Satellos Advances Duchenne Pill Trial in Children; Idorsia Raises $81 Million

Satellos; Duchenne muscular dystrophy; SAT-3247; Phase 2 clinical trial; children; FDA IND submission; oral small-molecule therapy; Idorsia; fundraising; biotech

Rallybio Halts Development of Lead FNAIT Program Following Phase 2 Failure

Rallybio RLYB212, Fetal and neonatal alloimmune thrombocytopenia (FNAIT), Phase 2 clinical trial, Maternal immune disorder therapy, Biotech pipeline shift