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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

HealZen and Johnson & Johnson Partner on BTK Degradation Therapeutics

Fineline Cube Jan 13, 2025

China-based Hangzhou HealZen Therapeutics Co., Ltd., in collaboration with the Shanghai Institute of Materia Medica,...

Company Drug

Hengrui Pharmaceuticals Gets NMPA Approval for SHR-1819 Phase II Study

Fineline Cube Jan 13, 2025

China-based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276) has announced that it has received the...

Company Drug

Hengrui Pharmaceuticals Receives NMPA Approval for SHR-4375 Clinical Trial

Fineline Cube Jan 13, 2025

China-based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276) has announced that it has received clinical...

Company Deals

Ouro Medicines Launches with $120M Series A Financing for CM336 Development

Fineline Cube Jan 13, 2025

Ouro Medicines, the licensee of China-based Keymed Biosciences Inc.’s (HKG: 2162) CM336, has successfully launched...

Company Deals

Menarini Group Expands Oncology Pipeline with Insilico Medicine License

Fineline Cube Jan 13, 2025

Italy’s Menarini Group, through its subsidiary Stemline Therapeutics Inc., has entered into a licensing deal...

Company Deals

Zai Lab Secures Rights to Vertex’s Povetacicept in Key Asian Markets

Fineline Cube Jan 13, 2025

China-based biotech Zai Lab Ltd (NASDAQ: ZLAB; HKG: 9688) has announced an exclusive collaboration and...

Company Deals

Eli Lilly in Advanced Talks to Acquire Scorpion Therapeutics for $2.5 Billion

Fineline Cube Jan 13, 2025

US-based Eli Lilly and Company (NYSE: LLY) is reportedly in advanced talks with compatriot firm...

Company Deals

Light Horse Therapeutics Partners with Novartis in First-in-Class Drug Development

Fineline Cube Jan 13, 2025

US-based Light Horse Therapeutics Inc., a small molecule drug developer that recently emerged from the...

Company Deals

Samsung Bioepis and Teva Partner on Biosimilar EPYLLI for US Market

Fineline Cube Jan 13, 2025

South Korea’s Samsung Bioepis and Israel-based Teva Pharmaceutical (NYSE: TEVA) have entered into a license,...

Company Deals

Sepax Technologies Debuts on STAR Market with Soaring IPO Prices

Fineline Cube Jan 13, 2025

Sino-US firm Sepax Technologies Co., Inc. has successfully completed its initial public offering (IPO) on...

Company Drug

Bayer Files for Finerenone Approval in US and China for Heart Failure-Fineline Info & Tech

Fineline Cube Jan 13, 2025

Bayer AG (ETR: BAYN) has announced market filings with the US Food and Drug Administration...

Company Drug

Pfizer’s Sasanlimab Shows Positive Results in Phase III CREST Study

Fineline Cube Jan 13, 2025

US-based Pfizer Inc. (NYSE: PFE) has reported positive topline results from its pivotal Phase III...

Company Drug

NMPA Approves J&J’s FGFR Kinase Inhibitor Balversa for Urothelial Carcinoma

Fineline Cube Jan 13, 2025

China’s National Medical Products Administration (NMPA) has approved Johnson & Johnson’s (J&J; NYSE: JNJ) FGFR...

Company Drug

Doma Biopharma Receives FDA Clearance for DM002 Phase I Study-Fineline Info & Tech

Fineline Cube Jan 13, 2025

China-based Doma Biopharmaceutical (Suzhou) Co., Ltd has announced that it has received clearance from the...

Company Drug

GSK’s Shingrix Prefilled Syringe Accepted for FDA Review

Fineline Cube Jan 13, 2025

UK-headquartered GlaxoSmithKline (GSK; NYSE: GSK) has announced that a market filing for a prefilled syringe...

Policy / Regulatory

NHSA Launches Nationwide Self-Inspection Campaign on Medical Insurance Fund Usage

Fineline Cube Jan 13, 2025

China’s National Healthcare Security Administration (NHSA) released a notification last weekend, mandating designated medical institutions...

Policy / Regulatory

China’s NHSA Implements New Regulations for Medical Insurance Payment Qualifications

Fineline Cube Jan 13, 2025

China’s National Healthcare Security Administration (NHSA) has released the “Regulations on the Management of Medical...

Company

Shenzhen Oculgen Secures Over RMB 100 Million in Series A Funding

Fineline Cube Jan 11, 2025

Shenzhen Oculgen Biomedical Technology Co., Ltd. has successfully completed a Series A financing round, raising...

Company Drug

Fosun Pharmaceutical’s FCN-437c Accepted for NMPA Review for Breast Cancer Treatment

Fineline Cube Jan 11, 2025

Fosun Pharmaceutical (Group) Co., Ltd (HKG: 2196, SHA: 600196) has announced that another market approval...

Company Drug

Hengrui’s SHR4640 Accepted for NMPA Review for Gout and Hyperuricemia Treatment

Fineline Cube Jan 11, 2025

China-based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276) has announced that a market filing for...

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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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