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Active Not RecruitingNCT06347159

A Study of EDG-7500 in Adults With Hypertrophic Cardiomyopathy (CIRRUS-HCM)

An Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of EDG-7500 in Adults With Hypertrophic Cardiomyopathy

Status
Active Not Recruiting
Phase
Phase 2
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Edgewise Therapeutics, Inc. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is being conducted in order to understand the safety and effects of different doses of EDG-7500 as a single dose in adults with obstructive hypertrophic cardiomyopathy (oHCM) and as multiple doses in adults with obstructive or nonobstructive hypertrophic cardiomyopathy (nHCM).

Conditions

Interventions

TypeNameDescription
DRUGEDG-7500Liquid suspension formulation of EDG-7500
DRUGEDG-7500Solid oral formulation of EDG-7500

Timeline

Start date
2024-04-11
Primary completion
2026-06-01
Completion
2026-12-01
First posted
2024-04-04
Last updated
2026-02-27

Locations

21 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT06347159. Inclusion in this directory is not an endorsement.

A Study of EDG-7500 in Adults With Hypertrophic Cardiomyopathy (CIRRUS-HCM) (NCT06347159) · Clinical Trials Directory