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Study of AT-587 in Healthy Subjects

Study of AT-587 in Healthy Subjects

Recruiting
18-65 years
All
Phase 1
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  • Simplified (AI rewritten)

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Overview

This study will assess the safety, tolerability and pharmacokinetics (PK) of AT-587 in healthy subjects

Description

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

Eligibility

Inclusion Criteria:

  • Body mass index (BMI) of 18-29 kg/m2
  • Must agree to use protocol-specified methods of contraception
  • Negative pregnancy test
  • Willing to comply with the study requirements and to provide written informed consent

Exclusion Criteria:

  • Pregnant or breastfeeding
  • Abuse of alcohol or drugs
  • Use of other investigational drugs within 30 days of dosing
  • Other clinically significant medical conditions

Study details
    Hepatitis E

NCT07728487

Atea Pharmaceuticals, Inc.

1 August 2026

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A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

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