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Clinical Trial Summary

This study will assess the PK and rates of elimination and mass balance of total radioactivity from [14C]-PC14586


Clinical Trial Description

PC14586 is a first-in-class, oral, small molecule p53 reactivator that is selective for the TP53 Y220C mutation. The study will assess the PK, absorption, metabolism, and excretion of [14C]-PC14586 following a single dose in healthy male participants. The aim is to recruit approximately 8 participants with a minimum number of 6 evaluable participants. Each participant will be admitted to the study site pre-dose on Day -1 and will remain at the study site until at least Day 14. Participants will receive a single administration of [14C]-PC14586 as oral capsules on Day 1. During this study, whole blood, plasma, urine, feces, and vomit samples (if presented) will be collected at various timepoints to characterize the absorption, metabolism, excretion, and PK of [14C]-PC14586. The duration of the residential period will be evaluated following the administration of [14C]-PC14586 and may be extended to ensure recovery of at least 90% of the total radioactivity, or until less than 1% of dose is recovered in urine and/or feces. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05523687
Study type Interventional
Source PMV Pharmaceuticals, Inc
Contact
Status Completed
Phase Phase 1
Start date September 6, 2022
Completion date November 30, 2022

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