A Study to Evaluate Different Oral Formulations of KT-621
A Phase 1, Open-Label, Crossover Study to Evaluate the Relative Bioavailability of Different Oral Formulations of KT-621 in Healthy Adult Participants
Kymera Therapeutics, Inc.
54 participants
Oct 1, 2026
INTERVENTIONAL
Conditions
Summary
This is a Phase I study to evaluate the relative bioavailability and safety and tolerability of different oral formulations of KT-621 in healthy adult participants.
Eligibility
Plain Language Summary
Simplified for easier understanding
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Interventions
KT-621 Reference Oral Formulation
KT-621 Test Oral Formulation #1
KT-621 Test Oral Formulation #2
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07823205