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Company Deals

Gilead Sciences to Acquire Arcellx for $7.8B – Bolsters CAR‑T Pipeline with BCMA‑Targeted Anito‑cel

Fineline Cube Feb 24, 2026
Company Deals

Findcure Bio Raises $14.5 Million Series B to Advance Radiopharmaceutical Platform

Fineline Cube Feb 14, 2026
Company Deals

Siemens Healthineers Deepens Mayo Clinic Partnership on AI Neurology and Precision Oncology

Fineline Cube Feb 14, 2026
Company Deals

VivaVision Biotech Files Hong Kong IPO to Advance Ophthalmology Pipeline

Fineline Cube Feb 14, 2026
Company Deals

Genhouse Bio Partners with Gilead on $1.5 Billion Synthetic Lethal Cancer Project GH31

Fineline Cube Feb 14, 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FDA Issues Draft Guidance on Plausible Mechanism Framework – Accelerates Approval Pathway for Individualized Genetic Therapies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

Sichuan Biokin’s Iza‑Bren Hits PFS and OS Endpoints in Phase III TNBC Study – First Bispecific ADC to Show Dual Survival Benefit

Fineline Cube Feb 24, 2026
Company Drug

Sino Biopharma’s Benmelstobart Secures Fourth NMPA Approval for Stage III NSCLC – Expanding PD‑L1 Franchise in China

Fineline Cube Feb 14, 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

  • Trinomab’s Retavibart NDA Accepted by NMPA – First Long‑Acting RSV mAb for Infant Protection in China
  • Sichuan Biokin’s Iza‑Bren Hits PFS and OS Endpoints in Phase III TNBC Study – First Bispecific ADC to Show Dual Survival Benefit
  • FDA Issues Draft Guidance on Plausible Mechanism Framework – Accelerates Approval Pathway for Individualized Genetic Therapies
  • Gilead Sciences to Acquire Arcellx for $7.8B – Bolsters CAR‑T Pipeline with BCMA‑Targeted Anito‑cel
  • Pfizer Partners with Sciwind Biosciences for Ecnoglutide China Rights – $495M Deal Marks Metabolic Market Entry
Special Report 2025 Q1: U.S. Targets Chinese Pharma with 200% Tariffs—Will the Global Drug Market Collapse?

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You Missed

Others

Trinomab’s Retavibart NDA Accepted by NMPA – First Long‑Acting RSV mAb for Infant Protection in China

Company Drug

Sichuan Biokin’s Iza‑Bren Hits PFS and OS Endpoints in Phase III TNBC Study – First Bispecific ADC to Show Dual Survival Benefit

Policy / Regulatory

FDA Issues Draft Guidance on Plausible Mechanism Framework – Accelerates Approval Pathway for Individualized Genetic Therapies

Company Deals

Gilead Sciences to Acquire Arcellx for $7.8B – Bolsters CAR‑T Pipeline with BCMA‑Targeted Anito‑cel

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