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Completed Phase 2 Interventional Results available

Study To Assess Efficacy, Safety, Tolerability And Pharmacokinetics Of PF-07038124 Ointment In Participants With Atopic Dermatitis Or Plaque Psoriasis

ClinicalTrials.gov ID: NCT04664153

Public ClinicalTrials.gov record NCT04664153. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 12:14 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A PHASE 2A, RANDOMIZED, DOUBLE BLIND, VEHICLE CONTROLLED, PARALLEL GROUP STUDY TO ASSESS THE EFFICACY, SAFETY, TOLERABILITY AND PHARMACOKINETICS OF PF-07038124 OINTMENT FOR 6 WEEKS IN PARTICIPANTS WITH MILD TO MODERATE ATOPIC DERMATITIS OR PLAQUE PSORIASIS

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is being conducted to provide data on efficacy, safety, tolerability and PK of PF-07038124 ointment versus vehicle control in the treatment of mild to moderate AD and mild to moderate plaque psoriasis.

Study identification

NCT ID
NCT04664153
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
104 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 21, 2020 (Actual)
Primary completion
Aug 18, 2021 (Actual)
Completion
Aug 18, 2021 (Actual)
Last update posted
Aug 26, 2022

2020 – 2021

United States locations

U.S. sites
15
U.S. states
8
U.S. cities
15
Facility City State ZIP Site status
First OC Dermatology Fountain Valley California 92708 —
Renaissance Research and Medical Group Cape Coral Florida 33991 —
Olympian Clinical Research Clearwater Florida 33756 —
Moonshine Research Center, Inc. Doral Florida 33166 —
Clinical Neuroscience Solutions Orlando Florida 32801 —
Center for Clinical Studies Tampa Florida 33613 —
Dawes Fretzin Clinical Research Group, LLC Indianapolis Indiana 46250 —
The Indiana Clinical Trials Center, PC Plainfield Indiana 46168 —
Henry Ford Medical Center, New Center One Detroit Michigan 48202 —
M3 Wake Research, Inc. Raleigh North Carolina 27612 —
Oregon Dermatology and Research Center Portland Oregon 97210 —
Clinical Neuroscience Solutions, Inc. dba CNS Healthcare Memphis Tennessee 38119 —
studies in Dermatology, LLC Cypress Texas 77433 —
Center for Clinical Studies Houston Texas 77004 —
Center for Clinical Studies, LTD. LLP Webster Texas 77598 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04664153, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 26, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04664153 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →