An Interventional Efficacy and Safety, Phase 3, Double-Blind, 2-Arm Study to Investigate Orally Administered Ibuzatrelvir Compared with Placebo in Non-Hospitalized Symptomatic Adult and Adolescent Participants with COVID-19 Who Are at High Risk of Progressing to Severe Illness

Date Added
June 17th, 2026
PRO Number
Pro00150251
Researcher
John McKinnon

List of Studies

Keywords
COVID-19, Coronavirus
Summary

This is a double‑blind, placebo‑controlled study, meaning participants may receive either the study medication, Ibuzatrelvir, or a placebo. The goal is to see whether the study medication helps participants recover faster and lowers the risk of hospitalization or severe illness. Participant safety is closely monitored.

You can change your mind and stop taking part in the study at any time and for any reason. You will not lose any benefits or care you would normally receive.

If you would like more information about this study, please contact the study team.

Institution
MUSC
Recruitment Contact
Jamila Williams
(843) 792-1088
keithja@musc.edu



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