Report: Surging Bispecific ADC Trials Eye FDA Approval 2025
In early clinical testing for esophageal squamous cell carcinoma, the bispecific ADC izalontamab brengitecan reported a confirmed objective response...
In early clinical testing for esophageal squamous cell carcinoma, the bispecific ADC izalontamab brengitecan reported a confirmed objective response...
Kyverna outlined a registrational path for KYV-101 in generalized myasthenia gravis (MG), converting its KYSA-6 study into a Phase...
In its pivotal Phase 3 study, arimoclomol (MIPLYFFA) halted disease progression versus placebo over 12 months on the NPC...
No new efficacy or safety numbers were disclosed. Still, AAVantgarde Bio will present updated Phase 1/2 LUCE-1 data for...
Anavex Life Sciences has published preclinical data in •iScience• further elucidating the mechanism by which its SIGMAR1 (S1R) agonist,...
Incannex Healthcare’s Phase 2 trial of PSX-001 (formerly Psi-GAD), a psilocybin-assisted therapy for generalized anxiety disorder (GAD), demonstrated statistically...
Marker Therapeutics’ Phase 1 APOLLO study of MT-601 in relapsed B-cell lymphoma patients yielded a 66% objective response rate...
Cemdisiran monotherapy, administered subcutaneously every three months, demonstrated a 2.3-point placebo-adjusted improvement in the Myasthenia Gravis Activities of Daily...
BioXcel Therapeutics’ BXCL501, a sublingual dexmedetomidine film, met its primary endpoint of tolerability in the SERENITY At-Home Phase 3...
In Stage A of a Phase 3 trial in China, RemeGen’s telitacicept achieved a 55% reduction in 24-hour urine...