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Trial · NCT07107373

Registered outcomes11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryNew York Heart Association (NYHA) functional classBaseline, and at weeks 4, 8, 12, 24, 36, 48, 60, 72, and in increments of 12 weeks thereafter from index
PrimaryLeft ventricular outflow tract (LVOT) gradient and associated parametersBaseline, and at weeks 4, 8, 12, 24, 36, 48, 60, 72, and in increments of 12 weeks thereafter from index
PrimaryLeft ventricular ejection fraction (LVEF) and associated parametersBaseline, and at weeks 4, 8, 12, 24, 36, 48, 60, 72, and in increments of 12 weeks thereafter from index
SecondaryMavacamten dose at initiationDay 1
SecondaryMavacamten dose changeUp to 72 weeks
SecondaryReason for mavacamten dose changeUp to 72 weeks
SecondaryReason for mavacamten permanent discontinuationUp to 72 weeks
SecondaryReason for treatment interruptionUp to 72 weeks
SecondaryPrior Obstructive hypertrophic cardiomyopathy (oHCM) therapiesBaseline
SecondaryConcurrent Obstructive hypertrophic cardiomyopathy (oHCM) therapiesUp to 72 weeks
SecondaryOther cardiovascular-related treatments prescribedUp to 72 weeks

Source ClinicalTrials.govtrials-2026-11-12-0.4.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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