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Trial · NCT07557498

Registered outcomes24

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

ListOutcomeTime frameDescription
PrimaryTime to mavacamten treatment resumptionBaseline, and at weeks 4, 8, 12, 24Group 1 only
PrimaryType of hypertrophic cardiomyopathy (HCM) background therapy prescribedBaseline, and at weeks 4, 8, 12, 24Group 1 only
PrimaryType of changes to hypertrophic cardiomyopathy (HCM) background therapyAt baseline, weeks 4, 8, 12, 24Group 1 only. Type of changes include initiation, switching, discontinuation, augmentation, dose titration
SecondaryPerspectives on treatment preference, and the eligibility, onboarding and implementation of mavacamten as assessed by feedback collated through structured physician interviewsUp to week 24Group 2 only

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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