A Study Examining the Medication Apremilast as Treatment for Chronic Itch
Part of paid clinical trials in St Louis, Missouri.
- Sponsor
- Washington University School of Medicine
- Study ID
- NCT03239106
- Phase
- PHASE2
- Status
- Completed
Conditions
- Itch
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Apremilast — DRUGApremilast 30 mg BID daily
Study Details
Chronic Itch is a debilitating condition affecting many people. Currently, there are no FDA-approved treatments. Apremilast is an FDA-approved oral medication used to successfully treat the inflammatory skin disorder psoriasis and the inflammatory disorder psoriatic arthritis. This study examines if apremiliast taken twice daily relieves chronic itch.
Key Dates
- First listed
- Aug 3, 2017
- Start date
- Dec 1, 2017
- Status verified
- Jun 2021
- Primary completion
- Oct 31, 2018
- Completion
- Sep 19, 2019
Study Design
- Enrollment
- 10 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: open labelAll participants will receive Apremilast 30 mg BID.
Primary Outcome Measure
Absolute NRS Itch Score at Week 16 (End of Treatment) [ Time Frame: Week 16 ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Washington University Division of Dermatology | St Louis | Missouri | 63108 | - |
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