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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

FDA Approves Precigen’s Papzimeos for Recurrent Respiratory Papillomatosis”

Fineline Cube Aug 15, 2025

The U.S. Food and Drug Administration (FDA) has approved Papzimeos (zopapogene imadenovec-drba), developed by Precigen,...

Company Deals

Shanghai Pharmaceuticals and Baxter China Forge Strategic Partnership for Anesthesia Products

Fineline Cube Aug 15, 2025

Shanghai Pharmaceuticals Holding Co., Ltd. (SPH, HKG: 2607, SHA: 601607) announced the signing of a...

Company

CARsgen Therapeutics Reports 2025 Interim Results and Regulatory Progress

Fineline Cube Aug 15, 2025

CARsgen Therapeutics Holdings Limited (HKG: 2171) has announced its 2025 Interim Results, highlighting significant progress...

Company Deals

Superluminal Collaborates With Eli Lilly on Small Molecule Therapeutics for Cardiometabolic Diseases

Fineline Cube Aug 15, 2025

Superluminal Medicines announced on August 14, 2025, a collaboration with Eli Lilly (NYSE: LLY) to...

Company Drug

Sanofi’s Rilzabrutinib Granted Orphan Drug Designation for IgG4-Related Disease by EMA

Fineline Cube Aug 15, 2025

French pharmaceutical major Sanofi (NASDAQ: SNY) announced that it has received another orphan drug designation...

Policy / Regulatory

China’s NHSA Releases Interim Measures for Medical Case-Based Payment Management

Fineline Cube Aug 15, 2025

The National Healthcare Security Administration (NHSA) issued the “Interim Measures for Medical Security Case-Based Payment...

Company Drug

Pfizer’s Emblaveo Prescribed in Shanghai Hospitals for First Time Nationwide

Fineline Cube Aug 15, 2025

US giant Pfizer Inc. (NYSE: PFE) announced that its Emblaveo (aztreonam and avibactam) has been...

Company Drug

Insilico Medicine’s ISM8969 Nears Clinical Evaluation for Parkinson’s Disease

Fineline Cube Aug 15, 2025

Insilico Medicine, a Chinese generative AI-driven biotech company, announced the completion of IND-enabling studies for...

Company Drug

SineuGene’s First-in-Class ALS Gene Therapy SNUG01 Gets NMPA Clinical Trial Clearance

Fineline Cube Aug 15, 2025

Beijing-based SineuGene Therapeutics, a developer of gene therapies for brain disorders based in Beijing, announced that...

Company Deals

Fosun Pharma Issues China’s First Private Pharma Innovation Bond to Accelerate R&D

Fineline Cube Aug 15, 2025

Shanghai-based Fosun Pharmaceutical (Group) Co., Ltd (SHA: 600196, HKG: 2196) has successfully issued the nation’s first...

Company Drug

Eli Lilly Hikes Mounjaro Price in UK by 170% for Private-Pay Patients

Fineline Cube Aug 15, 2025

US pharmaceutical giant Eli Lilly & Co. (NYSE: LLY) announced on August 14, 2025, that...

Company Drug

Qihan Biotech’s QT-019B Gains FDA IND Approval for Autoimmune Diseases

Fineline Cube Aug 15, 2025

Hangzhou Qihan Biotech Co., Ltd. announced that its self-developed universal dual-target CAR-T cell product, QT-019B,...

Company Drug

Novartis’ Ianalumab Shows Positive Results in Phase 3 Trials for ITP and Sjögren’s Disease

Fineline Cube Aug 14, 2025

Swiss pharmaceutical giant Novartis (NYSE: NVS) announced positive top-line results from the Phase 3 VAYHIT2...

Company Drug

Everest Medicines’ Velsipity NDA Accepted for Review in Taiwan

Fineline Cube Aug 14, 2025

China-based Everest Medicines (HKG: 1952) announced that the New Drug Application (NDA) for its Velsipity...

Company Drug

Hualan Biological Gains NMPA Approval for Hib Vaccine Clinical Trials

Fineline Cube Aug 14, 2025

Hualan Biological Engineering Inc., (SHE: 002007) announced that its freeze-dried Haemophilus influenzae type b (Hib)...

Company Drug

RemeGen Announces Positive Phase III Results for Telitacicept in Primary Sjögren’s Syndrome

Fineline Cube Aug 14, 2025

China-based RemeGen Co., Ltd. (SHA: 688331, HKG: 9995), a China-based pharmaceutical firm, announced on August...

Hospital Medical Device Policy / Regulatory

China Issues Guidelines for Medical Advertisement Identification, Clarifies Scenarios and Regulations

Fineline Cube Aug 14, 2025

The State Administration for Market Regulation (SAMR), in collaboration with the National Health Commission (NHC)...

Company Drug

MSD Officially Launches Zerbaxa in China to Tackle Drug-Resistant Infections

Fineline Cube Aug 14, 2025

US-based Merck, Sharp & Dohme Inc. (MSD; NYSE: MRK) announced on August 13, 2025, the...

Company

Jiangsu Hengrui Establishes New Biopharmaceutical Unit to Strengthen Anesthesia and ICU Presence

Fineline Cube Aug 14, 2025

China-based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (HKG: 1276, SHA: 600276) announced on August 14, 2025,...

Company Drug

Jiangsu Hengrui’s Combo Therapy Approved for Clinical Trials by NMPA

Fineline Cube Aug 14, 2025

China-based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (HKG: 1276, SHA: 600276) announced on August 13, 2025,...

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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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