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A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of PF-06842874 in Healthy Participants

2019-10-17 11:03:40 | BioPortfolio

Summary

This study will be the first time PF-06842874 is administered to humans. The purpose of Part A of the study is to investigate the safety, tolerability, and pharmacokinetics of PF-06842874 following administration of single oral doses as an immediate-release formulation to healthy adult participants. Part B of this study will evaluate the relative bioavailability of a modified-release formulation of PF-06842874 for its potential use in future clinical studies. The effect of food on PF-06842874 pharmacokinetics may also be evaluated in this study.

Study Design

Conditions

Healthy Participants

Intervention

PF-06842874, Placebo, Relative Bioavailability

Location

Pfizer New Haven Clinical Research Unit
New Haven
Connecticut
United States
06511

Status

Not yet recruiting

Source

Pfizer

Results (where available)

View Results

Links

Published on BioPortfolio: 2019-10-17T11:03:40-0400

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