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Company Deals

Junshi Biosciences Secures Global Exclusive Rights to CAS’s Tetravalent Recombinant Dengue Vaccine in Landmark Licensing Deal

Fineline Cube Jun 12, 2026
Company Deals

Kelun-Biotech Receives USD 89 Million Settlement Payment from Medilink Therapeutics Over ADC Pipeline Out-Licensing Dispute

Fineline Cube Jun 12, 2026
Company Deals

HJ Science Launches HK$1.11 Billion IPO on Hong Kong Exchange to Advance Clinical-Stage Pipeline in Autoimmune, Metabolic, and Oncology Therapies

Fineline Cube Jun 12, 2026
Company Deals

Cascade Pharmaceuticals Secures RMB 318 Million Series D Financing to Advance Bile Acid Metabolism Pipeline

Fineline Cube Jun 12, 2026
Company Deals

QuantumPharm (XtalPi) Secures $400 Million AI-Driven Partnership for Best-in-Class GPCR-Targeting Oral Small-Molecule Drug

Fineline Cube Jun 11, 2026
Policy / Regulatory

China’s CDE Releases 107th Batch of Reference Preparations for Generic Drug Consistency Evaluation with 17 New Drugs Added

Fineline Cube Jun 12, 2026
Company Drug

Shouyao Holdings Secures NMPA Approval for Second-Generation ALK Inhibitor CT-707 as First-Line Treatment for ALK-Positive NSCLC

Fineline Cube Jun 12, 2026
Company Drug

Createrna’s MY008211A Becomes China’s First Home-Grown Oral CFB Inhibitor Approved for Paroxysmal Nocturnal Hemoglobinuria

Fineline Cube Jun 12, 2026
Company Drug

Everest Medicines’ Velsipity NDA Accepted in Macau, Poised for First Asian Approval

Fineline Cube Mar 11, 2024

Everest Medicines (HKG: 1952), based in China, has announced that its New Drug Application (NDA)...

Company Drug

Lepu Biotechnology’s MRG004A ADC Gains Fast Track Designation for Pancreatic Cancer

Fineline Cube Mar 11, 2024

Lepu Biotechnology Co., Ltd. (HKG: 2157), based in China, has announced that its in-house developed...

Company Deals

Sichuan Biokin and Bristol-Myers Squibb Activate $800 Million ADC Licensing Deal

Fineline Cube Mar 11, 2024

Sichuan Biokin Pharmaceutical Co., Ltd. (SHA: 688506) has officially activated its licensing and cooperation agreement...

Company Deals

Simnova Secures RMB 200 Million in Series A+ Funding to Advance CAR Therapy Pipeline

Fineline Cube Mar 11, 2024

Simnova, a Shenzhen-based developer of chimeric antigen receptor (CAR) adoptive cell therapies, has successfully raised...

Company Drug

ClouDr Launches Dapagliflozin, Generic Version of AstraZeneca’s Forxiga, After NMPA Approval

Fineline Cube Mar 11, 2024

Hangzhou Kang Ming Information Technology Co., Ltd. (HKG: 9955), known as “ClouDr,” has officially launched...

Company Drug Legal / IP

BeiGene Launches Legal Action Against Sandoz and MSN Over Brukinsa Patent Infringement

Fineline Cube Mar 11, 2024

BeiGene Ltd. (NASDAQ: BGNE; HKG: 6160; SHA: 688235), the China-based biotech firm, has initiated patent...

Company Drug

Eli Lilly Delays Donanemab Action Date as FDA Calls for Advisory Committee Review

Fineline Cube Mar 11, 2024

Eli Lilly (NYSE: LLY) has announced a delay in the action date for its Alzheimer’s...

Policy / Regulatory

China Cracks Down on Medical Insurance Fraud with New Guidelines and Increased Prosecutions

Fineline Cube Mar 11, 2024

China’s Supreme People’s Court, along with the Supreme People’s Procuratorate and the Ministry of Public...

Company Drug

FDA Approves Wegovy for Cardiovascular Risk Reduction in Obese Patients, First of Its Kind

Fineline Cube Mar 11, 2024

The U.S. Food and Drug Administration (FDA) granted an indication extension approval last week to...

Company Drug

Amgen Reports Positive Results for Otezla in Pediatric Psoriasis Trial

Fineline Cube Mar 11, 2024

Amgen (NASDAQ: AMGN) provided an update last week on a late-stage trial evaluating its PDE4...

Company

Merck’s 2023 Annual Report: A Mixed Bag Amid Global Challenges

Fineline Cube Mar 8, 2024

Merck KGaA (ETR: MRK), a leading German chemical, reported a 5.6% decline in its global...

Company

GSK Reports US Adult Non-Flu Vaccination Rates Recover Post-Pandemic

Fineline Cube Mar 8, 2024

GlaxoSmithKline (GSK; NYSE: GSK), a leading pharmaceutical company based in the UK, has reported that...

Company Drug

BMS’s Opdivo Secures FDA Approval for First-Line Urothelial Carcinoma Treatment

Fineline Cube Mar 8, 2024

The US Food and Drug Administration (FDA) has granted Bristol Myers Squibb (BMS; NYSE: BMY)...

Company Drug

BeiGene’s Brukinsa Receives FDA Approval for Relapsed or Refractory Follicular Lymphoma

Fineline Cube Mar 8, 2024

BeiGene Ltd (NASDAQ: BGNE; HKG: 6160; SHA: 688235), a leading biotech company based in China,...

Company Drug

Visen Pharmaceuticals’ TransCon hGH Accepted for Review by China’s NMPA

Fineline Cube Mar 8, 2024

Visen Pharmaceuticals, a joint venture between Denmark-based Ascendis Pharma and Chinese healthcare-focused investment firm Vivo...

Company Deals

Shandong Luoxin Pharmaceutical Partners with Xbiome to Access Microbiome Transplantation Technology

Fineline Cube Mar 8, 2024

Shandong Luoxin Pharmaceutical Group Stock Co., Ltd (SHE: 002793), a pharmaceutical company based in China,...

Company Drug

Shanghai Fosun Pharma Gets NMPA Green Light for Universal NK Cell Therapy GCK-01 Clinical Study

Fineline Cube Mar 8, 2024

Shanghai Fosun Pharmaceutical (Group) Co., Ltd (SHA: 600196, HKG: 2196), a leading pharmaceutical company based...

Company Drug

Novo Nordisk’s Anti-Obesity Drug Wegovy Eyed for China Launch in 2024

Fineline Cube Mar 8, 2024

Novo Nordisk (NYSE: NVO), a leading diabetes company based in Denmark, has reportedly informed investors...

Company Drug

China Grand Pharmaceutical Receives FDA Approval for Post-Surgical Ophthalmic Drug GPN00833

Fineline Cube Mar 8, 2024

China Grand Pharmaceutical and Healthcare Holdings Ltd (HKG: 0512; CGP) has announced that it has...

Company Drug

Shanghai Fosun Pharma Gets NMPA Green Light for XS-02 Solid Tumor Clinical Study

Fineline Cube Mar 8, 2024

Shanghai Fosun Pharmaceutical (Group) Co., Ltd (SHA: 600196, HKG: 2196), a leading pharmaceutical company based...

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Recent updates

  • Junshi Biosciences Secures Global Exclusive Rights to CAS’s Tetravalent Recombinant Dengue Vaccine in Landmark Licensing Deal
  • Shouyao Holdings Secures NMPA Approval for Second-Generation ALK Inhibitor CT-707 as First-Line Treatment for ALK-Positive NSCLC
  • Createrna’s MY008211A Becomes China’s First Home-Grown Oral CFB Inhibitor Approved for Paroxysmal Nocturnal Hemoglobinuria
  • China’s CDE Releases 107th Batch of Reference Preparations for Generic Drug Consistency Evaluation with 17 New Drugs Added
  • Takeda’s Zasocitinib Demonstrates Superior Efficacy Over Deucravacitinib in Phase III Psoriasis Trial with 35% PASI 100 Response Rate
Special Report 2025 Q1: U.S. Targets Chinese Pharma with 200% Tariffs—Will the Global Drug Market Collapse?

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You Missed

Company Deals

Junshi Biosciences Secures Global Exclusive Rights to CAS’s Tetravalent Recombinant Dengue Vaccine in Landmark Licensing Deal

Company Drug

Shouyao Holdings Secures NMPA Approval for Second-Generation ALK Inhibitor CT-707 as First-Line Treatment for ALK-Positive NSCLC

Company Drug

Createrna’s MY008211A Becomes China’s First Home-Grown Oral CFB Inhibitor Approved for Paroxysmal Nocturnal Hemoglobinuria

Policy / Regulatory

China’s CDE Releases 107th Batch of Reference Preparations for Generic Drug Consistency Evaluation with 17 New Drugs Added

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