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Company Deals

Boji Medical Sells Fluconazole Ear Drops Technology to Chengdu Pusch for $2M

Fineline Cube Apr 22, 2026
Company Deals

Novabio Therapeutics and OBiO Tech Strengthen Partnership to Advance Treg Cell Therapies for Neurodegenerative Diseases

Fineline Cube Apr 22, 2026
Company Deals

InxMed Limited Files for Hong Kong IPO with Near-Commercial FAK Inhibitor Ifebemtinib

Fineline Cube Apr 22, 2026
Company Deals

NeuroGen Pharma Secures Exclusive China Rights to Teva’s Ajovy – World’s First Dual-Indication CGRP Antagonist for Migraine Prevention

Fineline Cube Apr 22, 2026
Company Deals

Eli Lilly to Acquire Kelonia Therapeutics for $7 Billion to Secure In Vivo CAR-T Platform Targeting Multiple Myeloma

Fineline Cube Apr 21, 2026
Policy / Regulatory

NMPA Suspends Colchicine API Imports from Indian Manufacturers Alkaloids Bioactives and Alchem International Over Change Management Violations

Fineline Cube Apr 23, 2026
Company Drug

FDA Approves Sanofi-Regeneron’s Dupilumab for Pediatric Chronic Spontaneous Urticaria in Children Aged 2–11 Years

Fineline Cube Apr 23, 2026
Company Drug

China’s CDE Releases 106th Batch of Chemical Generic Reference Preparations with 27 New Specifications and Updated Guidelines

Fineline Cube Apr 23, 2026
Company

Bio-Bank Corp. Aims for HKEX IPO with Focus on PDGF Drug Development

Fineline Cube May 7, 2024

B&K Corporation Limited, known as Bio-Bank Corp., has recently filed an initial public offering (IPO)...

Policy / Regulatory

China Upgrades Midazolam to Category I Psychotropic Drug List in Regulatory Rescheduling

Fineline Cube May 7, 2024

In a joint notification, the National Medical Products Administration (NMPA), Ministry of Public Security, and...

Company Drug

Merus’s Zenocutuzumab Receives Priority Review Status from FDA for Lung and Pancreatic Cancer Indications

Fineline Cube May 7, 2024

Dutch biotechnology company Merus (NASDAQ: MRUS) has announced that the US Food and Drug Administration...

Policy / Regulatory

Lei Haichao Takes Over as Party Secretary of China’s National Health Commission

Fineline Cube May 7, 2024

The National Health Commission (NHC) of China has undergone a leadership change, with Lei Haichao...

Company Drug

Betta Pharmaceuticals Files for Market Approval of CDK4/6 Inhibitor BPI-16350 in China

Fineline Cube May 7, 2024

Betta Pharmaceuticals Co., Ltd (SHE: 300558), a Chinese pharmaceutical company, has announced that it has...

Company Drug

Tonghua Dongbao Pharmaceuticals Commences Phase IIa Trial for Dual-Targeted Gout Drug Candidate

Fineline Cube May 7, 2024

Tonghua Dongbao Pharmaceuticals (SHA: 600867), a China-based pharmaceutical company, has announced that the first patient...

Company Policy / Regulatory

BIO Surveys Members on China-CDMO Dependence Amid BioSecurity Bill Deliberations

Fineline Cube May 7, 2024

The Biotechnology Innovation Organization (BIO), a prominent US industry trade group, is conducting a survey...

Company Drug

Henlius’ HER2 Dual-Targeted Therapy Gets Green Light for Global Phase III Trial by FDA

Fineline Cube May 7, 2024

Shanghai Henlius Biotech Co., Ltd (HKG: 2696) has announced that it has received approval from...

Company Drug

Jacobio Pharma Applies for Approval of KRAS G12C Inhibitor Gecirasib in China

Fineline Cube May 7, 2024

Jacobio Pharma (HKG: 1167), a China-based biopharmaceutical company, has announced the submission of a New...

Company Drug

China’s CDE Gives Tacit Approval to Keymed Biosciences’ Alzheimer’s Drug CM383 for Clinical Trials

Fineline Cube May 7, 2024

The Center for Drug Evaluation (CDE) has indicated on its website that China-based Keymed Biosciences...

Company Deals

Biocytogen and BioCopy AG Collaborate on TCR-Mimic Antibody Development for Cancer Therapies

Fineline Cube May 7, 2024

Biocytogen Pharmaceuticals (Beijing) Co., Ltd (HKG: 2315), a China-based biopharmaceutical company, has announced an evaluation...

Policy / Regulatory

CDE Seeks Public Comment on Latest Generic Chemical Reference Preparations

Fineline Cube May 7, 2024

The Center for Drug Evaluation (CDE), China’s regulatory body, is currently seeking public feedback on...

Company

GSK’s Q1 2024 Results Beat Forecasts with 10% YOY Revenue Increase; Upgrades Full-Year Outlook

Fineline Cube May 7, 2024

GSK plc (NYSE: GSK), the UK pharmaceutical giant, announced its financial results for the first...

Company

Eli Lilly & Co. Raises Full-Year Guidance on Strength of Q1 2024 Results and Production Expansion

Fineline Cube May 7, 2024

Eli Lilly & Co. (NYSE: LLY) has reported financial results for the first quarter of...

Company

Pfizer Appoints Citigroup’s Andrew Baum as Executive Vice-President for Strategy and Innovation

Fineline Cube May 7, 2024

Pfizer Inc. (NYSE: PFE) has announced the appointment of Andrew Baum, M.D., to serve as...

Company Drug

EyePoint Pharmaceuticals’ Durvayu Fails to Meet Primary Endpoint in NPDR Trial

Fineline Cube May 7, 2024

EyePoint Pharmaceuticals Inc., (NASDAQ: EYPT) has announced that its drug candidate Durvayu (vorolanib intravitreal insert;...

Company

Pfizer’s Q1 2024 Results Highlight Robust Portfolio Growth and Profitability

Fineline Cube May 6, 2024

Pfizer Inc. (NYSE: PFE) saw its share price surge over 5% following the release of...

Company Policy / Regulatory

US Legislature Reviews BioSecurity Bill to Sever Biotech Industry Ties with Chinese Companies

Fineline Cube May 6, 2024

On May 15, 2024, the US House Oversight Committee is set to review a “BioSecurity”...

Company Drug

Kelun-Biotech’s RET Inhibitor A400 Advances to Phase II Trial with FDA Approval

Fineline Cube May 6, 2024

Sichuan Kelun Pharmaceutical Co., Ltd (SHE: 002422), a Chinese pharmaceutical company, has announced that its...

Company Drug

Everest Medicines’ Nefecon Secures Market Approval for IgAN Treatment in Hong Kong

Fineline Cube May 6, 2024

Everest Medicines (HKG: 1952), a China-based pharmaceutical company, announced that it has received market approval...

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Recent updates

  • FDA Approves Sanofi-Regeneron’s Dupilumab for Pediatric Chronic Spontaneous Urticaria in Children Aged 2–11 Years
  • China’s CDE Releases 106th Batch of Chemical Generic Reference Preparations with 27 New Specifications and Updated Guidelines
  • FDA Extends Review Timeline for Sanofi’s Sarclisa Subcutaneous Formulation by Three Months; New Decision Date Set for July 23, 2026
  • NMPA Suspends Colchicine API Imports from Indian Manufacturers Alkaloids Bioactives and Alchem International Over Change Management Violations
  • Merck’s Idvynso Gains FDA Approval as Novel Dual-Drug HIV Treatment
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 Sanofi-Regeneron’s Dupilumab for Pediatric Chronic Spontaneous Urticaria in Children Aged 2–11 Years

Company Drug

China’s CDE Releases 106th Batch of Chemical Generic Reference Preparations with 27 New Specifications and Updated Guidelines

Company Drug

FDA Extends Review Timeline for Sanofi’s Sarclisa Subcutaneous Formulation by Three Months; New Decision Date Set for July 23, 2026

Policy / Regulatory

NMPA Suspends Colchicine API Imports from Indian Manufacturers Alkaloids Bioactives and Alchem International Over Change Management Violations

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