Cancer Drug Destiny: Bicycle Toxin Conjugate Trial Report
No quantitative efficacy data were disclosed; however, a new industry report highlights early Phase 1/2 signals for bicycle toxin...
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 Innovation Clinical Trial Operations Clinical Trial Ops Brief 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 quantitative efficacy data were disclosed; however, a new industry report highlights early Phase 1/2 signals for bicycle toxin...
MediciNova has completed enrollment in its Phase 2b/3 COMBAT-ALS trial of MN-166 (ibudilast) for amyotrophic lateral sclerosis (ALS). The...
Topline: The 2025 ESC/EAS Focused Update assigns Class I, Level A support for non-statin therapies with proven cardiovascular benefit...
AMALFI reported a 6.8% new AFib diagnosis rate with a single 14-day Zio long-term continuous monitoring patch, compared to...
No approved RNA Polymerase I inhibitors are on the market, but the lead asset, pindnarulex (CX-5461), has advanced into...
In early clinical data from a Phase 1 trial in esophageal squamous cell carcinoma, the bispecific antibody drug conjugate...
Gedatolisib delivered a hazard ratio of 0.24 for progression-free survival in the PIK3CA wild-type cohort of the Phase 3...
Telitacicept reduced the 24-hour urine protein-to-creatinine ratio by 55% compared to placebo at 39 weeks (p < 0.0001) in...
In the Phase 3 SERENITY At-Home trial, BXCL501 120 mcg met its primary endpoint of tolerability for self-administered treatment...
In early clinical testing for esophageal squamous cell carcinoma, the bispecific ADC izalontamab brengitecan reported a confirmed objective response...