Trial Search Results

A Study to Evaluate Mavacamten in Adults With Symptomatic Obstructive HCM Who Are Eligible for Septal Reduction Therapy

This is a randomized, double-blind, placebo-controlled, multi-center study in the United States (U.S.) that will evaluate the effect of mavacamten treatment on reducing the number of septal reduction therapy (SRT) procedures performed in subjects with symptomatic obstructive hypertrophic cardiomyopathy (oHCM [also known as HOCM]) who are eligible for SRT based on ACCF/AHA 2011 and/or ESC 2014 guidelines.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Bristol-Myers Squibb

Stanford Investigator(s):

Intervention(s):

  • Drug: Mavacamten
  • Drug: Placebo

Phase:

Phase 3

Eligibility


Key Inclusion Criteria:

   - At least 18 years old at screening and body weight > 45 kg at screening

   - Diagnosed with oHCM consistent with current ACCF/AHA 2011 and/or ESC 2014 guidelines
   and meet their recommendations for invasive therapies

   - Referred or under active consideration within the past 12 months for SRT procedure and
   willing to have SRT procedure

   - Has documented left ventricular ejection fraction (LVEF) ≥ 60% at Screening

   - Has documented oxygen saturation at rest ≥ 90% at Screening

Key Exclusion Criteria:

   - Persistent or permanent atrial fibrillation and subject not on anticoagulation for ≥ 4
   weeks prior to screening and/or not adequately rate controlled ≤ 6 months prior to
   screening

   - Previously treated with invasive septal reduction (surgical myectomy or percutaneous
   alcohol septal ablation [ASA])

   - For individuals on beta blockers, calcium channel blockers, or disopyramide, any dose
   adjustment of these medications < 14 days prior to screening or an anticipated change
   in regimen during the first 16 weeks of the study

   - Any medical condition that precludes upright exercise stress testing

   - Paroxysmal, intermittent atrial fibrillation with atrial fibrillation present at
   screening

   - Prior treatment with cardiotoxic agents, such as doxorubicin or similar

   - Has a history or evidence of any other clinically significant disorder, condition, or
   disease that would pose a risk to subject safety or interfere with the study
   evaluation, procedures, or completion

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Nicole Howard
6507256911
Not Recruiting