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A Study to Evaluate Mavacamten in Adolescents With Symptomatic Obstructive Hypertrophic Cardiomyopathy
NCT06253221 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the efficacy, safety, and pharmacokinetics of mavacamten in adolescent patients with symptomatic obstructive hypertrophic cardiomyopathy (HCM).
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Mavacamten
Study Locations (20)
California
- Local Institution - 0032 — Los Angeles
- Local Institution - 0008 — Los Angeles
- Local Institution - 0033 — Palo Alto
- Local Institution - 0044 — San Diego
New York
- Local Institution - 0010 — New Hyde Park
- Local Institution - 0024 — New York
- Local Institution - 0036 — New York
- Local Institution - 0040 — The Bronx
Alabama
- Local Institution - 0017 — Birmingham
Arizona
- Local Institution - 0050 — Phoenix
Colorado
- Local Institution - 0038 — Aurora
Florida
- Local Institution - 0031 — St. Petersburg
Georgia
- Local Institution - 0053 — Atlanta
Illinois
- Local Institution - 0013 — Chicago
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 44 participants |
| Start Date | 2024-04-17 |
| Est. Completion | 2031-03-28 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06253221
The ClinicalTrials.gov registry entry for NCT06253221 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 44 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 504 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Cardiomyopathy, Hypertrophic appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06253221 reports 20 study locations spanning 14 distinct geographic areas — top geographies include California, New York, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06253221 about?
NCT06253221 is a clinical study titled "A Study to Evaluate Mavacamten in Adolescents With Symptomatic Obstructive Hypertrophic Cardiomyopathy". The purpose of this study is to evaluate the efficacy, safety, and pharmacokinetics of mavacamten in adolescent patients with symptomatic obstructive hypertrophic cardiomyopathy (HCM).
What is the current status of trial NCT06253221?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 44 participants. The study started on 2024-04-17. Estimated completion is 2031-03-28.
What conditions does trial NCT06253221 study?
This clinical trial studies the following conditions: Cardiomyopathy, Hypertrophic. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06253221?
The interventions under investigation include: Placebo (DRUG), Mavacamten (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06253221?
This trial is sponsored by Bristol-Myers Squibb, which has 504 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06253221 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Colorado, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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