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Company Deals

Xbiome Strikes NewCo‑Style Technology Collaboration with Biogent Therapeutics for AI‑Driven Bispecific Antibody Development

Fineline Cube Aug 14, 2026
Company Deals

ACROBiosystems and Bailinke Pharmaceutical Form Strategic Partnership to Build AI‑Empowered Affinity Purification Solutions

Fineline Cube Aug 14, 2026
Company Deals

IASO Biotherapeutics Completes Acquisition of MediSix Therapeutics – Adding PEBL‑Based CAR‑T Cell Therapy Platform for T‑Cell Malignancies

Fineline Cube Aug 14, 2026
Company Deals

Hybio Pharmaceutical Grants Wansheng Pharmaceutical Exclusive China License for Semaglutide’s Glycemic Control Indication in Up-to-RMB 182.5 Million Deal

Fineline Cube Aug 13, 2026
Company Deals

Insilico Medicine and THPharma Launch AI Research Collaboration to Build ‘Reverse Translation’ Drug Discovery Strategy Around Phase 3 Candidate THP-001

Fineline Cube Aug 13, 2026
Policy / Regulatory

NMPA Releases Draft Implementation Rules for the National Key R&D Program – Public Comment Open Through 12 Sept 2026

Fineline Cube Aug 14, 2026
Company Drug

Yiling Pharmaceutical Files IND in China for LB220-D08, a First-In-Class Factor B Inhibitor for aHUS

Fineline Cube Aug 17, 2026
Company Drug

Pfizer and Valneva See EMA Validate MAA for PF‑07307405, the First‑Potential Blockbuster Lyme Disease Vaccine

Fineline Cube Aug 17, 2026
Company Drug

HealZen Therapeutics Gains NMPA Approval for HZ-A-018 Clinical Study in Autoimmune Diseases

Fineline Cube Jan 30, 2023

Hangzhou-based HealZen Therapeutics has announced receiving approval from the National Medical Products Administration (NMPA) to...

Company Drug

Betta Pharmaceuticals’ BPI-D0316 Accepted for Review by CDE for First-Line NSCLC

Fineline Cube Jan 30, 2023

China-based Betta Pharmaceuticals Co., Ltd (SHE: 300558) has announced that another market approval filing for...

Company Drug

Jiangsu Alpha Biopharma’s Zorifertinib NDA Accepted for Review by CDE

Fineline Cube Jan 30, 2023

China-based Jiangsu Alpha Biopharma Ltd has announced that the New Drug Application (NDA) for its...

Company Drug

Grand Pharma’s Jext Auto-Injector Approved for Import into Greater Bay Area

Fineline Cube Jan 30, 2023

China-based Grand Pharmaceutical Group Limited (HKG: 0512) has announced receiving official approval from the Guangdong...

Company Drug

Abbisko’s ABSK021 Receives FDA Breakthrough Therapy Designation for TGCT

Fineline Cube Jan 30, 2023

Shanghai-based biotech Abbisko Therapeutics Co., Ltd (HKG: 2256) has announced receiving breakthrough therapy designation (BTD)...

Company Drug

CDE Grants Priority Review Status to Kechow’s HL-085 for Melanoma Treatment

Fineline Cube Jan 30, 2023

The Center for Drug Evaluation (CDE) website indicates that Kechow Pharma’s HL-085 is set to...

Company Drug

NMPA Approves Two China-Developed COVID-19 Small-Molecule Therapies

Fineline Cube Jan 29, 2023

The National Medical Products Administration (NMPA) has issued conditional marketing approvals to two novel, China-discovered...

Policy / Regulatory

China’s NHC Issues Guidelines to Improve Pediatric Medication Management

Fineline Cube Jan 29, 2023

The National Health Commission (NHC) has released a notification aimed at refining management measures for...

Policy / Regulatory

China’s Multi-Bureau Plan Aims to Eradicate Cervical Cancer by 2030

Fineline Cube Jan 29, 2023

The National Health Commission (NHC), Ministry of Education, Ministry of Civil Affairs, and six other...

Company Drug

JS InnoPharm’s US Subsidiary Initiates Phase I Trial for AURKA Inhibitor VIC-1911

Fineline Cube Jan 29, 2023

Shanghai-based JS InnoPharm Ltd has announced the initiation of a Phase I clinical study by...

Company Deals

Akeso Receives First $300M Installment from Summit for Bispecific Antibody Ivonescimab

Fineline Cube Jan 29, 2023

Akeso Inc. (HKG: 9926) has announced receiving the first installment of USD 300 million as...

Policy / Regulatory

NMPA Proposes Emergency Use Management Measures for Medical Devices

Fineline Cube Jan 29, 2023

The National Medical Products Administration (NMPA) has released the “Medical Device Emergency Use Management Measures”...

Company Drug

InnoCare’s Gunagratinib Shows Promising Data in Cholangiocarcinoma at ASCO-GI 2023

Fineline Cube Jan 29, 2023

Beijing InnoCare Pharma Tech Co. (HKG: 9969), a China-based biotech specializing in cancer and autoimmune...

Company Drug

Exegenesis Bio Gains FDA Approval for Gene Therapy EXG102-031 in Wet AMD

Fineline Cube Jan 29, 2023

Hangzhou-based clinical stage gene therapy firm Exegenesis Bio has announced receiving approval from the US...

Company Drug

Simcere’s Cosela Receives First Prescription in China for CDK4/6 Inhibition

Fineline Cube Jan 29, 2023

China-based Simcere Pharmaceutical Group (HKG: 2096) has announced the issuance of the first prescription for...

Policy / Regulatory

China Updates Export Controls on Technologies, Adds Gene Editing to List

Fineline Cube Jan 29, 2023

The Ministry of Finance (MOF) has released an updated notification regarding technologies banned and restricted...

Company Drug

Novartis’ Kisqali Receives NMPA Approval for Premenopausal Breast Cancer

Fineline Cube Jan 28, 2023

Swiss pharmaceutical giant Novartis (NYSE: NVS) has announced receiving marketing approval from the National Medical...

Company Drug

Fosun Pharma’s Comirnaty Bivalent Vaccine Approved in Macau for Booster Shots

Fineline Cube Jan 28, 2023

Shanghai Fosun Pharmaceutical (Group) Co., Ltd (SHA: 600196, HKG: 2196) has announced that its Comirnaty...

Company Drug

HuidaGene Receives FDA IND Approval for Ophthalmology Gene Therapy HG004

Fineline Cube Jan 28, 2023

China-based HuidaGene (Shanghai) Biotechnology Co., Ltd has announced receiving Investigational New Drug (IND) approval from...

Company Deals

Yinghe Brain Science Raises RMB 100 Million in Angel Financing Round

Fineline Cube Jan 28, 2023

Shenzhen Yinghe Brain Science Co., Ltd, a China-based neurotechnology firm, has reportedly raised over RMB...

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Recent updates

  • Yiling Pharmaceutical Files IND in China for LB220-D08, a First-In-Class Factor B Inhibitor for aHUS
  • Pfizer and Valneva See EMA Validate MAA for PF‑07307405, the First‑Potential Blockbuster Lyme Disease Vaccine
  • Sino Medical Sciences Wins Turkish Approval for Ghunter Intracranial Thrombectomy Stent – Broadening Global Footprint in Ischemic Stroke Care
  • Bristol-Myers Squibb Secures FDA Approval for Iberdomide Combination in Multiple Myeloma – First‑Ever Nod Based on MRD‑Negative Response Data
  • Xbiome Strikes NewCo‑Style Technology Collaboration with Biogent Therapeutics for AI‑Driven Bispecific Antibody Development
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 Drug

Yiling Pharmaceutical Files IND in China for LB220-D08, a First-In-Class Factor B Inhibitor for aHUS

Company Drug

Pfizer and Valneva See EMA Validate MAA for PF‑07307405, the First‑Potential Blockbuster Lyme Disease Vaccine

Company Medical Device

Sino Medical Sciences Wins Turkish Approval for Ghunter Intracranial Thrombectomy Stent – Broadening Global Footprint in Ischemic Stroke Care

Company Drug

Bristol-Myers Squibb Secures FDA Approval for Iberdomide Combination in Multiple Myeloma – First‑Ever Nod Based on MRD‑Negative Response Data

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