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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

Chia Tai Tianqing Launches NPP for Urgent Cancer Treatment in Hong Kong

Fineline Cube Mar 31, 2025

China-based Chia Tai Tianqing Pharmaceutical has entered into a Named Patient Program (NPP) collaboration with...

Company Drug

Innovent Biologics’ IBI363 Granted Breakthrough Therapy Designation for Melanoma

Fineline Cube Mar 31, 2025

China-based Innovent Biologics, Inc. (HKG: 1801) announced that it has received breakthrough therapy designation (BTD)...

Hospital Policy / Regulatory

NHC Data Reveals Digital Leap for Class 3 Hospitals Amid Drug Cost Crackdown

Fineline Cube Mar 31, 2025

China’s 2,168 Class 3 public hospitals demonstrated enhanced fiscal discipline in 2023, with medical services...

Company Drug

Hengrui’s HRS-5965 Granted Breakthrough Therapy Designation for IgA Nephropathy

Fineline Cube Mar 31, 2025

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

Company Drug

Sanofi’s Dupixent Approved in Japan for Chronic Obstructive Pulmonary Disease

Fineline Cube Mar 31, 2025

Sanofi (EPA: SAN, NASDAQ: SNY) announced that it has received approval from Japan’s Ministry of...

Company Deals

Pacific Shuanglin Bio-pharmacy Partners with XtalPi for Blood Product Innovation

Fineline Cube Mar 31, 2025

China-based Pacific Shuanglin Bio-pharmacy Co., Ltd (SHE: 000403) has formed a strategic partnership with Shenzhen-based...

Company Drug

Novartis’ Pluvicto Gains Expanded FDA Approval for Prostate Cancer Treatment

Fineline Cube Mar 31, 2025

Swiss pharmaceutical giant Novartis (NYSE: NVS) announced that it has received expanded indication approval from...

Company Drug

EMA’s CHMP Issues Negative Opinion on Lilly’s Kisunla for Alzheimer’s

Fineline Cube Mar 31, 2025

The Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA)...

Policy / Regulatory

China’s IAC Drafts Commercial Health Insurance Drug List A-Series to Bridge NRDL Coverage Gaps

Fineline Cube Mar 31, 2025

The Insurance Association of China (IAC) has unveiled its inaugural draft for the Commercial Health...

Policy / Regulatory

China Scraps Outpatient Prepayment in Public Hospitals by 2025: Healthcare Reform Shifts Financial Burden

Fineline Cube Mar 31, 2025

The National Health Commission (NHC) will eliminate outpatient prepayment requirements across public medical institutions by...

Company

uBriGene Appoints Dr. Joy Zhou to Lead Cell Therapy Development

Fineline Cube Mar 31, 2025

China-based advanced therapy medicinal product (ATMP) contract development and manufacturing organization (CDMO) uBriGene Biosciences announced...

Company Drug

BMS’s Opdivo/Yervoy Combo Approved by NMPA for First-Line HCC Treatment

Fineline Cube Mar 31, 2025

Bristol-Myers Squibb (BMS, NYSE: BMY) announced that it has received approval from China’s National Medical...

Company Drug

Roche’s Ocrevus Approved by China’s NMPA for Multiple Sclerosis Treatment

Fineline Cube Mar 31, 2025

Swiss pharmaceutical giant Roche (SWX: ROG, OTCMKTS: RHHBY) announced that it has received marketing approval...

Company Medical Device

Shanghai Bio-heart Launches SAKURA-SCB Study for Drug-Coated Balloon in Japan

Fineline Cube Mar 31, 2025

China-based Shanghai Bio-heart Biological Technology Co., Ltd (HKG: 2185) announced the first patient enrollment for...

Company Drug

AstraZeneca’s Imfinzi Approved by FDA for Bladder Cancer Treatment

Fineline Cube Mar 31, 2025

The US Food and Drug Administration (FDA) has approved AstraZeneca’s (NASDAQ: AZN) PD-L1 inhibitor Imfinzi...

Company

MicroPort Endovascular Reports 1.61% Revenue Growth in 2024 with Strong Profit Increase

Fineline Cube Mar 31, 2025

Shanghai MicroPort Endovascular MedTech Co., Ltd (SHA: 688016) released its 2024 financial report, showing a...

Company

Luye Pharma Group Reports 2024 Revenue Dip Despite Growth in Product Sales

Fineline Cube Mar 31, 2025

China-based Luye Pharma Group (HKG: 2186) announced its 2024 financial performance, recording RMB 6.061 billion...

Company

Hengrui Pharmaceuticals Reports 22.63% Revenue Growth in 2024 with Strong Innovative Drug Sales

Fineline Cube Mar 31, 2025

China-based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276) released its 2024 financial report, recording RMB...

Company Drug Medical Device

Sanofi’s Qfitlia Approved by FDA for Hemophilia A and B Prophylaxis

Fineline Cube Mar 31, 2025

France-based Sanofi (EPA: SAN, NASDAQ: SNY) has announced receiving marketing approval from the US Food...

Company Drug

Brii Biosciences Presents Elebsiran Phase II Data at APASL 2025 Meeting

Fineline Cube Mar 31, 2025

China-based Brii Biosciences Ltd (HKG: 2137) has published the latest data from its ongoing Phase...

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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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