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Company Deals

Saizeng Medical Licenses TSHR Antibody to Yarrow for $1.4B in Graves’ Disease Deal

Fineline Cube Dec 16, 2025
Company Deals

uBriGene Partners with Circurna on circRNA Manufacturing for Global Trials

Fineline Cube Dec 16, 2025
Company Deals

Dren Bio, Sanofi Forge $1.8B B‑Cell Therapy Deal with US Co‑Promote Option

Fineline Cube Dec 16, 2025
Company Deals

Adaptive Licenses TCR Data to Pfizer in $890M Deal for Rheumatoid Arthritis

Fineline Cube Dec 16, 2025
Company Deals

Sobi Acquires Arthrosi for $1.5 Billion to Add Gout Drug to Portfolio

Fineline Cube Dec 15, 2025
Policy / Regulatory

FDA Removes Key RWE Limitation, Allowing Drug and Device Submissions Without Individual Patient Data

Fineline Cube Dec 16, 2025
Company Drug

Orelabrutinib First BTK Inhibitor to Hit Phase 3 in Lupus as InnoCare NMPA Filing Cleared

Fineline Cube Dec 16, 2025
Company Drug

ENHERTU Wins FDA Approval as First-Line HER2 Breast Cancer Therapy

Fineline Cube Dec 16, 2025
Company Deals

XWPharma Secures $205 M Valiloxybate Deal with Avadel

Fineline Cube Sep 8, 2025

China‑based XWPharma Ltd. announced today that it has entered into an exclusive licensing agreement with...

Policy / Regulatory

FDA Launches “Green List” to Shield U.S. Markets from Unsafe GLP‑1 APIs

Fineline Cube Sep 8, 2025

The U.S. Food and Drug Administration (FDA) today announced a new “green list” import alert...

Company Drug

InnoCare Pharma Secures Singapore HSA Approval for Orelabrutinib in Relapsed MZL

Fineline Cube Sep 8, 2025

Shanghai‑based InnoCare Pharma (HKG: 9969, SHA: 688428) announced on September 8, 2025 that its Bruton’s tyrosine kinase...

Company Drug

Regenelead Secures NMPA Approval for RGL‑305 Cell Therapy in Advanced Malignant Tumors

Fineline Cube Sep 8, 2025

On September 2, 2025, Shanghai‑based Regenelead announced that its internally developed cell‑therapy product RGL‑305 Injection received...

Company Drug

Takeda Secures FDA Approval for VONVENDI’s Expanded Use in Adult and Pediatric VWD

Fineline Cube Sep 8, 2025

Japan-based Takeda Pharmaceutical (TYO: 4502, NYSE: TAK) today confirmed that the U.S. Food and Drug...

Company Drug

QuantumPharm XtalPi Secures Phase I Approval for PEP08, a Next‑Generation PRMT5 Inhibitor

Fineline Cube Sep 8, 2025

Shenzhen-based QuantumPharm Inc., known as Xtalpi Inc. (HKG: 2228) announced a pivotal clinical milestone for...

Company Deals

Escugen and Huahui Health Form Exclusive Partnership to Develop First‑in‑Class ADC for Solid Tumors

Fineline Cube Sep 8, 2025

Shanghai‑based Escugen and Beijing‑headquartered Huahui Health have announced a global, exclusive cooperation agreement to develop...

Policy / Regulatory

NHSA Releases Draft Regulations to Tighten Medical Insurance Funds Oversight

Fineline Cube Sep 8, 2025

On September 7, 2025, China’s National Healthcare Security Administration (NHSA) issued the Draft Implementation Rules for the...

Company Deals

Gilead Terminates $2.3 B Collaboration With Kite Pharma Over Off‑the‑Shelf Cell Therapies

Fineline Cube Sep 8, 2025

US-based Gilead Sciences’ (NASDAQ: GILD) subsidiary Kite Pharma has officially ended its $2.3 billion collaboration with Shoreline...

Company Drug

Junshi Biosciences’ JS005 IL‑17A Antibody Shows Promise in Phase III Psoriasis Trial

Fineline Cube Sep 8, 2025

Shanghai Junshi Biosciences Co., Ltd. (HKG: 1877, SHA: 688180) announced that its proprietary recombinant humanized...

Company Drug

Hengrui’s RSS0393 PDE4 Inhibitor Approved for Atopic Dermatitis Clinical Trial

Fineline Cube Sep 5, 2025

Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276, HKG: 1276) announced that its proprietary topical RSS0393...

Company Drug

Hengrui’s HRS‑4729 GLP‑1 Triple Agonist Receives NMPA Approval for MASLD & MASH

Fineline Cube Sep 5, 2025

Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276, HKG: 1276) announced that its investigational drug HRS‑4729...

Company Drug

Innovent’s Xinbimin IGF‑1R Antibody Approved in Macau

Fineline Cube Sep 5, 2025

China-based Innovent Biologics Inc. (HKG: 1801) announced that the Macau Special Administrative Region drug authority...

Company Drug

TransThera Begins Phase II Tinengotinib Trial with Akeso Bispecifics for Advanced HCC

Fineline Cube Sep 5, 2025

TransThera Sciences (Nanjing) Inc. (HKG: 2617) announced the first patient dose in an open‑label, multi‑center...

Company Drug

Simcere Launches Quviviq, New Insomnia Therapy in China

Fineline Cube Sep 5, 2025

Jiangsu Simcere Pharmaceutical Co., Ltd. (HKG: 2096) announced the nationwide launch of its first prescription...

Company Deals

Hengrui Licenses HRS‑1893 to Braveheart Bio in $75 M Deal – Global Myosin Inhibitor

Fineline Cube Sep 5, 2025

Jiangsu Hengrui Pharmaceuticals Co., Ltd. (SHA: 600276, HKG: 1276) announced an exclusive licensing arrangement with...

Company Deals

Dongcheng Pharma to Spin‑Off Lannacheng for HK Main Board Listing – Radiopharma Focus

Fineline Cube Sep 5, 2025

Yantai Dongcheng Pharmaceutical Group Co., Ltd. (SHE: 002675) announced that it will spin off its...

Company Drug

Hengrui’s SHR‑A2009 ADC Gains NMPA Approval for HER3‑Targeted Tumor Therapy

Fineline Cube Sep 4, 2025

China‑based Jiangsu Hengrui Pharmaceuticals Co., Ltd. (HKG: 1276, SHA: 600276) announced that the China National Medical...

Company Drug

Haisco Pharmaceutical’s HSK47388 Gears Up for New Autoimmune Trial – NMPA Approval

Fineline Cube Sep 4, 2025

Haisco Pharmaceutical Group Co., Ltd. (SHE: 002653) announced that the National Medical Products Administration (NMPA)...

Company Drug

Boji Medical’s FCZR Approved for Otomycosis Trials – First Liquid Eardrop in China

Fineline Cube Sep 4, 2025

Boji Medical Technology Co., Ltd. (SHE: 300404) has secured approval from the National Medical Products...

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Recent updates

  • Orelabrutinib First BTK Inhibitor to Hit Phase 3 in Lupus as InnoCare NMPA Filing Cleared
  • Saizeng Medical Licenses TSHR Antibody to Yarrow for $1.4B in Graves’ Disease Deal
  • Zhicheng’s TAVR Robotic System Enters NMPA Innovation Pathway
  • ENHERTU Wins FDA Approval as First-Line HER2 Breast Cancer Therapy
  • FDA Removes Key RWE Limitation, Allowing Drug and Device Submissions Without Individual Patient Data
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

Orelabrutinib First BTK Inhibitor to Hit Phase 3 in Lupus as InnoCare NMPA Filing Cleared

Company Deals

Saizeng Medical Licenses TSHR Antibody to Yarrow for $1.4B in Graves’ Disease Deal

Company Medical Device

Zhicheng’s TAVR Robotic System Enters NMPA Innovation Pathway

Company Drug

ENHERTU Wins FDA Approval as First-Line HER2 Breast Cancer Therapy

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