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Not Yet RecruitingNCT07456059

A Study to Evaluate EDG-7500 in Caucasian and Japanese Adults

A Phase 1, Single-center, Open-label, Study to Investigate the Safety, Tolerability, and Pharmacokinetics of a Single Dose and Multiple Doses of EDG-7500 in Healthy Adult Caucasian and Japanese Participants

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
24 (estimated)
Sponsor
Edgewise Therapeutics, Inc. · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The purpose of this Phase 1 study is to understand and compare the amount of EDG-7500 in the blood after single and multiple doses in Japanese and Caucasian adults. The safety of EDG-7500 in these adult participants will also be evaluated in this study.

Conditions

Interventions

TypeNameDescription
DRUGEDG-7500Solid oral formulation of EDG-7500

Timeline

Start date
2026-03-01
Primary completion
2026-06-01
Completion
2026-06-01
First posted
2026-03-06
Last updated
2026-03-06

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07456059. Inclusion in this directory is not an endorsement.

A Study to Evaluate EDG-7500 in Caucasian and Japanese Adults (NCT07456059) · Clinical Trials Directory