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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

VectorBuilder Partners with Minaris Regenerative Medicine to Enhance Gene Therapy Solutions

Fineline Cube Mar 13, 2024

VectorBuilder, a specialist in genetic engineering based in China, has entered into a strategic partnership...

Company Drug

Bio-Thera Solutions Gets Green Light for Phase Ib/II Study of ADC BAT8008 in Advanced Solid Tumors

Fineline Cube Mar 13, 2024

Guangzhou-based Bio-Thera Solutions (SHA: 688177) has announced that it has received approval from the National...

Company Drug

Betta Pharmaceuticals’ Ensartinib Accepted for FDA Review for First-Line ALK+ NSCLC Treatment

Fineline Cube Mar 13, 2024

Betta Pharmaceuticals (SHE: 300558), a pharmaceutical company based in China, has announced that the market...

Company Drug

CORXEL Gets CDE Green Light for Phase III Aficamten Study in nHCM

Fineline Cube Mar 13, 2024

CORXEL, formerly known as Ji Xing Pharmaceuticals, a China-based pharmaceutical company, has announced that it...

Company Drug

InnoCare Pharma Receives IND Approval in China for BCL2 Inhibitor Combo Therapy

Fineline Cube Mar 13, 2024

InnoCare Pharma (HKG: 9969; SHA: 688428), a Beijing-based biotech company, has announced that it has...

Company Drug

Simcere Pharmaceutical Gets NMPA Approval for Clinical Study of Trispecific Antibody SIM0500

Fineline Cube Mar 13, 2024

Simcere Pharmaceutical Group (HKG: 2096), a biopharmaceutical company based in China, has announced that it...

Company Drug

Fosun Pharmaceutical Gets NMPA Green Light for Phase I Study of Fibrosis Drug HLX6018

Fineline Cube Mar 13, 2024

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

Policy / Regulatory

NMPA Releases 78th Batch of Reference Drugs for Generic Quality Consistency Evaluation

Fineline Cube Mar 13, 2024

The National Medical Products Administration (NMPA) has released the 78th batch of reference drugs for...

Policy / Regulatory

China’s NHC Outlines Cross-departmental Law Enforcement to Strengthen Medical Supervision

Fineline Cube Mar 13, 2024

The National Health Commission (NHC) has issued a set of “Opinions on Strengthening Cross-departmental Law...

Company Deals

Kexing Pharmaceutical Secures Rights for Chia Tai Tianqing’s Generic Ibrance in 11 Countries

Fineline Cube Mar 12, 2024

Kexing Pharmaceutical (SHA: 688136), based in China, has entered into an international collaboration agreement with...

Company Drug

Kelun-Biotech’s A400 Receives Fast-Track Status from FDA for RET Fusion-Positive NSCLC

Fineline Cube Mar 12, 2024

Sichuan Kelun Pharmaceutical Co., Ltd (SHE: 002422) announced that its innovative drug development subsidiary, Sichuan...

Company Drug

Sinocelltech Gains NMPA Approval for Clinical Study of SCTB35 in B-Cell Non-Hodgkin’s Lymphoma

Fineline Cube Mar 12, 2024

Sinocelltech Group Ltd (SHA: 688520), based in China, has announced that it has received clearance...

Company Drug

Huadong Medicine Secures NMPA Approval for HDM1005, Targeting Type 2 Diabetes and Obesity

Fineline Cube Mar 12, 2024

Huadong Medicine Co., Ltd (SHE: 000963), based in China, has announced that it has received...

Company Drug

Innovent and HutchMed’s Combination Therapy Set for Priority Review in China for Advanced Endometrial Cancer

Fineline Cube Mar 12, 2024

China’s Center for Drug Evaluation (CDE) has indicated that the combination therapy of Innovent Biologics...

Company Drug

Sanofi’s Amlitelimab Shows Promising Phase IIb Results in Atopic Dermatitis, Potential for 12-Week Dosing

Fineline Cube Mar 12, 2024

Sanofi (NASDAQ: SNY) announced this week promising results from a Phase IIb study of its...

Company Deals

Jiangsu QYuns Therapeutics Eyes HK IPO to Raise Up to HKD 243 Million for Autoimmune Pipeline

Fineline Cube Mar 12, 2024

Jiangsu QYuns Therapeutics Co., Ltd. (HKG: 2509), based in China, is poised to launch an...

Company

Legend Biotech Reports Q4 and Full-Year 2023 Financials with Focus on Carvykti Milestones

Fineline Cube Mar 12, 2024

Legend Biotech Corporation (NASDAQ: LEGN) has released its financial results for the fourth quarter and...

Company Deals

Gilead Nears Completion of CymaBay Acquisition After Waiting Period Expires

Fineline Cube Mar 12, 2024

Gilead Sciences (NASDAQ: GILD) has moved one step closer to finalizing its cash tender offer...

Company Drug

J&J’s Tremfya Files for Ulcerative Colitis Indication with FDA, Building on Positive Late-Stage Data

Fineline Cube Mar 12, 2024

The US Food and Drug Administration (FDA) has accepted an indication extension filing from Johnson...

Company Drug

Simcere Secures FDA Approval for Clinical Study of Trispecific Antibody SIM0500 in Multiple Myeloma

Fineline Cube Mar 11, 2024

Simcere Pharmaceutical Group (HKG: 2096), based in China, has received approval from the U.S. Food...

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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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