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Sichuan Kelun-Biotech Reports H1 Revenue Drop, Advances Key Drug Commercialization
Company

Sichuan Kelun-Biotech Reports H1 Revenue Drop, Advances Key Drug Commercialization

August 20, 2025
WuXi Biologics Reports 16.1% Revenue Growth in H1 2025, Launches WuXiHigh 2.0 Platform
Company

WuXi Biologics Reports 16.1% Revenue Growth in H1 2025, Launches WuXiHigh 2.0 Platform

August 20, 2025
RemeGen's RC148 Granted Breakthrough Therapy Designation for NSCLC Treatment
CompanyDrug

RemeGen’s RC148 Granted Breakthrough Therapy Designation for NSCLC Treatment

August 20, 2025
Shandong Lukang's CIGB-814 Starts Phase 1 Trial for Rheumatoid Arthritis Treatment
CompanyDrug

Shandong Lukang’s CIGB-814 Starts Phase 1 Trial for Rheumatoid Arthritis Treatment

August 20, 2025
HutchMed Completes Patient Enrollment for Orpathys and Tagrisso Combination Study
CompanyDrug

HutchMed Completes Patient Enrollment for Orpathys and Tagrisso Combination Study

August 20, 2025
Sino Biopharmaceutical Reports 10.7% Revenue Growth and 140.2% Profit Surge in H1 2025
Company

Sino Biopharmaceutical Reports 10.7% Revenue Growth and 140.2% Profit Surge in H1 2025

August 19, 2025
Kangtai Biological Gains NMPA Approval for Trivalent Influenza Vaccine Clinical Trial
CompanyDrug

Kangtai Biological Gains NMPA Approval for Trivalent Influenza Vaccine Clinical Trial

August 19, 2025
Zhifei Biological's Adult and Adolescent DTaP Vaccine Gains NMPA Trial Approval
CompanyDrug

Zhifei Biological’s Adult and Adolescent DTaP Vaccine Gains NMPA Trial Approval

August 19, 2025
RemeGen Inks Licensing Deal With Santen China for RC28-E Eye Disease Drug
CompanyDigital

RemeGen Inks Licensing Deal With Santen China for RC28-E Eye Disease Drug

August 19, 2025
MicroPort CardioFlow's Alwide Plus Wins EU CE Mark for Heart Valve Procedures
CompanyMedical Device

MicroPort CardioFlow’s Alwide Plus Wins EU CE Mark for Heart Valve Procedures

August 19, 2025
Mabwell's Innovative CDH17-Targeted ADC 7MW4911 Receives FDA Clinical Trial Approval
CompanyDrug

Mabwell’s Innovative CDH17-Targeted ADC 7MW4911 Receives FDA Clinical Trial Approval

August 19, 2025
Hengrui Pharma's Hetrombopag Olamine Accepted by NMPA for Chemotherapy-Induced Thrombocytopenia
CompanyDrug

Hengrui Pharma’s Hetrombopag Olamine Accepted by NMPA for Chemotherapy-Induced Thrombocytopenia

August 19, 2025
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Insight,  China's Pharmaceutical Industry

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