Zanidatamab Doubles Survival in HER2-Positive Gastric Cancer Trial
Zanidatamab doubles survival in HER2-positive gastric cancer trial, achieving 29.7 months median OS versus 15.8 months with trastuzumab in...
Adaptive Clinical Trial Design Adaptive Trial Design Addiction Psychiatry AI in Clinical Trials alcohol use disorder Alzheimer's Disease Article Clinical Operations Clinical Research Clinical Trial Design Clinical Trial Operations Clinical Trial Ops Brief Clinical Trials CLINOPS WATCHDOG CNS Drug Development CNS Trials Conference Coverage CRO Consolidation Decentralized Clinical Trials Digital Health Technologies dual diagnosis eClinical Tech News eClinical Technology EMA Executive Interviews FDA Enforcement FDA Guidance FDA Real-World Evidence FDA Regulation FDA Regulatory Strategy GCP Compliance GLP-1 Receptor Agonists Ketamine Therapy Oncology Trials Opinion Parkinson's Disease Platform Trials Psilocybin MDMA Psychedelic Clinical Trials PSYCH PULSE Real-World Evidence site activation Site Operations study startup Treatment-Resistant Depression
Zanidatamab doubles survival in HER2-positive gastric cancer trial, achieving 29.7 months median OS versus 15.8 months with trastuzumab in...
TG Therapeutics' ublituximab shows bioequivalent exposure in single-dose trial, potentially simplifying MS treatment initiation with reduced clinic visits.
Zumilokibart achieves EASI-75 target in Phase 2 atopic dermatitis trial with fewer injections than dupilumab and lower conjunctivitis rates.
Kordata Dynamics launches an AI model built for real-time neural data in trials. Here's what it means for site...
Novartis presents eGFR slope data for IgAN kidney disease treatments at ERA 2026, comparing complement inhibition and endothelin receptor...
FDA Approves DECNUPAZ for blastic plasmacytoid dendritic cell neoplasm, achieving 69.7% composite complete response in newly diagnosed patients.
Utah's clinical AI sandbox and the FDA's 1,451 AI device authorizations reveal a structural oversight gap—states are building what...
Aktis Oncology's AKY-2519 demonstrates lower salivary gland toxicity compared to approved PSMA agents in first-in-human dosimetry study.
TaiMed completes Phase 2b enrollment for TMB-365/380, a dual antibody HIV therapy dosed every two months without pre-screening requirements.
Tedopi Plus Pembrolizumab reduces progression or death risk by 47% versus supportive care in platinum-sensitive recurrent ovarian cancer.