
Probably the most important news this month is the press release published by Bristol Myers Squibb, the manufacturer of mavacamten, regarding the negative results of the Phase 3 ODYSSEY-HCM trial evaluating the drug in patients with symptomatic non-obstructive hypertrophic cardiomyopathy (nHCM). The study did not meet its dual primary endpoints—improvement in symptoms (KCCQ-23 CSS) and peak oxygen consumption (pVO2) after 48 weeks. Experts emphasized that the results highlight the differences between obstructive and non-obstructive HCM and underscore the need for new treatment approaches for nHCM


