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Clinical Trial Summary

This study has two parts. Part A will assess the safety, tolerability and pharmacokinetics (PK) of AT-777 in healthy subjects. Part B will assess the safety, antiviral activity/efficacy and PK of AT-777 in combination with AT-527 after 8 weeks of treatment in HCV-infected subjects.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04309734
Study type Interventional
Source Atea Pharmaceuticals, Inc.
Contact
Status Withdrawn
Phase Phase 1/Phase 2
Start date October 2021
Completion date September 2022

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