Bristol Myers Squibb stock extends Camzyos evidence in adolescents
Published on 11/09/2026 at 16:26 | Editorial responsibility: Rafael Müller, Editor-in-Chief AD HOC NEWSCamzyos evidence expands in adolescents
- The Phase 3 SCOUT-HCM trial followed 44 adolescents with symptomatic obstructive hypertrophic cardiomyopathy through 56 weeks.
- Continuous Camzyos treatment produced a mean 48.1 mmHg reduction in the Valsalva left ventricular outflow tract gradient.
- Further cardiovascular data were scheduled for presentation at the American Heart Association Scientific Sessions through November 9.
Bristol Myers Squibb presented 56-week results from the Phase 3 SCOUT-HCM trial on Friday, November 6, at the Hypertrophic Cardiomyopathy Medical Society Scientific Sessions in Chicago. The company said the data extend evidence for Camzyos in adolescents with symptomatic obstructive hypertrophic cardiomyopathy.
The stock later traded at 55.50 euros on Lang & Schwarz at 16:13 CET on Monday, November 9, 2026. That quote was 1.58 percent below the 56.39 euros cited in the earlier report at 12:42 CET the same day, a separate comparison from the Xetra daily close.
What changed for Camzyos
SCOUT-HCM randomized 44 patients aged 12 to under 18, with 43 completing the initial 28-week placebo-controlled period and continuing into active treatment. Patients who received mavacamten throughout the study recorded a mean change from baseline of minus 48.1 mmHg in the Valsalva left ventricular outflow tract gradient after 56 weeks.
Patients who switched from placebo to Camzyos at week 28 achieved a similar reduction. The trial also reported meaningful improvements in several secondary endpoints, according to the Bristol Myers Squibb investor release.
Why it matters for investors
No patient experienced a left ventricular ejection fraction below 50 percent during the 56-week evaluation. The continuous-treatment group recorded five treatment-related adverse events and two serious events, while the crossover group recorded one treatment-related event and no serious event during its active-treatment period.
The U.S. Food and Drug Administration approved Camzyos for pediatric patients weighing at least 30 kilograms in September 2026. The expanded follow-up strengthens the evidence base for a newly eligible patient segment, although the small trial population and continuing safety monitoring remain relevant to expectations for uptake.
The company planned additional Camzyos presentations covering clinical and real-world evidence at the American Heart Association Scientific Sessions through Monday, November 9.
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Bristol Myers Squibb stock facts
- Company: Bristol Myers Squibb
- ISIN: US1101221083
- Ticker: BMY
- Home exchange: New York Stock Exchange
- Lang & Schwarz quote: 55.50 euros at 16:13 CET on November 9, 2026
