Clinical Trial

First-in-human Study of Orally Administered KT-579 in Healthy Adult Participants

Recruiting Phase 1
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Summary
This is a first-in-human study to evaluate safety and tolerability, pharmacokinetics, and pharmacodynamics of single and multiple dose levels of KT-579 in healthy male and female adult participants.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-02-09.
Trial Details
NCT Number NCT07412288
Lead Sponsor Kymera Therapeutics, Inc.
Conditions Healthy Participants
Enrollment 96 participants
Start Date 2026-02-23
Primary Completion 2026-12 (estimated)
Study Completion 2026-12 (estimated)
Updated on ClinicalTrials.gov 2026-02-27