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NMPA

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Company Drug

Clover Biopharmaceuticals’ SCB-2019 COVID-19 Vaccine Shows Strong Immune Response in Third Shot Study

Fineline Cube Jun 28, 2022

China-based Clover Biopharmaceuticals Ltd (HKG: 2197) has published clinical data for its COVID-19 vaccine candidate...

Policy / Regulatory

NHSA Releases Draft Proposals for NRDL Annual Renewal Process

Fineline Cube Jun 14, 2022

The National Healthcare Security Administration (NHSA) has formulated and released draft proposals for rules covering...

Policy / Regulatory

Enhancing Clinical Trial Success: CDE’s New Adaptive Design Framework Opens for Comment

Fineline Cube May 14, 2020

The newly proposed guidelines are designed to be applicable across a spectrum of confirmatory clinical...

Posts pagination

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Recent updates

  • Pfizer’s Hympavzi Wins FDA Priority Review for Pediatric Hemophilia Expansion
  • Zhongsheng Pharma Reports Positive Phase III Data for Onradivir Pediatric and Adolescent Influenza Trials
  • InnoCare Pharma’s ICP-538 Becomes First VAV1 Molecular Glue Degrader to Enter China Clinical Trials
  • Betta Pharma Secures NMPA Approval for Beizeting, First Domestic Pertuzumab Biosimilar in China
  • Kelun-Biotech’s Jiatailai Secures Fourth NMPA Approval for HR+/HER2- Breast Cancer Indication
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

Pfizer’s Hympavzi Wins FDA Priority Review for Pediatric Hemophilia Expansion

Company Drug

Zhongsheng Pharma Reports Positive Phase III Data for Onradivir Pediatric and Adolescent Influenza Trials

Company Drug

InnoCare Pharma’s ICP-538 Becomes First VAV1 Molecular Glue Degrader to Enter China Clinical Trials

Company Drug

Betta Pharma Secures NMPA Approval for Beizeting, First Domestic Pertuzumab Biosimilar in China

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