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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
Company Deals

Kyinno Biotechnology Closes RMB 250M Series B for Bispecific Antibody Pipeline

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

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

Fineline Cube Dec 16, 2025
Company Drug

Sanofi’s Tolebrutinib Fails Phase 3 PPMS Endpoint, Halting Registration Plans

Fineline Cube Dec 16, 2025
Company

Abbott Reports Q2 2025 Sales of USD 11.14 Billion, Led by Medical Devices Growth

Fineline Cube Jul 22, 2025

Abbott (NYSE: ABT) reported global sales of USD 11.14 billion for the second quarter of...

Company Drug

DualityBio’s Next-Generation HER3 ADC DB-1310 Granted FDA Fast Track Designation

Fineline Cube Jul 22, 2025

Duality Biologics (HKG: 9606) announced that the US Food and Drug Administration (FDA) has granted...

Company Deals

Shanghai Pharma and Cutia Therapeutic Collaborate on Codon Biopharma’s Innovative Drug Distribution

Fineline Cube Jul 22, 2025

China’s Shanghai Pharmaceuticals Holding Co., Ltd (SPH, HKG: 2607, SHA: 601607) announced the signing of...

Company Drug

Bio-Thera’s BAT4406F Gets NMPA Nod for MCD and FSGS Clinical Trials

Fineline Cube Jul 22, 2025

Guangzhou-based Bio-Thera Solutions (SHA: 688177) announced that its investigational drug, BAT4406F injection, has received approval...

Company Drug

Huadong Medicine Receives NMPA Approval for HDM2012 Clinical Trials in Advanced Solid Tumors

Fineline Cube Jul 21, 2025

China-based Huadong Medicine Co., Ltd (SHE: 000963) announced that it has received clinical trial approval...

Company Deals Medical Device

Optoseeker Biotech and BioMap Collaborate to Accelerate Antibody Therapeutics Development

Fineline Cube Jul 21, 2025

Optoseeker Biotech, a leader in advanced life science instrumentation, and BioMap, a pioneer in life...

Company Medical Device

Wondfo Biotech’s MSI Detection Kit Granted NMPA Marketing Clearance

Fineline Cube Jul 21, 2025

Guangzhou-based Wondfo Biotech (SHE: 300482) announced that the National Medical Products Administration (NMPA) has granted...

Company Medical Device

Zhongke Yian Receives NMPA Approval for Innovative Sirolimus-Eluting Coronary Stent

Fineline Cube Jul 21, 2025

ZhongKe Yian Medical Technology (Beijing) Co., Ltd. has secured approval from China’s National Medical Products...

Company Drug

NMPA Approves World’s First Plant-Based Human Albumin for Liver Cirrhosis Treatment

Fineline Cube Jul 21, 2025

China’s National Medical Products Administration (NMPA) has approved the world’s first plant-based human albumin, a...

Company Medical Device

KANTE Biotech’s Yilijia Wins NMPA Category III License for Pancreatic Cancer Early Detection

Fineline Cube Jul 21, 2025

KANTE (Shenzhen) Biotechnology Co., Ltd (“Kante-bio”) announced that it has received a Category III medical...

Company

WuXi Biologics Passes FDA Pre-Approval Inspection with Zero Critical Findings

Fineline Cube Jul 21, 2025

WuXi Biologics (HKG: 2269) announced on July 21, 2025, that five of its manufacturing facilities...

Company Drug

Jumpcan Pharmaceutical’s Jike Shu Approved by NMPA for Influenza A and B Treatment

Fineline Cube Jul 21, 2025

Shanghai-based Jumpcan Pharmaceutical (SHA: 600566) announced that its independently developed Class 1 innovative drug, Jike...

Policy / Regulatory

CDE Seeks Feedback on 96th Batch of Chemical Generic Drug Reference Standards

Fineline Cube Jul 21, 2025

China’s Center for Drug Evaluation (CDE) is currently seeking public feedback on the 96th batch...

Company Drug

Novo Nordisk’s Ozempic Approved for Kidney Protection in China, Pioneering Glycemic and Renal Control

Fineline Cube Jul 21, 2025

The National Medical Products Administration has granted approval to Novo Nordisk’s (NYSE: NVO) once-weekly semaglutide...

Company Deals

Shanghai Wankexin Biotech to Acquire Stake in Chengdu Kanghua Biological for RMB 1.851 Billion

Fineline Cube Jul 21, 2025

Shanghai Wankexin Biotechnology Partnership Enterprise (Limited Partnership) (“Wankexin Biotech”), a subsidiary of the Shanghai Biomedicine...

Policy / Regulatory

Hebei Implements Separate Payment for 57 Negotiated Drugs Starting August 1, 2025

Fineline Cube Jul 21, 2025

The Hebei provincial healthcare security administration has issued the “Notice on Improving the Separate Payment...

Company Deals

Bayer and JD Health Collaborate on Dulcolax-Lactulose to Expand China’s Digestive-Health Market

Fineline Cube Jul 21, 2025

Bayer (ETR: BAYN) and JD Health (HKG: 6618) have launched Dulcolax-branded lactulose in a pioneering...

Company Drug

Sarepta Therapeutics Announces 500 Employee Layoffs After FDA Elevidys Trial Suspension

Fineline Cube Jul 21, 2025

US-based Sarepta Therapeutics, a subsidiary of Sanofi (NASDAQ: SNY), announced the layoff of approximately 500...

Company Deals

VivaVision Biotech Closes D2+ Funding Round, Advancing Ophthalmic Therapies

Fineline Cube Jul 21, 2025

VivaVision Biotech recently announced the successful closing of its D2+ funding round, raising 140 million...

Company Drug

Youcare Pharma Subsidiary Gains NMPA Clearance for Phase I Study of siRNA Hypertension Drug YKYY029

Fineline Cube Jul 18, 2025

China-based Youcare Pharma (SHA: 688658) announced that its subsidiary Youcare InnoTech and partner Hangzhou Tianlong...

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Recent updates

  • 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
  • Sanofi’s Tolebrutinib Fails Phase 3 PPMS Endpoint, Halting Registration Plans
  • Konruns Doses First Patient in Phase 2 Esophageal Cancer Trial for KC1036
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 Medical Device

Zhicheng’s TAVR Robotic System Enters NMPA Innovation Pathway

Company Drug

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

Policy / Regulatory

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

Company Drug

Sanofi’s Tolebrutinib Fails Phase 3 PPMS Endpoint, Halting Registration Plans

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