Drug

Patronus Biotech Secures Ethics Approval to Launch Phase I Trials of Three Multi‑Stage U‑VLP Malaria Vaccine Candidates – First‑in‑Human Study of LYB014, LYB017 and LYB027 Set to Begin in Australia
Clinical trial approval / initiationPatronus Biotech

Patronus Biotech Secures Ethics Approval to Launch Phase I Trials of Three Multi‑Stage U‑VLP Malaria Vaccine Candidates – First‑in‑Human Study of LYB014, LYB017 and LYB027 Set to Begin in Australia

Patronus Biotech Co., Ltd. announced that its three multi‑stage novel U‑VLP malaria vaccine candidates – LYB014, LYB017 and LYB027 – have been approved by the Bellberry Human Research Ethics Committee…

Takeda's Adcetris Approved by NMPA for First-Line CD30-Positive PTCL – China's First and Only Targeted Therapy in Combination With CHP for sALCL and Other CD30-Positive Peripheral T-Cell Lymphomas

Takeda’s Adcetris Approved by NMPA for First-Line CD30-Positive PTCL – China’s First and Only Targeted Therapy in Combination With CHP for sALCL and Other CD30-Positive Peripheral T-Cell Lymphomas

NMPA Approves New Indication for J&J's Tecvayli in Relapsed or Refractory Multiple Myeloma – Bispecific BCMA/CD3 Antibody Moves to First Relapse After ≥1 Prior Line

NMPA Approves New Indication for J&J’s Tecvayli in Relapsed or Refractory Multiple Myeloma – Bispecific BCMA/CD3 Antibody Moves to First Relapse After ≥1 Prior Line

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BioNTech and BMS Reveal Promising Interim Results for Pumitamig in ES‑SCLC
BioNTechBMS

BioNTech and BMS Reveal Promising Interim Results for Pumitamig in ES‑SCLC

Summit Therapeutics Presents 2025 HARMONi Study Results at World Lung Cancer Conference
CancerClinical trial results

Summit Therapeutics Presents 2025 HARMONi Study Results at World Lung Cancer Conference

FibroX Therapeutics Secures IND Approval for FibroCell in Lumbar Disc Degeneration
Cell-therapyClinical trial approval / initiation

FibroX Therapeutics Secures IND Approval for FibroCell in Lumbar Disc Degeneration

NMPA Unveils 30‑Working‑Day Pathway to Accelerate Innovative Drug Trials
CDENMPA

NMPA Unveils 30‑Working‑Day Pathway to Accelerate Innovative Drug Trials

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