drugset / Trial / NCT07412288

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

NCT07412288 ↗

Phase 1 Recruiting 96 enrolled Kymera Therapeutics, Inc.
RandomizedSequentialDouble-blindOther

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.

Timeline

Start
2026-02-23
Primary completion
2026-12
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator KT-579 Unknown — Oral

Indications

No indication recorded.