PF-07321332
Sponsors
Pfizer
Conditions
BioavailabilityCOVID-19Hepatic Impairment
Phase 1
Study to Estimate the Effects of Hepatic Impairment on the Pharmacokinetics (PK) of PF-07321332
CompletedNCT05005312
Start: 2021-08-31End: 2021-12-07Updated: 2023-09-06
Relative Bioavailability Study of 4 Different Formulations of PF-07321332 Relative to the Commercial Tablet Formulation
CompletedNCT05263895
Start: 2022-03-03End: 2022-05-16Updated: 2025-06-11
Phase 2
EPIC-HR: Study of Oral PF-07321332/Ritonavir Compared With Placebo in Nonhospitalized High Risk Adults With COVID-19
CompletedNCT04960202
Start: 2021-07-16End: 2022-04-25Updated: 2025-07-10
Evaluation of Protease Inhibition for COVID-19 in Standard-Risk Patients (EPIC-SR).
TerminatedNCT05011513
Start: 2021-08-25End: 2022-07-25Updated: 2023-08-14
A Study of a Potential Oral Treatment to Prevent COVID-19 in Adults Who Are Exposed to Household Member(s) With a Confirmed Symptomatic COVID-19 Infection
CompletedNCT05047601
Start: 2021-09-09End: 2022-04-12Updated: 2023-05-06