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Company Deals

SSY Group Secures Global Rights to Pediatric Antispasmodic and COPD Drugs from Xinzheng Heying – Full IP Transfer in Category 2.2 and 2.3 Assets

Fineline Cube Jun 5, 2026
Company Deals

Lonza and Stipple Bio Forge Strategic ADC Partnership – Combining Epitope Discovery with Glyco Connect Platform for Next-Generation Oncology Therapies

Fineline Cube Jun 5, 2026
Company Deals

Gilead and Lakefront Complete $1.675B Acquisition of Ouro Medicines – Securing BCMAxCD3 T Cell Engager for Autoimmune Diseases

Fineline Cube Jun 5, 2026
Company Deals

Pfizer Licenses Chai Discovery’s AI Platform for Drug Discovery – Gains Early Access to Breakthrough Chai-3 Model for Antibody Design

Fineline Cube Jun 5, 2026
Company Deals

Everest Medicines Secures Asia-Pacific Rights to Mabworks’ Obexelimab β in $30.9M Deal – First-in-Class CD20 Antibody for NMOSD

Fineline Cube Jun 5, 2026
Policy / Regulatory

China’s NHC Releases Sixth Pediatric Drug Priority List – 27 Varieties Including Emicizumab, Pembrolizumab, and Omalizumab Targeted for Development

Fineline Cube Jun 5, 2026
Company Drug

Guangzhou Lupeng’s Rocbrutinib Receives NMPA Priority Approval for Relapsed/Refractory Mantle Cell Lymphoma – Fourth-Generation BTK Inhibitor Shows 63.9% Response Rate

Fineline Cube Jun 5, 2026
Company Drug

Sichuan Biokin Receives NMPA Go-Ahead for BL-M08D1 Bispecific Antibody in DLBCL Combination Therapy – ADC Leverages Proven BL-B01D1 Platform

Fineline Cube Jun 5, 2026
Policy / Regulatory

CDE Releases Draft Guidelines for Tumor Therapeutic Vaccine Clinical Trials

Fineline Cube Oct 12, 2022

The Center for Drug Evaluation (CDE) has released the “Tumor Therapeutic Vaccines Clinical Trial Technical...

Company Deals

SprintRay Raises Over USD 100M in Series D Financing for Dental 3D Printing

Fineline Cube Oct 12, 2022

Zhejiang-based SprintRay Co., a one-stop digital chair side solution provider for dental institutions, has reportedly...

Company Drug

Pfizer’s Zavicefta Approved in China for Pediatric Complex Intra-Abdominal Infections

Fineline Cube Oct 11, 2022

US-based pharmaceutical giant Pfizer (NYSE: PFE) has announced that it has received market approval from...

Company Drug

HutchMed Initiates Phase II/III Study of Sovleplenib for Warm AIHA

Fineline Cube Oct 11, 2022

China-based Hutchison China Meditech (HutchMed; NASDAQ: HCM, HKG: 0013) has announced the initiation of a...

Company Deals

Harbour BioMed Licenses Batoclimab to CSPC’s NBP Pharma for Greater China

Fineline Cube Oct 11, 2022

Harbour BioMed (HKG: 2142), a biotech company operating out of the United States, the Netherlands,...

Company Drug

Guangdong Zhongsheng Receives USPTO Patent for FGFR4 Inhibitor ZSP1241

Fineline Cube Oct 11, 2022

China-based Guangdong Zhongsheng Pharmaceutical Co., Ltd (SHE: 002317) has announced receiving a patent award from...

Company Drug

Simcere Completes Enrollment for Phase III Study of CDK4/6 Inhibitor in mTNBC

Fineline Cube Oct 11, 2022

China-based Simcere Pharmaceutical Group (HKG: 2096) has announced the completion of first-line enrollment for its...

Company Drug

Hengrui Medicine’s Pyrotinib Filing Accepted for Review by NMPA

Fineline Cube Oct 11, 2022

China-based Jiangsu Hengrui Medicine Co., Ltd (SHA: 600276) has announced that its supplementary market filing...

Company Deals

China Resources Partners with Fosun Pharma to Expand Global Healthcare Footprint

Fineline Cube Oct 11, 2022

China Resources (Holdings) Co. Ltd (HKG: 3320) has entered into a strategic partnership with compatriot...

Company Drug

NMPA Approves JW Therapeutics’ Carteyva for Recurrent Follicular Lymphoma

Fineline Cube Oct 10, 2022

The National Medical Products Administration (NMPA) has granted another indication approval to China-based JW Therapeutics’...

Company Drug

Innovent’s Cyramza Gains NMPA Approval for Hepatocellular Carcinoma

Fineline Cube Oct 10, 2022

Innovent Biologics Inc. (HKG: 1801) has announced that the supplementary Biologic License Application (sBLA) for...

Company Drug

Sciwind Biosciences Initiates US Phase I Study for GLP-1 Agonist XW014

Fineline Cube Oct 10, 2022

China-based Sciwind Biosciences Co., Ltd has announced the initiation and first patient dosing of a...

Company Deals

Fujian Cosunter to Acquire UDCA Capsules Technology from Ruitailai

Fineline Cube Oct 10, 2022

China-based Fujian Cosunter Pharmaceutical Co., Ltd (SHE: 300436) has announced plans to enter into a...

Company Drug

Fujian Cosunter Doses First Patient in Phase I Study of COVID-19 Drug GST-HG171

Fineline Cube Oct 10, 2022

China-based Fujian Cosunter Pharmaceutical Co., Ltd (SHE: 300436) has announced that the first patient has...

Company Drug

Salubris Pharmaceuticals’ First-in-Class Anti-Tumor Drug SAL008 Accepted by NMPA

Fineline Cube Oct 10, 2022

China’s Shenzhen Salubris Pharmaceuticals Co., Ltd (SHE: 002294) has announced that a clinical trial filing...

Company Drug

Roche’s Subcutaneous Herceptin Approved in China for HER2-Positive Breast Cancer

Fineline Cube Oct 10, 2022

Swiss pharmaceutical giant Roche’s (SWX: ROG) Herceptin (trastuzumab, subcutaneous injection) has been approved in China...

Policy / Regulatory

CDE Releases 63rd Batch of Chemical Generic Reference Preparations

Fineline Cube Oct 10, 2022

The Center for Drug Evaluation (CDE) has released the 63rd batch of chemical generic reference...

Policy / Regulatory

Jiangsu Launches Sunshine Procurement Platform for Drugs and Medical Consumables

Fineline Cube Oct 10, 2022

Jiangsu province has launched its drugs and medical consumables sunshine procurement services website, providing a...

Company Drug

Merck’s Keytruda Gains 9th Indication Approval in China for Hepatocellular Carcinoma

Fineline Cube Oct 10, 2022

US major Merck Sharp & Dohme’s (MSD, NYSE: MRK) programmed death-1 (PD-1) inhibitor Keytruda (pembrolizumab)...

Company Deals

Convalife and Jointown Partner for Global Drug Development and Commercialization

Fineline Cube Oct 9, 2022

Shanghai-based Convalife Pharmaceuticals has entered into a strategic partnership with fellow Chinese firm Jointown Pharmaceutical...

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Recent updates

  • Guangzhou Lupeng’s Rocbrutinib Receives NMPA Priority Approval for Relapsed/Refractory Mantle Cell Lymphoma – Fourth-Generation BTK Inhibitor Shows 63.9% Response Rate
  • China’s NHC Releases Sixth Pediatric Drug Priority List – 27 Varieties Including Emicizumab, Pembrolizumab, and Omalizumab Targeted for Development
  • Sichuan Biokin Receives NMPA Go-Ahead for BL-M08D1 Bispecific Antibody in DLBCL Combination Therapy – ADC Leverages Proven BL-B01D1 Platform
  • Mabwell Bioscience Secures NMPA Clinical Approval for 9MW5211 in Inflammatory Bowel Disease – Highly Specific Depleting Antibody Targets Pathogenic Immune Cells
  • SSY Group Secures Global Rights to Pediatric Antispasmodic and COPD Drugs from Xinzheng Heying – Full IP Transfer in Category 2.2 and 2.3 Assets
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

Guangzhou Lupeng’s Rocbrutinib Receives NMPA Priority Approval for Relapsed/Refractory Mantle Cell Lymphoma – Fourth-Generation BTK Inhibitor Shows 63.9% Response Rate

Policy / Regulatory

China’s NHC Releases Sixth Pediatric Drug Priority List – 27 Varieties Including Emicizumab, Pembrolizumab, and Omalizumab Targeted for Development

Company Drug

Sichuan Biokin Receives NMPA Go-Ahead for BL-M08D1 Bispecific Antibody in DLBCL Combination Therapy – ADC Leverages Proven BL-B01D1 Platform

Company Drug

Mabwell Bioscience Secures NMPA Clinical Approval for 9MW5211 in Inflammatory Bowel Disease – Highly Specific Depleting Antibody Targets Pathogenic Immune Cells

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