., Ltd (HKG: 2256) announced that the Center for Drug Evaluation...

Company Drug

Sino Biopharma’s Zongertinib Receives Second Breakthrough Designation for NSCLC

Fineline Cube Aug 21, 2025

On August 20, 2025, Sino Biopharmaceutical Limited (HKG: 1177) announced that its selective HER2 tyrosine...

Company Deals Medical Device

Haohai Biotech Terminates OK Lens Distribution Deal with Brighten Optix Amid Carl Zeiss Acquisition

Fineline Cube Aug 21, 2025

Shanghai Haohai Biological Technology Co., Ltd. (HKG: 6826, SHA: 688366) announced the termination of its...

Company Deals

Nanjing Zenshine Pharma Partners with Cigalah Medpharm to Advance Sebaloxavir Marboxil in MENA

Fineline Cube Aug 21, 2025

On August 21, 2025, Nanjing Zenshine Pharmaceuticals Co., Ltd, a China-based developer of small molecule...

Policy / Regulatory

China Releases Draft Guidelines for Single-Arm Oncology Trials to Support Drug Approvals

Fineline Cube Aug 21, 2025

On August 20, 2025, the Center for Drug Evaluation (CDE) of the National Medical Products...

Company

Ascentage Pharma Reports H1 2025 Financial Results, Shows Strong Growth in Olverembatinib Sales

Fineline Cube Aug 21, 2025

China-based Ascentage Pharma (NASDAQ: AAPG; HKG: 6855) reported its financial results for the first half...

Company Drug

Chongqing Genrix Bio Pharmaceutical’s GR1802 Injection Receives NMPA Approval for Seasonal Allergic Rhinitis in Adolescents

Fineline Cube Aug 20, 2025

China-based Chongqing Genrix Biopharmaceutical Co., Ltd (SHA: 688443) has announced that its investigational product, GR1802...

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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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