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A Phase 1 Relative Bioavailability Study of 4 Different Formulations of PF-07321332 Compared to the Commercial Tablet Formulation in Healthy Participants

A Phase 1 Relative Bioavailability Study of 4 Different Formulations of PF-07321332 Compared to the Commercial Tablet Formulation in Healthy Participants. A Phase 1, Open-Label, Randomized, Single-Dose, Crossover Study to Estimate the Relative Bioavailability of PF-07321332 Following Oral Administration of 4 Different Formulations Relative to the Commercial Tablet Formulation in Healthy Adult Participants Under Fasted Conditions.

Category & Conditions: Coronavirus Disease (COVID-19)
Medicine: PAXLOVID
ClinicalTrials.gov Identifier (NCT): NCT05263895
Protocol ID: C4671008
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