The Study of Bemnifosbuvir in Healthy Japanese Subjects
Completed · Phase 1
Conditions studied: Healthy Volunteer Study
In brief
This study will assess the safety, tolerability and pharmacokinetics (PK) of Bemnifosbuvir in healthy adult Japanese subjects
Key facts
- Study ID
- NCT05905497
- Run by
- Atea Pharmaceuticals, Inc.
- People needed
- 14
- Starts
- 2023-04-26
- Expected to finish
- 2023-05-19
- Last updated by the study team
- 2023-06-15
Who can join
Age: 18 and older, up to 64. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Must agree to use two methods of birth control from Screening through 90 days after administration of the last dose of study drug
- Females must have a negative pregnancy test at Screening and prior to dosing
- Minimum body weight of 50 kg and body mass index (BMI) of 18-32 kg/m2
- Willing to comply with the study requirements and to provide written informed consent
- The subject must have been born in Japan and have both parents and 4 grandparents of Japanese descent
- The subject must have lived outside of Japan for no more than 10 years
You may not qualify if…
- Pregnant or breastfeeding
- Infected with hepatitis B virus, hepatitis C virus, HIV or COVID-19
- Abuse of alcohol or drugs
- Use of other investigational drugs within 28 days of dosing
- Other clinically significant medical conditions or laboratory abnormalities
Where it is running
- Atea Study Site — Cypress, California, United States
Full record on ClinicalTrials.gov
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