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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

Innovent Biologics and ASK Pharma Forge Strategic Partnership for Limertinib in Lung Cancer Treatment

Fineline Cube Oct 8, 2024

China-based Innovent Biologics Inc. (HKG: 1801) and Jiangsu Aosaikang Pharmaceutical Co., Ltd (ASK Pharma, SHE:...

Company Deals

MediLink Therapeutics Partners with Amgen for Clinical Trial in Small Cell Lung Cancer

Fineline Cube Oct 8, 2024

Suzhou-based biotech MediLink Therapeutics (Suzhou) Co., Ltd has announced a partnership with US pharmaceutical giant...

Company

Cassava Sciences to Pay Over USD 40 Million to Settle SEC Charges Over Alzheimer’s Drug Claims

Fineline Cube Oct 8, 2024

The US Securities and Exchange Commission (SEC) has announced that US-based biotech firm Cassava Sciences...

Company Deals

Wuhan YZY Biopharma Grants Rights to CD3/EpCAM Antibody M701 to Chi Ta TianQing Pharma in China

Fineline Cube Oct 8, 2024

Wuhan YZY Biopharma Co., Ltd (HKG: 2496) has announced that it has granted Chi Ta...

Company Deals

Regor Therapeutics Strikes Deal with Genentech for CDK Inhibitors, Fetching USD 850 Million Upfront

Fineline Cube Oct 8, 2024

Regor Therapeutics Group, a US-based biotech with significant ties to China, has entered into a...

Company Drug

China’s CDE Announces “Care Plan” to Include Pfizer’s Marstaximab for Rare Disease Drug Development

Fineline Cube Oct 8, 2024

The National Health Commission (NHC) of China, through its Center for Drug Evaluation (CDE), has...

Company Deals

Genor Biopharma to Acquire EOC Pharma Group in a Merger Deal, Eyeing Commercialization Synergies

Fineline Cube Oct 8, 2024

Genor Biopharma Holdings Limited (HKG: 6998) has announced a definitive merger agreement with EOC Pharma...

Company

WuXi AppTec and WuXi Biologics Weigh Asset Sales in US and Europe Over Biosecure Act Concerns

Fineline Cube Oct 8, 2024

Reports emerged last week in the Financial Times suggesting that WuXi AppTec (HKG: 2359) and...

Company Deals

Tigermed Announces Acquisition of Majority Stake in Shanghai Guanhe Pharmaceutical for CNY 140 Million

Fineline Cube Oct 8, 2024

Tigermed (SHE: 300347, HKG: 3347) has announced its intention to acquire a 40.5650% stake in...

Policy / Regulatory

China’s National Healthcare Security Administration Issues Draft Guidelines for Long-Term Care Insurance

Fineline Cube Oct 8, 2024

The National Healthcare Security Administration (NHSA) has released the “Draft Technical Guidelines for the Preparation...

Company Deals

Insilico Medicine and Seto Biopartner to Leverage AI in Synthetic Biology and Drug Discovery

Fineline Cube Oct 8, 2024

Insilico Medicine has announced a strategic partnership with Seto Bio (SHE: 300583) to harness cutting-edge...

Policy / Regulatory

China’s CDE Releases Draft Guidelines for Biosimilar Drug Labeling

Fineline Cube Oct 8, 2024

On September 29, 2024, the Center for Drug Evaluation (CDE) of China’s National Medical Products...

Company R&D

Legend Biotech Corporation to Establish Advanced R&D Center in Philadelphia for Next-Generation Cell Therapies

Fineline Cube Oct 8, 2024

Legend Biotech Corporation (NASDAQ: LEGN), a leading chimeric antigen receptor (CAR) T cell therapy specialist...

Company Drug

BeiGene Prices TEVIMBRA 10% Below Competitors Following FDA Approval for Esophageal Cancer Treatment

Fineline Cube Oct 7, 2024

BeiGene (NASDAQ: BGNE; HKG: 6160; SHA: 688235) has announced the commercial availability of TEVIMBRA (Tislelizumab)...

Company Drug

Unixell Advances in Cell Therapy with CDE IND Acceptance

Fineline Cube Oct 6, 2024

Shanghai-based Unixell Biotechnology Co., Ltd. has announced that its Investigational New Drug (IND) application for...

Company Drug

Duality Biotherapeutics’ BDCA2 ADC DB-2304 Phase I Trial Registered on ClinicalTrials.gov

Fineline Cube Oct 5, 2024

Duality Biologics, Inc., a biopharmaceutical company specializing in the development of innovative therapies, has registered...

Company Drug

BeiGene’s FGFR2b ADC BG-C137 Enters Phase I Clinical Trial for Advanced Solid Tumors

Fineline Cube Oct 5, 2024

On October 3, 2024, BeiGene (NASDAQ: BGNE; HKG: 6160; SHA: 688235) registered a Phase I...

Company Drug

BMS Expands Opdivo Indication with FDA Approval for NSCLC Combo Therapy

Fineline Cube Oct 4, 2024

The U.S. Food and Drug Administration (FDA) has granted approval for Bristol Myers Squibb’s (BMS,...

Company Drug

InnoCare Pharma’s Orelabrutinib Achieves Milestone in SLE Clinical Trial Enrollment

Fineline Cube Oct 4, 2024

InnoCare Pharma announced on October 4, 2024, that it has completed patient enrollment in a...

Company Drug

Akeso Biopharma’s PD-1/VEGF Bispecific Antibody Study Completes Enrollment

Fineline Cube Oct 4, 2024

On October 4, 2024, Summit Therapeutics (referred to as “Summit”), a partner of Akeso Biopharma...

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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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