A Study of Escalating Doses of Itacitinib Administered Orally in Patients With Plaque Psoriasis
Completed · Phase 2 · Has a placebo group
Conditions studied: Plaque Psoriasis
In brief
This is a study of itacitinib in patients with chronic plaque psoriasis. This study will evaluate safety and efficacy parameters of itacitinib.
Key facts
- Study ID
- NCT01634087
- Run by
- Incyte Corporation
- People needed
- 50
- Starts
- 2012-06-01
- Expected to finish
- 2013-02-01
- Last updated by the study team
- 2019-03-12
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects with chronic plaque psoriasis aged 18 to 75 who have had insufficient response to topical agents, and who meet the psoriasis assessment expectations as defined in the study protocol
You may not qualify if…
- Females who are pregnant or breastfeeding
- Men and women who cannot comply with requirements to avoid fathering a child or becoming pregnant, respectively
- Subjects treated with leflunomide or other biological therapies to treat psoriasis and all JAK-STAT inhibitors within 12 weeks prior to first dose of study drug
Where it is running
- Study site — Hot Springs, Arkansas, United States
- Study site — Los Angeles, California, United States
- Study site — Clinton, Minnesota, United States
- Study site — Fridley, Minnesota, United States
- Study site — Rochester, New York, United States
- Study site — Moncton, New Brunswick, Canada
- Study site — Windsor, Ontario, Canada
- Study site — Montreal, Quebec, Canada
- Study site — Québec, Canada
Full record on ClinicalTrials.gov
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