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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 Deals

NeuShen Therapeutics Partners with UMass Chan for ALS Gene Therapy Development

Fineline Cube Feb 2, 2023

Sino-US biotech firm NeuShen Therapeutics Inc., focused on central nervous system (CNS) disorders, has announced...

Company Deals

F-Star Therapeutics and Sino Biopharmaceutical Seek CFIUS Approval with Extended Deadline

Fineline Cube Feb 2, 2023

The acquisition of UK-based biologics firm F-Star Therapeutics (NASDAQ: FSTX) by China’s Sino Biopharmaceutical (HKG:...

Company Drug

Jiangsu Hengrui’s SHR8058 Accepted for Review by China’s NMPA for Dry Eye Disease

Fineline Cube Feb 2, 2023

China-based Jiangsu Hengrui Pharmaceuticals (SHA: 600276) has announced that its market filing for the drug...

Company Drug

Nanjing-Based Frontier Biotechnologies Secures Full Approval for Albuvirtide in China

Fineline Cube Feb 2, 2023

Nanjing-based Frontier Biotechnologies Inc. has announced that its supplementary approval filing for albuvirtide, China’s first...

Company Drug

Junshi Biosciences’ JS401 Accepted for Review by China’s NMPA for Hyperlipidemia

Fineline Cube Feb 1, 2023

China-based Junshi Biosciences (HKG: 1877, SHA: 688180) has announced that the National Medical Products Administration...

Company

Pfizer Reports Record Revenues as COVID-19 Sales Soar; 2023 Guidance Amid Market Shifts

Fineline Cube Feb 1, 2023

US-based Pfizer Inc. (NYSE: PFE) reported its Q4 2022 financial results, highlighting an all-time high...

Company Deals Drug

Junshi Biosciences Partners with Huahai for Production of COVID-19 Drug VV116

Fineline Cube Feb 1, 2023

China-based Junshi Biosciences (HKG: 1877, SHA: 688180) has announced a production and supply agreement between...

Company Drug

Ocumension Completes Enrollment for Global Phase III Study of Myopia Treatment OT-101

Fineline Cube Feb 1, 2023

Chinese ophthalmology specialist Ocumension Therapeutics (HKG: 1477) has announced the completion of enrollment for a...

Company Deals

R&B Bio Raises RMB 200 Million in Series A+ Round to Advance Gene Therapy Pipeline

Fineline Cube Feb 1, 2023

Chengdu-based gene therapy firm R&B Biotech has reportedly secured over RMB 200 million (USD 29.64...

Company Drug

Hengrui’s HER2-Targeted ADC SHR-A1811 Gains NMPA Clearance for Clinical Trial

Fineline Cube Feb 1, 2023

China’s Jiangsu Hengrui Pharmaceuticals (SHA: 600276) has announced receiving clearance from the National Medical Products...

Company Drug

Hengrui’s Lutetium [177Lu] Oxy-Octreotide Gains Clinical Clearance in China

Fineline Cube Feb 1, 2023

China’s Jiangsu Hengrui Pharmaceuticals (SHA: 600276) has announced receiving clinical clearance from the National Medical...

Company Drug

Changchun BCHT Gains NMPA Approval for Herpes Zoster Vaccine

Fineline Cube Feb 1, 2023

China-based Changchun BCHT Biotechnology Co., Ltd (SHA: 688276) has announced receiving marketing approval from the...

Company Drug

Jemincare’s Avatrombopag Market Filing Accepted for Review by China’s CDE

Fineline Cube Feb 1, 2023

China-based Jiangxi Jemincare Group has announced that its market filing for avatrombopag maleate (20mg) has...

Company Drug

Ascletis Receives FDA Approval for Phase IIa Trial of ASC10 in RSV Infection

Fineline Cube Feb 1, 2023

China-based Ascletis Pharma Inc. (HKG: 1672) has announced receiving approval from the US FDA to...

Company Deals

Daewoong Pharmaceutical Licenses Bersiporocin to CSP for Greater China Development

Fineline Cube Feb 1, 2023

South Korea-based Daewoong Pharmaceutical has entered into an exclusive licensing agreement with UK-based CS Pharmaceuticals...

Company Drug

Sirnaomics Accelerates STP705 Development After Positive Skin Cancer Trial Results

Fineline Cube Feb 1, 2023

Sirnaomics Ltd (HKG: 2257) is advancing the clinical development of STP705 following positive results from...

Company Drug

Betta Pharmaceuticals Gains FDA Approval for Clinical Trial of BPI-460372

Fineline Cube Feb 1, 2023

China’s Betta Pharmaceuticals (SHE: 300558) has announced receiving clinical trial approval from the US FDA...

Company

Novartis Q4 Results Show Growth in Innovative Medicines Amid Sandoz Spin-Off Plans

Fineline Cube Feb 1, 2023

Swiss pharmaceutical giant Novartis (NYSE: NVS) has released its financial results for Q4 and the...

Company Deals

Zhifei Renews Vaccine Supply Agreement with Merck Sharp & Dohme

Fineline Cube Jan 31, 2023

China-based Chongqing Zhifei Biological Co., Ltd (SHE: 300122) has announced the renewal of a supply,...

Company

Abbott’s Q4 Sales Dip Amid COVID-19 Testing Decline, China Market Updates

Fineline Cube Jan 31, 2023

US-based Abbott (NYSE: ABT) released its Q4 2022 financial results last week, showing a 6.1%...

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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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