Study To Evaluate Safety And Efficacy Of PF-06700841 In Subjects With Moderate To Severe Plaque Psoriasis
Completed · Phase 2 · Has a placebo group
Conditions studied: Chronic Plaque Psoriasis
In brief
The purpose of this study is to determine whether PF-06700841 is safe and effective in the treatment of chronic plaque psoriasis.
Key facts
- Study ID
- NCT02969018
- Run by
- Pfizer
- People needed
- 212
- Starts
- 2016-12-01
- Expected to finish
- 2018-03-01
- Last updated by the study team
- 2019-03-29
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Have had a diagnosis of plaque psoriasis (psoriasis vulgaris) for at least 6 months prior to Baseline/Day 1 (prior to first dose of study drug)
- Have a PASI score of 12 or greater AND a PGA score of 3 ("moderate") or 4 ("severe") at Baseline/Day 1 (prior to first dose of study drug)
- Have plaque-type psoriasis covering at least 10% of total body surface area (BSA) at Baseline/Day 1 (prior to first dose of study drug)
- Considered by dermatologist investigator to be a candidate for systemic therapy or phototherapy of psoriasis (either naïve or history of previous treatment)
You may not qualify if…
- Currently have non-plaque forms of psoriasis, eg, erythrodermic, guttate, or pustular psoriasis, with the exception of nail psoriasis which is allowed
- Have evidence of skin conditions (eg, eczema) at the time of screening or baseline visit that would interfere with the evaluation of psoriasis
- Cannot discontinue systemic therapies and/or topical therapies for the treatment of psoriasis and cannot discontinue phototherapy (UVB or PUVA)
- Have previously been treated with Secukinumab (Cosentyx), and Ixekizumab (Taltz).
- Have taken Apremilast (Otezla) within 3 months of first dose of study drug.
- Have undergone treatment with tofacitinib within 3 months of first dose.
Where it is running
- Northwest Arkansas Clinical Trials Center, PLLC/Hull Dermatology, PA — Rogers, Arkansas, United States
- Anaheim Clinical Trials, LLC — Anaheim, California, United States
- California Dermatology & Clinical Research Institute — Encinitas, California, United States
- Emil A. Tanghetti, MD dba Center for Dermatology and Laser Surgery — Sacramento, California, United States
- Southern California Dermatology — Santa Ana, California, United States
- Tower Saint John's Imaging — Santa Monica, California, United States
- Clinical Science Institute — Santa Monica, California, United States
- Park Avenue Dermatology Administrative Annex — Orange Park, Florida, United States
- Park Avenue Dermatology — Orange Park, Florida, United States
- Olympian Clinical Research — Tampa, Florida, United States
- Rose Radiology — Tampa, Florida, United States
- Forward Clinical Trials, Inc — Tampa, Florida, United States
- Dundee Dermatology — West Dundee, Illinois, United States
- Dawes Fretzin Clinical Research Group, LLC — Indianapolis, Indiana, United States
- Dawes Fretzin Dermatology Group, LLC — Indianapolis, Indiana, United States
- Psoriasis Treatment Center of Central New Jersey — East Windsor, New Jersey, United States
- The Rockefeller University — New York, New York, United States
- Skin Search of Rochester, Inc. — Rochester, New York, United States
- Investigational Drug Services, UNC Hospitals — Chapel Hill, North Carolina, United States
- UNC Dermatology and Skin Cancer Center — Chapel Hill, North Carolina, United States
- UNC Clinical and Translation Research Center — Chapel Hill, North Carolina, United States
- Lynn Health Science Institute — Oklahoma City, Oklahoma, United States
- Vital Prospects Clinical Research Institute, P.C — Tulsa, Oklahoma, United States
- Health Concepts — Rapid City, South Dakota, United States
- Center for Clinical Studies — Houston, Texas, United States
Full record on ClinicalTrials.gov
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