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A Randomized, Double-Blind, Placebo-Controlled Pilot Study to Evaluate the Efficacy, Safety, and Tolerability of AXA1125 in Subjects With Fatigue-Predominant Post-Acute Sequelae of SARS-CoV-2 (PASC) Infection
This study will compare the effects of AXA1125, an orally active mixture of amino acids, compared to placebo, on improving muscle function (metabolism) following moderate exercise in subjects with fatigue-Predominant Post-Acute Sequelae of SARS-CoV-2 as well as the safety and tolerability of AXA1125. Subjects will take one dose of AXA1125 or a placebo twice daily for 28 days.
Age
18 - 64 years
Sex
ALL
Healthy Volunteers
No
Oxford University Hospitals NHS Foundation Trust
Oxford, United Kingdom
Start Date
December 15, 2021
Primary Completion Date
June 21, 2022
Completion Date
June 29, 2022
Last Updated
October 20, 2022
41
ACTUAL participants
AXA1125
DRUG
Placebo
DRUG
Lead Sponsor
Axcella Health, Inc
Data Source & Attribution
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