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Company Deals

Astellas and Vir Biotechnology Partner on $1.7B+ PRO-XTEN TCE Deal – VIR-5500 Targets PSMA in Prostate Cancer

Fineline Cube Feb 25, 2026
Company Deals

MGI Tech Sells Complete Genomics to Swiss Rockets for $50M – Divests US Unit to Mitigate Geopolitical Risks

Fineline Cube Feb 25, 2026
Company Deals

Junshi Biosciences Partners with Antengene on Cancer Combination – JS207 PD‑1/VEGF Bispecific Plus ATG‑037 CD73 Inhibitor

Fineline Cube Feb 25, 2026
Company Deals

Dartsbio Licenses PACAP Antibody DS009 to Slate Medicines – $130M Series A Fuels Global Migraine Development

Fineline Cube Feb 25, 2026
Company Deals

Henlius Licenses Serplulimab to Abbott for Emerging Markets – Expands Anti‑PD‑1 Global Footprint

Fineline Cube Feb 25, 2026
Policy / Regulatory

FDA Issues Draft Guidance on Plausible Mechanism Framework – Accelerates Approval Pathway for Individualized Genetic Therapies

Fineline Cube Feb 24, 2026
Company Drug

FDA Approves AstraZeneca’s Calquence Plus Venetoclax for CLL/SLL – First All‑Oral Fixed‑Duration Regimen

Fineline Cube Feb 25, 2026
Company Drug

Dupixent Wins FDA Approval for Allergic Fungal Rhinosinusitis – First Targeted Therapy for AFRS Expands Dupilumab Label

Fineline Cube Feb 25, 2026
Company Policy / Regulatory

AstraZeneca Challenges US Government’s Drug Price Negotiation Plan for Medicare

Fineline Cube Aug 28, 2023

UK-based pharmaceutical giant AstraZeneca (AZ, NASDAQ: AZN) has filed a legal claim against the US...

Company Drug

MSD Initiates Phase III Trial for PCSK9 Inhibitor MK-0616 in LDL Cholesterol Reduction

Fineline Cube Aug 28, 2023

Merck, Sharp & Dohme (MSD; NYSE: MRK) has commenced Phase III development for its experimental...

Company Deals

Henlius Biotech Expands Licensing Agreement with KGbio for PD-1 Inhibitor

Fineline Cube Aug 28, 2023

Shanghai Henlius Biotech Co., Ltd (HKG: 2696) has announced an update to the licensing agreement...

Company Drug

Sandoz Receives FDA Clearance for First Biosimilar to Biogen’s Tysabri

Fineline Cube Aug 28, 2023

The Sandoz unit of Switzerland-based Novartis (NYSE: NVS) has received regulatory clearance from the US...

Policy / Regulatory

CDE Seeks Public Feedback on Biological Product Changes During Clinical Trials

Fineline Cube Aug 28, 2023

The Center for Drug Evaluation (CDE) is once again seeking public feedback on two key...

Company Deals

Chinese Pharma Consortium Eyes Poland’s Neuca in Strategic European Market Acquisition

Fineline Cube Aug 28, 2023

A consortium of China-based pharmaceutical companies, potentially including the state-owned giant Sinopharm (HKG: 1099), is...

Company Drug

Tasly Pharmaceuticals Gets NMPA Approval for STRO-002 Clinical Study in Solid Tumors

Fineline Cube Aug 28, 2023

China-based Tasly Pharmaceuticals (SHA: 600535) has announced that it has received approval from the National...

Company Deals

CanSino Biologics to Expand Southeast Asian Presence with Solution Group Berhad Stake

Fineline Cube Aug 28, 2023

China-based CanSino Biologics (SHA: 688185, HKG: 6185) is poised to acquire an undisclosed amount of...

Company Drug

Youcare Pharmaceutical’s YKYYO17 Receives Ethical Approval for COVID-19 Treatment Study

Fineline Cube Aug 28, 2023

China-based Youcare Pharmaceutical Group (SHA: 688658) has received ethical approval from the China-Japan Friendship Hospital...

Company Drug

Novartis Defends Entresto Patents as Generic Approvals Trigger Legal Response

Fineline Cube Aug 28, 2023

On August 24, 2023, generic versions of Novartis’ (NYSE: NVS) heart failure therapy Entresto (sacubitril,...

Company Drug

Jiangsu Hengrui Submits Market Approval Filing for SHR0302 in Ankylosing Spondylitis

Fineline Cube Aug 28, 2023

China-based Jiangsu Hengrui Pharmaceuticals Co., Ltd (SHA: 600276) has announced that a market approval filing...

Company Deals

CSH MEDI Secures Series A+ Funding to Advance Biomagnetic Equipment Technology

Fineline Cube Aug 28, 2023

CSH MEDI, a Shanghai-based biomagnetic equipment manufacturer, has reportedly raised close to RMB 100 million...

Company Drug

Junshi Biosciences’ Senaparib NDA Accepted by NMPA for Ovarian Cancer Maintenance Treatment

Fineline Cube Aug 28, 2023

China’s Junshi Biosciences (HKG: 1877; SHA: 688180) has announced that the New Drug Application (NDA)...

Company

Luye Pharma Group’s Subsidiary Boan Biotechnology Reports 18.4% Revenue Growth in H1 2023

Fineline Cube Aug 28, 2023

China-based Luye Pharma Group’s (HKG: 2186) controlling subsidiary, Shandong Boan Biotechnology Co., Ltd (HKG: 6955),...

Policy / Regulatory

CSRC Aims to Rebalance Primary and Secondary Markets with New Regulatory Measures

Fineline Cube Aug 28, 2023

The China Securities Regulatory Commission (CSRC) has released a document with the aim of “rebalancing”...

Company Deals

Neurodawn Pharmaceutical and China Medical System Holdings Ink Licensing Deal for Y-3

Fineline Cube Aug 25, 2023

Nanjing-based Neurodawn Pharmaceutical Co., Ltd has entered into a significant licensing deal with China Medical...

Company Drug

Jiangsu Kanion Pharmaceutical Gets NMPA Approval for SLE Clinical Trial with KYS202002A

Fineline Cube Aug 25, 2023

Jiangsu Kanion Pharmaceutical Co., Ltd (SHA: 600557), a prominent China-based pharmaceutical company, has announced that...

Company Drug

Everest Medicines’ Nefecon NDA for IgAN Accepted for Review in Macao

Fineline Cube Aug 25, 2023

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

Policy / Regulatory

China Releases Third List of Pediatric Drugs to Guide Development and Filings

Fineline Cube Aug 25, 2023

The National Health Commission (NHC), National Healthcare Security Administration, National Medical Products Administration (NMPA), and...

Policy / Regulatory

NMPA Releases 72nd Batch of Reference Drugs for GQCE

Fineline Cube Aug 25, 2023

The National Medical Products Administration (NMPA) has released the 72nd batch of reference drugs for...

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Recent updates

  • FDA Approves AstraZeneca’s Calquence Plus Venetoclax for CLL/SLL – First All‑Oral Fixed‑Duration Regimen
  • Dupixent Wins FDA Approval for Allergic Fungal Rhinosinusitis – First Targeted Therapy for AFRS Expands Dupilumab Label
  • United Labs’ UBT251 Achieves 19.7% Weight Loss in Phase II – Triple‑Target GLP‑1/GIP/GCG Agonist Shows Blockbuster Potential
  • Astellas and Vir Biotechnology Partner on $1.7B+ PRO-XTEN TCE Deal – VIR-5500 Targets PSMA in Prostate Cancer
  • Bio-Thera’s BAT4406F BLA Accepted by NMPA – Next‑Gen Anti‑CD20 mAb for Rare Disease NMOSD
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

FDA Approves AstraZeneca’s Calquence Plus Venetoclax for CLL/SLL – First All‑Oral Fixed‑Duration Regimen

Company Drug

Dupixent Wins FDA Approval for Allergic Fungal Rhinosinusitis – First Targeted Therapy for AFRS Expands Dupilumab Label

Company Drug

United Labs’ UBT251 Achieves 19.7% Weight Loss in Phase II – Triple‑Target GLP‑1/GIP/GCG Agonist Shows Blockbuster Potential

Company Deals

Astellas and Vir Biotechnology Partner on $1.7B+ PRO-XTEN TCE Deal – VIR-5500 Targets PSMA in Prostate Cancer

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