Celcuity to Present Updated VIKTORIA-1 Data at SABCS 2025
No new efficacy numbers were disclosed, but Celcuity will present updated subgroup and safety results from the randomized Phase...
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 Trial Quality Clinical Trials CLINOPS WATCHDOG CNS Drug Development CNS Trials Conference Coverage 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
No new efficacy numbers were disclosed, but Celcuity will present updated subgroup and safety results from the randomized Phase...
FibroBiologics has repaid all amounts outstanding under its Yorkville-issued convertible promissory notes, removing the prospect of further conversions into...
Tangram Therapeutics has submitted a Clinical Trial Application to the UK MHRA to begin a Phase 1/2 study of...
Tiziana Life SciencesLife Sciences’ intranasal anti-CD3 antibody, foralumab, has been accepted into the ALS MyMatch Program at the Healey...
BriaCell will present survival readouts from its Phase 2 study of the allogeneic whole cell vaccine Bria-IMT and new...
Kymera has begun dosing in BROADEN2, a 16-week, randomized, double-blind, placebo-controlled Phase 2b study of KT-621 in moderate to...
Macomics has validated its ENIGMAC macrophage discovery platform in antifibrotic biology, completing pooled and arrayed CRISPR-based gene modulation screens...
Junshi Biosciences reported that its Phase 3 JS001sc-002-III-NSCLC study met primary endpoints, showing non-inferior drug exposure for subcutaneous toripalimab...
In this interview, Vinita Navadgi, Sr. Director, Digital Patient Suite, IQVIA, shares a practical, thought-leading view on AI-driven electronic...
Gelteq reported a 38–45% increase in AUC and a markedly higher Cmax versus a marketed reference antihistamine in a...