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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

Betta Pharmaceuticals’ MCLA-129 Approved for Clinical Trial in Advanced Solid Tumors

Fineline Cube Nov 20, 2024

China’s Betta Pharmaceuticals (SHE: 300558) has announced that it has received clinical trial approval from...

Company Deals

Hangzhou Jiuyuan Gene Engineering Plans HKEX IPO to Raise Up to USD 73.2 Million

Fineline Cube Nov 20, 2024

Hangzhou Jiuyuan Gene Engineering Co., Ltd. is poised to conduct an initial public offering (IPO)...

Company Deals Drug

Shanghai Junshi Biosciences Enters Licensing Agreement for Dual-Targeted Fusion Proteins

Fineline Cube Nov 20, 2024

Shanghai Junshi Biosciences Co., Ltd (HKG: 1877; SHA: 688180), a China-based biopharmaceutical company, has announced...

Company Drug

Biogen and Samsung Bioepis Win EC Approval for Opuviz Biosimilar in Europe

Fineline Cube Nov 20, 2024

US-based Biogen Inc. (NASDAQ: BIIB) and South Korea’s Samsung Bioepis Co., Ltd. have jointly announced...

Company Deals

LaNova Medicines Inks Licensing Deal with Sino Biopharmaceutical for Cancer Therapies in China

Fineline Cube Nov 20, 2024

Shanghai-based LaNova Medicines Ltd, a developer of cancer therapies, has announced another licensing deal, signing...

Company Deals

Worg Pharmaceuticals Secures Major Financing for Allergy and Autoimmune Disease Therapies

Fineline Cube Nov 20, 2024

Worg Pharmaceuticals (Zhejiang) Co., Ltd., a China-based biopharmaceutical company specializing in the development of immunotherapies...

Company

Abbott Laboratories Expands Global Diabetes Care with New Kilkenny Facility

Fineline Cube Nov 19, 2024

Abbott Laboratories (NYSE: ABT), a leading US healthcare company, has announced the opening of its...

Company Medical Device

AbbVie’s Elahere Receives EC Approval for FRα-Positive Ovarian Cancer Treatment

Fineline Cube Nov 19, 2024

US-based AbbVie (NYSE: ABBV) has announced the European Commission (EC) approval for its antibody drug...

Company Drug

Rona Therapeutics’ RN0191 Showcases Positive Phase I Results at AHA Scientific Sessions

Fineline Cube Nov 19, 2024

Shanghai-based nucleic acid drug developer Rona Therapeutics has announced the presentation of positive Phase I...

Company Drug

Eli Lilly’s Tirzepatide Meets Primary Endpoints in Phase III SUMMIT Heart Failure Study

Fineline Cube Nov 19, 2024

Eli Lilly and Company (NYSE: LLY), a leading US pharmaceutical corporation, has announced positive results...

Company Deals

Zai Lab Ltd Announces Secondary Public Offering Worth $230 Million

Fineline Cube Nov 19, 2024

Zai Lab Ltd (ZLAB; NASDAQ: ZLAB; HKG: 9688), a leading biopharmaceutical company, is set to...

Company Drug

AstraZeneca’s Tagrisso Receives Positive CHMP Opinion for EGFR-Mutated NSCLC

Fineline Cube Nov 19, 2024

AstraZeneca (AZ, NASDAQ: AZN), a leading UK pharmaceutical company, has announced that the Committee for...

Company Drug

Everest Medicines’ Nefecon Receives Full Approval from South Korea’s MFDS for IgAN Treatment

Fineline Cube Nov 19, 2024

China-based Everest Medicines (HKG: 1952) has announced that it has received full approval from the...

Company Drug

Eli Lilly’s Muvalaplin Demonstrates Potent Lp(a) Reduction in Phase II Study

Fineline Cube Nov 19, 2024

Eli Lilly & Co. (NYSE: LLY), a leading US pharmaceutical company, has announced positive results...

Company Drug

Sunshine Guojian Pharmaceutical’s SSGJ-608 Files for NMPA Approval in Plaque Psoriasis

Fineline Cube Nov 19, 2024

Sunshine Guojian Pharmaceutical (Shanghai) Co., Ltd, (SHA: 688336) a subsidiary of 3SBio Inc. (HKG: 1530),...

Company Drug

Huahui Health’s Libevitug Earns FDA Breakthrough Designation for Chronic Hepatitis Delta Virus

Fineline Cube Nov 19, 2024

Beijing-based biotech company Huahui Health, specializing in viral hepatitis, hepatology, and oncology, has announced that...

Company Medical Device

Xeltis AG Enrolls First Patient in US Pivotal Trial for aXess with FDA BTD Status

Fineline Cube Nov 19, 2024

Holland-based Xeltis AG has announced the enrollment of the first patient in a US-staged pivotal...

Company Deals

Shanghai Leadingtac Pharmaceutical Secures $13.81 Million in Series A Financing

Fineline Cube Nov 19, 2024

Shanghai Leadingtac Pharmaceutical Co., Ltd., a China-based small molecule drug developer, has announced the successful...

Company Drug

Huadong Medicine’s DR10624 Receives NMPA Approval for MAFLD and MASH Clinical Trials

Fineline Cube Nov 19, 2024

China-based Huadong Medicine Co., Ltd (SHE: 000963) has announced that it has received approval from...

Policy / Regulatory

NMPA’s CDE Issues Guidelines for Leveraging Real-World Data in Drug Regulation

Fineline Cube Nov 19, 2024

The Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA) has released...

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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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