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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

Luye Pharma’s BA1302 Receives FDA Orphan Drug Designation for Lung and Pancreatic Cancer

Fineline Cube Mar 27, 2025

China-based Luye Pharma Group’s (HKG: 2186) controlling subsidiary Shandong Boan Biotechnology Co., Ltd (HKG: 6955)...

Company Deals

Insilico Medicine Collaborates with Mabwell Bio to Enhance ADC R&D with AI

Fineline Cube Mar 27, 2025

China’s generative artificial intelligence (AI)-driven biotech Insilico Medicine has entered into a collaboration with compatriot...

Company Deals

Bayer Inks Licensing Deal for Suzhou Puhe’s PRMT5 Inhibitor, BAY 3713372

Fineline Cube Mar 27, 2025

German pharmaceutical giant Bayer (ETR: BAYN) has entered into a licensing agreement with Suzhou Puhe...

Company Drug

AstraZeneca’s Calquence Approved by NMPA for CLL/SLL Treatment

Fineline Cube Mar 27, 2025

UK pharmaceutical major AstraZeneca (NASDAQ: AZN) has announced receiving another indication approval from China’s National...

Company Medical Device

Shanghai ZJ Bio-Tech’s HCV Nucleic Acid Test Kit Receives NMPA Approval

Fineline Cube Mar 27, 2025

China-based molecular diagnostic reagent specialist Shanghai Liferiver Bio-Tech Co., Ltd (SHA: 688317) has announced receiving...

Company Deals

Shanghai RAAS Plans RMB4.2 Billion Acquisition of Nanyue BioPharming to Boost Plasma Resources

Fineline Cube Mar 27, 2025

China’s Shanghai RAAS (SHE: 002252) has announced plans to acquire 100% stakes in compatriot firm...

Company Drug

Sichuan Huiyu Pharmaceutical Wins Marketing Approvals in Italy, Portugal, Saudi Arabia

Fineline Cube Mar 27, 2025

China-based Sichuan Huiyu Pharmaceutical Co., Ltd (SHA: 688553) has announced its its subsidiaries Seacross Pharma...

Company Deals

Merck KGaA Partners with Roche to Commercialize Tepmetko in China

Fineline Cube Mar 26, 2025

Germany-based pharmaceutical giant Merck KGaA (ETR: MRK) has entered into a partnership with Swiss giant...

Company Hospital

China Resources Medical Holdings Reports 2024 Revenue of RMB9.86 Billion Amid Net Profit Surge

Fineline Cube Mar 26, 2025

China Resources Medical Holdings Company Ltd (CR Medical, HKG: 1515) has published its 2024 financial...

Company Drug

GSK’s Blujepa Approved by FDA for Uncomplicated Urinary Tract Infections

Fineline Cube Mar 26, 2025

UK-based pharmaceutical company GlaxoSmithKline (GSK; NYSE: GSK) announced that it has received marketing approval from...

Company Drug

Guangzhou Doublle Bioproduct Receives IND Approval for E101 in Type 2 Diabetes

Fineline Cube Mar 26, 2025

Guangzhou Doublle Bioproduct Co., Ltd. has announced receiving Investigational New Drug (IND) clearance from China’s...

Company

WuXi Biologics Reports 9.6% Revenue Growth in 2024, Expanding CRDMO Services

Fineline Cube Mar 26, 2025

China-based Contract Research, Development and Manufacturing Organization (CRDMO) WuXi Biologics (HKG: 2269) has released its...

Company Drug

Sanofi’s Tolebrutinib Accepted for FDA Review in Non-Relapsing Secondary Progressive Multiple Sclerosis

Fineline Cube Mar 26, 2025

Sanofi (EPA: SAN, NASDAQ: SNY) announced that a market filing for its tolebrutinib as a...

Company

Fosun Pharma’s 2024 Revenue Reaches RMB 41.1 Billion Amid R&D Investment

Fineline Cube Mar 26, 2025

China-based Shanghai Fosun Pharmaceutical (Group) Co., Ltd (SHA: 600196, HKG: 2196) has released its 2024...

Company

Burning Rock Reports Q4 Revenue Growth Amid Improved Profitability

Fineline Cube Mar 26, 2025

Guangzhou-based medical device company Burning Rock (NASDAQ: BNR) has released its Q4 2024 financial results....

Policy / Regulatory

China’s 2025 Pharmacopoeia Edition Approved, Set for October 1 Implementation

Fineline Cube Mar 26, 2025

The Pharmacopoeia of the People’s Republic of China (2025 Edition), released by the National Medical...

Company

Alphamab Oncology Reports 192.58% Revenue Surge Led by Envafolimab

Fineline Cube Mar 26, 2025

Alphamab Oncology (HKG: 9966) has announced its 2024 financial results, marking a significant milestone with...

Company Drug

Shanghai Henlius Biotech Receives NMPA Approval for HLX79 in Glomerulonephritis Trial

Fineline Cube Mar 26, 2025

China’s Shanghai Henlius Biotech Inc. (HKG: 2696) has announced receiving approval from the National Medical...

Company Drug

Chia Tai Tianqing’s TQB2210 Approved for Advanced Malignant Tumor Study

Fineline Cube Mar 26, 2025

The Center for Drug Evaluation (CDE) of China’s National Medical Products Administration (NMPA) has approved...

Company Deals

CanSino Biologics Partners with Saudi SPIMACO to Boost Meningococcal Vaccine Access

Fineline Cube Mar 26, 2025

China-based CanSino Biologics Inc. (HKG: 6185) has entered into a collaboration agreement with Saudi pharmaceutical...

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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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