Arrowhead reported Phase 3 plozasiran results showing robust triglyceride reductions and fewer pancreatitis events, prompting an FDA supplemental NDA submission planned for by end-2026. The data support a favorable safety profile and potential multi-region approvals under the Redemplo brand, driving near-term upside and longer-term regulatory milestones.
ARWR shares rise 17.81% following ARO-INHBE, ARO-ALK7 trial results. Significant reduction in visceral and liver fat reported for ARO-INHBE. ARO-ALK7 shows promising gene target silencing in obesity treatment. Studies are ongoing with further results expected in 2026. Combination with tirzepatide enhances effects of ARO-INHBE significantly.
FDA approved Arrowhead's drug for a genetic disorder causing extremely high blood triglycerides. Approval establishes commercial pathway and materially de-risks Arrowhead's lead program, boosting revenue potential.
Cramer expressed uncertainty about Arrowhead's financial viability. Arrowhead initiated Phase 1/2a study of ARO-ALK7 for obesity treatment. Cramer highlighted strong performance of Dover Corporation's recent earnings. Arrowhead's shares gained 1.3% to settle at $16.61 on Tuesday.
Arrowhead's Plozasiran met primary and key secondary endpoints in Phase 3 trial. No approved treatment exists for familial chylomicronemia syndrome (FCS). Arrowhead plans FDA application for Plozasiran this year. Shares rose 2% amid positive trial news but are down over 20% this year.
Arrowhead's Plozasiran met all primary and key secondary endpoints. FDA application for Plozasiran expected by year's end. Shares rose 2% post-announcement but down over 20% YTD. Plozasiran targets familial chylomicronemia syndrome, a currently untreatable condition. Company views Plozasiran as potentially best-in-class treatment.