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Clinical Trial Summary

The purpose of the study is to evaluate the safety, (local and systemic) tolerability, and pharmacokinetics following multiple doses of topically applied, maximum feasible formulations of PF-07295324 (0.12% w/w) or PF-07259955 (2% w/w), on approximately 20% body surface area (BSA), in healthy adult participants.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05206604
Study type Interventional
Source Pfizer
Contact
Status Completed
Phase Phase 1
Start date February 9, 2022
Completion date August 12, 2022

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