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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