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RECRUITING
NCT07728487
PHASE1
Study of AT-587 in Healthy Subjects
Sponsor: Atea Pharmaceuticals, Inc.
View on ClinicalTrials.gov
Summary
This study will assess the safety, tolerability and pharmacokinetics (PK) of AT-587 in healthy subjects
Official title: 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
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
62
Start Date
2026-07-13
Completion Date
2026-12
Last Updated
2026-07-27
Healthy Volunteers
Yes
Conditions
Interventions
DRUG
AT-587
Parallel Assignment
OTHER
Placebo
Parallel Assignment
Locations (1)
Atea Study Site
Edegem, Belgium