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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

Hengrui Pharmaceuticals Gets NMPA Green Light for KRAS G12C Inhibitor Clinical Trial in Advanced Solid Tumors

Fineline Cube Mar 5, 2024

Jiangsu Hengrui Pharmaceuticals Co., Ltd (SHA: 600276) has received approval from the National Medical Products...

Company Drug

HitGen Secures CDE Approval for Lipisense IND Filing, Advancing Development for Dyslipidemia Treatment

Fineline Cube Mar 5, 2024

HitGen Inc., (SHA: 688222) a China-based pharmaceutical company, has announced that the Investigational New Drug...

Company Drug

ViiV Healthcare Presents Phase I Data for Ultra-Long-Acting Cabotegravir in HIV Treatment and Prevention

Fineline Cube Mar 5, 2024

GlaxoSmithKline (GSK; NYSE: GSK) unit ViiV Healthcare has presented Phase I results for an ultra-long-acting...

Company Deals

Merck Teams Up with C4 Therapeutics for Targeted Protein Degraders in Oncology

Fineline Cube Mar 5, 2024

Merck (NYSE: MRK), a Germany-headquartered science and technology company, has entered into a partnership with...

Company Digital

Innovent Biologics’ Taletrectinib Receives Second NDA Acceptance in China for ROS1 Positive NSCLC

Fineline Cube Mar 5, 2024

Innovent Biologics Inc., (HKG: 1801), a biopharmaceutical company based in China, has announced that the...

Company Drug

BMS Reports Positive Long-Term Data for Zeposia in Multiple Sclerosis Trials

Fineline Cube Mar 4, 2024

Bristol Myers Squibb (BMS; NYSE: BMY) has unveiled results from several Phase III trials for...

Company Drug

BeiGene’s Brukinsa Outperforms Acalabrutinib in MAIC for Relapsed/Refractory CLL, Says BeiGene

Fineline Cube Mar 4, 2024

BeiGene Ltd (NASDAQ: BGNE; HKG: 6160; SHA: 688235) has announced the results of a matching-adjusted...

Company Drug

Merck’s Mavenclad Demonstrates Lasting Efficacy in RMS Patients, New Data Show

Fineline Cube Mar 4, 2024

Merck KGaA (ETR: MRK), a German multinational pharmaceutical, chemical, and life sciences company, has this...

Legal / IP

AlzeCure Pharma’s Alzheimer’s Drug Candidate ACD856 Receives Global Patent Awards

Fineline Cube Mar 4, 2024

AlzeCure Pharma, a Swedish pharmaceutical company, has announced the receipt of patent approval awards for...

Company Deals

Sino-Biocan Secures Series B Funding to Boost Cell and Gene Therapy Production Platforms

Fineline Cube Mar 4, 2024

Sino-Biocan (Shanghai) Biotech Ltd, a provider of automated, modularized, closed cell production platforms for the...

Company Drug

AIM Vaccine Advances Pneumococcal Vaccine and Initiates Phase II Meningococcal Study

Fineline Cube Mar 4, 2024

AIM Vaccine Co., Ltd (HKG: 6660) has delivered a series of updates on the development...

Company Deals

ArkBio Partners with SDODT to Boost ADHD Treatment Marketing and Commercialization

Fineline Cube Mar 4, 2024

Shanghai Ark Biopharmaceutical Co., Ltd (ArkBio), a Chinese biopharmaceutical company, has entered into a partnership...

Company Drug

Hainan Poly Pharm Secures Tentative FDA Approval for Generic Version of UCB’s Briviact

Fineline Cube Mar 4, 2024

Hainan Poly Pharm Co., Ltd (SHE: 300630), a Chinese pharmaceutical company, has announced that it...

Company Drug

BMS’s Yervoy-Opdivo Combo on Track for Breakthrough Therapy Designation in China for CRC

Fineline Cube Mar 4, 2024

The China Center for Drug Evaluation (CDE) website has indicated that the market approval filing...

Company Deals

Beijing Tinavi Medical Technologies to Form Radiotherapy Equipment JV with IM INNO and Celestial Oncology

Fineline Cube Mar 4, 2024

Beijing Tinavi Medical Technologies Co., Ltd (SHA: 688277) has announced its intention to establish a...

Company Drug

Pfizer’s RSV Vaccine Demonstrates Durable Efficacy with Abrysvo Phase III Results

Fineline Cube Mar 4, 2024

Pfizer Inc. (NYSE: PFE) last week reported the outcomes of a Phase III trial for...

Policy / Regulatory

Biden’s Executive Order May Restrict Data Access for China-Based Life Science Firms in the US

Fineline Cube Mar 4, 2024

US President Joe Biden last week issued an Executive Order titled “Preventing Access to Americans’...

Company Drug

Shanghai Fosun Pharma’s GCK-01 CAR-NK Cell Therapy Gets Tacit Clinical Approval from China’s CDE

Fineline Cube Mar 4, 2024

The China Center for Drug Evaluation (CDE) website has indicated that Shanghai Fosun Pharmaceutical (Group)...

Company Drug

J&J’s Rybrevant Secures Full FDA Approval for NSCLC with EGFR Exon 20 Insertions

Fineline Cube Mar 4, 2024

The US Food and Drug Administration (FDA) has granted Johnson & Johnson (J&J; NYSE: JNJ)...

Company Drug

Astellas Launches Late-Stage Trial in Japan for Nonhormonal Menopause Treatment

Fineline Cube Mar 4, 2024

Astellas Pharma Inc. (TYO: 4503), a leading Japanese pharmaceutical company, last week initiated a late-stage...

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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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