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NCT05719805 · ClinicalTrials.gov registry record · Phase 1

A Study to Evaluate the Effects of Mavacamten in Healthy Participants

A Phase 1 study of Healthy Participants, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
84
Enrollment target
2
Study locations

NCT05719805: Completed Phase 1 study of Healthy Participants, sponsored by Bristol-Myers Squibb.

NCT05719805 is a Phase 1 study of Healthy Participants that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 84 participants, above the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (29% higher). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05719805, a Phase 1 study of Healthy Participants, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
84 participants
Enrollment target
2
Study locations

Study Summary

The purpose of the study is to evaluate the effect between two different single doses of mavamten in healthy participants.

Conditions Studied

Interventions

  • DRUG Mavacamten

Study Locations (2)

Florida

  • Local Institution - 0001 - Miami

Minnesota

  • Local Institution - 0002 - Saint Paul

Trial Details

FieldValue
Enrollment Target 84 participants
Start Date 2023-02-20
Est. Completion 2023-07-25
Phase Phase 1
Bristol-Myers Squibb

1,025 total trials

What the finished NCT05719805 record still lists

NCT05719805 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 84 participants, a relatively small participant target, above the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (29% higher).

The record links to 1 condition, with Healthy Participants appearing as the primary indexed condition, and to 1 intervention - of which Mavacamten is the first listed.

NCT05719805 reports a single indexed study location in Florida, Minnesota.

Frequently Asked Questions

What is clinical trial NCT05719805 about?

NCT05719805 is a clinical study titled "A Study to Evaluate the Effects of Mavacamten in Healthy Participants". The purpose of the study is to evaluate the effect between two different single doses of mavamten in healthy participants.

What is the current status of trial NCT05719805?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 84 participants. The study started on 2023-02-20. Estimated completion is 2023-07-25.

What conditions does trial NCT05719805 study?

This clinical trial studies the following conditions: Healthy Participants.

What interventions are being tested in trial NCT05719805?

The interventions under investigation include: Mavacamten (DRUG).

Who is sponsoring clinical trial NCT05719805?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05719805 being conducted?

This trial has 2 study locations across Florida, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Healthy Participants

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05719805's enrollment target sits among peer trials

84 30th of 119 higher than 89 of 119 other Healthy Participants trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Healthy Participants trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05719805, the US trial registry maintained by the National Library of Medicine. NCT05719805 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.