Study of AT-587 in Healthy Subjects
A Phase 1, First-in-Human (FIH), Single-center, Randomized, Double-blind, Placebo-controlled, Single and Multiple Ascending Dose Trial to Evaluate the Safety, Tolerability, and Pharmacokinetics (PK) of AT-587 in Healthy Adult Participants
Atea Pharmaceuticals, Inc.
62 participants
Jul 13, 2026
INTERVENTIONAL
Conditions
Summary
This study will assess the safety, tolerability and pharmacokinetics (PK) of AT-587 in healthy subjects
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
Parallel Assignment
Parallel Assignment
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07728487