drugset / Trial / NCT05206604

A First-in-human Study of Multiple Doses of Topically Administered PF-07295324 and PF-07259955

NCT05206604 ↗

Phase 1 Completed 24 enrolled Pfizer
RandomizedSequentialTriple-blindTreatment

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.

Timeline

Start
2022-02-09
Primary completion
2022-08-12
Completion
2022-08-12

Drugs

EvaluationDrugModalityDoseRoute
Subject PF-07259955 Unknown 2 % Topical
Subject PF-07295324 Unknown 0.12 % Topical

Indications

No indication recorded.