Atsena’s ATSN-201 and ATSN-101 Show Sustained Efficacy in Gene Therapy Trials
Atsena's ATSN-201 and ATSN-101 show sustained efficacy in gene therapy trials with zero serious adverse events through 36 months.
Atsena's ATSN-201 and ATSN-101 show sustained efficacy in gene therapy trials with zero serious adverse events through 36 months.
Artiva's AlloNK achieves 54% ACR50 response in refractory rheumatoid arthritis patients, outpacing rituximab alone in early trial data.
Celldex completes barzolvolimab Phase 3 enrollment of 1,939 patients across two trials, advancing topline data to Q4 2026.
FDA approves efgartigimod for all adult myasthenia gravis types, including seronegative patients previously excluded from treatment options.
4DMT completes 4FRONT-1 randomization of all 523 participants with topline data expected in H1 2027, backed by $458M cash...
Atsena's ATSN-201 and ATSN-101 gene therapies demonstrate sustained structural and functional improvements at 12 and 36 months in Phase...
RAP-219's revised 22-day half-life extends seizure control weeks past treatment and reshapes Phase 3 design for focal onset seizures.
Celldex's Phase 3 CSU Trial enrolls 1,939 patients six months ahead of schedule, representing the largest randomized trial in...
Denali pursues DNL593 progranulin replacement in FTD-GRN after Takeda exit, with Phase 1/2 data expected by year-end in a...
Praxis reported 77% placebo-adjusted seizure reduction in SCN2A epilepsy, with all treated patients showing improvements in sleep, motor function,...