A Study to Understand How the Study Medicine (PF-07081532) is Processed and Eliminated in Healthy Men

PHASE1CompletedINTERVENTIONAL
Enrollment

6

Participants

Timeline

Start Date

December 21, 2022

Primary Completion Date

March 15, 2023

Study Completion Date

March 15, 2023

Conditions
Healthy Participants
Interventions
DRUG

Oral [14C]PF-07081532

A single oral dose of \[14C\]PF-07081532, will be administered as a liquid formulation in study period 1.

DRUG

Oral PF-07081532 and IV [14C]PF-07081532

In study period 2: a single, oral, unlabeled dose of PF-07081532 will be administered as a liquid formulation. Approximately 1 hours after the administration of the unlabeled oral dose, a single dose of \[14C\]PF-07081532 will be administered via intravenous infusion.

Trial Locations (1)

9728 NZ

PRA Health Sciences, Groningen

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY