Study To Assess Efficacy, Safety, Tolerability And Pharmacokinetics Of PF-07038124 Ointment In Participants With Atopic Dermatitis Or Plaque Psoriasis
Completed · Phase 2
Conditions studied: Atopic Dermatitis, Plaque Psoriasis
In brief
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.
Key facts
- Study ID
- NCT04664153
- Run by
- Pfizer
- People needed
- 104
- Starts
- 2020-12-21
- Expected to finish
- 2021-08-18
- Last updated by the study team
- 2022-08-26
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Atopic Dermatitis (AD): Have been diagnosed with AD for at least 3 months; Have an Investigator's Global Assessment (IGA) score of 2 (mild), or 3 (moderate); Have AD covering 5% to 20% (inclusive) of BSA.
- Plaque psoriasis: Have been diagnosed with plaque psoriasis (psoriasis vulgaris) for at least 6 months; Have a Physician Global Assessment (PGA) score of 2 (mild), or 3 (moderate); Having plaque psoriasis covering 5% to 15% (inclusive) of BSA.
You may not qualify if…
- Presence of skin comorbidities that would interfere with study assessment or response to treatment.
- Current or recent history of severe, progressive, or uncontrolled renal, hepatic, hematological, gastrointestinal, metabolic, endocrine, pulmonary, cardiovascular, or neurological disease.
- Other medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior or laboratory abnormality that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study.
Where it is running
- First OC Dermatology — Fountain Valley, California, United States
- Renaissance Research and Medical Group — Cape Coral, Florida, United States
- Olympian Clinical Research — Clearwater, Florida, United States
- Moonshine Research Center, Inc. — Doral, Florida, United States
- Clinical Neuroscience Solutions — Orlando, Florida, United States
- Center for Clinical Studies — Tampa, Florida, United States
- Dawes Fretzin Clinical Research Group, LLC — Indianapolis, Indiana, United States
- The Indiana Clinical Trials Center, PC — Plainfield, Indiana, United States
- Henry Ford Medical Center, New Center One — Detroit, Michigan, United States
- M3 Wake Research, Inc. — Raleigh, North Carolina, United States
- Oregon Dermatology and Research Center — Portland, Oregon, United States
- Clinical Neuroscience Solutions, Inc. dba CNS Healthcare — Memphis, Tennessee, United States
- studies in Dermatology, LLC — Cypress, Texas, United States
- Center for Clinical Studies — Houston, Texas, United States
- Center for Clinical Studies, LTD. LLP — Webster, Texas, United States
- Australian Clinical Research Network — Maroubra, New South Wales, Australia
- Emeritus Research — Camberwell, Victoria, Australia
- Dermatrials Research Inc. — Hamilton, Ontario, Canada
- Lynderm Research Inc. — Markham, Ontario, Canada
- DermEdge Research — Mississauga, Ontario, Canada
- Innovaderm Research Inc. — Montreal, Quebec, Canada
- Centre de Recherche Dermatologique du Quebec metropolitain — Québec, Canada
- NZOZ Specjalistyczny Osrodek Dermatologiczny DERMAL — Bialystok, Poland
- Mazowieckie Centrum Badań Klinicznych — Grodzisk Mazowiecki, Poland
- Centrum Medyczne Angelius Provita — Katowice, Poland
Full record on ClinicalTrials.gov
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