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FDA Issues Draft Guidance on Plausible Mechanism Framework – Accelerates Approval Pathway for Individualized Genetic Therapies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

Pfizer and Astellas’ Xtandi Shows Positive Results in Phase III EMBARK Study for Prostate Cancer

Fineline Cube Jul 14, 2025

Partners Pfizer (NYSE: PFE) and Astellas Pharma Inc. (TYO: 4503) announced positive topline results from...

Company Drug

Bayer’s Elinzanetant Granted UK Marketing Authorization for Menopause-Related Vasomotor Symptoms

Fineline Cube Jul 11, 2025

Germany’s Bayer (ETR: BAYN) this week announced that the UK Medicines and Healthcare products Regulatory...

Company Deals Drug

AbbVie Licenses IGI Therapeutics’ ISB 2001 for Oncology and Autoimmune Diseases

Fineline Cube Jul 11, 2025

US-based AbbVie (NYSE: ABBV) this week announced a licensing agreement with IGI Therapeutics SA, a...

Company Drug

Jiangsu Jibeier Receives NMPA Approval for Clinical Trials of JJH201601 Liposome in Advanced HNSCC

Fineline Cube Jul 11, 2025

China-based Jiangsu Jibeier Pharm Co., Ltd (SHA: 688566) announced that it has received clinical approval...

Company Drug

Fosun Pharmaceutical Launches Phase III Study for Fumaining in Pediatric Low-Grade Glioma

Fineline Cube Jul 11, 2025

Shanghai-based Fosun Pharmaceutical (Group) Co., Ltd (SHA: 600196, HKG: 2196) announced the initiation of a...

Company Drug

BeOne Medicines’ Tevimbra Approved by European Commission for Nasopharyngeal Carcinoma

Fineline Cube Jul 11, 2025

China-based BeOne Medicines Ltd. (NASDAQ: ONC, HKG: 6160, SHA: 688235) announced that it has received...

Company Medical Device

Johnson & Johnson MedTech Launches VARIPULSE Platform for Atrial Fibrillation in Asia-Pacific

Fineline Cube Jul 11, 2025

US major Johnson & Johnson MedTech announced the launch of its VARIPULSE Platform in the...

Company Deals

JCR Pharmaceuticals Signs Licensing Agreement with AstraZeneca’s Alexion for JUST-AAV Gene Therapy Platform

Fineline Cube Jul 11, 2025

Japan-based JCR Pharmaceuticals Co., Ltd. (TYO: 4552) announced a licensing agreement with UK-based AstraZeneca’s (NASDAQ:...

Company Drug

Zhimeng Biopharma’s CB03-154 Receives CDE Approval for ALS Phase II/III Clinical Study

Fineline Cube Jul 11, 2025

China-based Shanghai Zhimeng Biopharma, Inc. is set to carry out a Phase II/III clinical study...

Policy / Regulatory

NHSA Finalizes 2025 Drug Catalog Adjustment Plan with Minimal Changes from Draft

Fineline Cube Jul 11, 2025

The National Healthcare Security Administration (NHSA) this week issued the finalized “2025 National Basic Medical...

Company Drug

MSD’s Once-Daily HIV-1 Therapy Doravirine/Islatravir NDA Accepted by FDA for Review

Fineline Cube Jul 11, 2025

Merck, Sharp & Dohme (MSD, NYSE: MRK) announced that the U.S. Food and Drug Administration...

Company Drug

Zelgen’s ZG006 Receives Breakthrough Therapy Designation for Advanced Small Cell Lung Cancer

Fineline Cube Jul 11, 2025

China-based Suzhou Zelgen Biopharmaceuticals Co., Ltd (SHA: 688266) announced that it has received breakthrough therapy...

Company Drug

Cosunter’s GST-HG131 Granted Breakthrough Therapy Designation for HBV Treatment in China

Fineline Cube Jul 11, 2025

China-based Fujian Cosunter Pharmaceutical Co., Ltd (SHE: 300436) announced that it has received breakthrough therapy...

Company Drug

Ascentage Pharma’s Lisaftoclax Receives NMPA Approval for CLL/SLL Treatment

Fineline Cube Jul 11, 2025

China-based Ascentage Pharma (NASDAQ: AAPG, HKG: 6855) announced that it has received conditional marketing approval...

Company Drug

Allist’s Furmonertinib Granted Priority Review for EGFR Exon 20 NSCLC in China

Fineline Cube Jul 11, 2025

Shanghai-based biotech Allist Pharmaceuticals Co., Ltd. (SHA: 688578) announced that its Category 1 small molecule...

Company Drug

HKYM Biopharma’s KM1 Receives NMPA Green-Light for Phase Ib/II Study in Advanced Solid Tumors

Fineline Cube Jul 11, 2025

Shenzhen-based oncolytic virus specialist HKYM Biopharma has announced receiving the green-light from the National Medical...

Company Drug

United Laboratories Receives FDA Approval for Clinical Study of UBT37034 in Overweight/Obesity Treatment

Fineline Cube Jul 11, 2025

Hong Kong-based United Laboratories International Holdings Ltd (HKG: 3933) has announced that it has received...

Company Drug

CStone Pharmaceuticals Receives NMPA Approval for Local Production of Gavreto in China

Fineline Cube Jul 10, 2025

China-based CStone Pharmaceuticals (HKG: 2616) has announced that it has received approval from the National...

Company Deals

Biocytogen and BeOne Medicines Deepen Partnership with Global Antibody Licensing Agreement

Fineline Cube Jul 10, 2025

China’s Biocytogen Pharmaceuticals (Beijing) Co., Ltd. (HKG: 2315) has announced a global antibody molecule licensing...

Company Drug

Eli Lilly’s Kisunla (Donanemab) Receives FDA Label Update with New Dosing Schedule for Alzheimer’s Treatment

Fineline Cube Jul 10, 2025

US pharmaceutical giant Eli Lilly & Co. (NYSE: LLY) has announced that the US Food...

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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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