- Bristol Myers Squibb reported positive Phase 3 SCOUT-HCM results for Camzyos (mavacamten) in adolescents with symptomatic obstructive hypertrophic cardiomyopathy.
- Trial met primary endpoint, showing least-squares mean Valsalva LVOT gradient reduction versus placebo at Week 28 of 48 mm Hg (P < 0.0001).
- Data were presented as a late-breaking presentation at ACC Annual Scientific Session & Expo 2026, with simultaneous publication in New England Journal of Medicine.
- Safety profile in adolescents matched adult experience, with no new safety signals reported over 28 weeks.
- Study enrolled 44 patients ages 12 to <18, positioning Camzyos as potential first targeted pharmacologic therapy for adolescent oHCM if regulators expand labeling.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Bristol-Myers Squibb Company published the original content used to generate this news brief via Business Wire (Ref. ID: 202603291145BIZWIRE_USPR_____20260327_BW682053) on March 29, 2026, and is solely responsible for the information contained therein.
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