Utilization of a Microdevice for Psoriasis and Atopic Dermatitis
Part of paid clinical trials in San Francisco, California.
- Sponsor
- University of California, San Francisco
- Study ID
- NCT07352566
- Phase
- PHASE4
- Status
- Not Yet Recruiting
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Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- In situ cutaneous microdevice — DEVICEThe small device, about the size of a grain of rice, has up to 20 tiny reservoirs that hold medications that are approved by the Food and Drug Administration (FDA) for atopic dermatitis and psoriasis. In this study, the device will be tested to see if it's safe and works well for predicting how the skin will react to standard treatments. The microdevice will contain a subset of the following: Triamcinolone, 5-fluorouracil, Calcipotriene, Tapinarof, Crisaborole, Tacrolimus, Adalimumab, Etanercept, Certolizumab, Infliximab, Secukinumab, Ixekizumab, Apremilast, Risankizumab, Ustekinumab, Hydroxychloroquine, Methotrexate, Mycophenolate, Azathioprine, Chloroquine, Cyclosporine, Tofacitinib, Deucravacitinib, Dupilumab, Tralokinumab, Guselkumab, Tildrakizumab, Baractinib, Abrocitinib, Upadacitinib, Lebrikizumab, Nemolizumab, Ruxolitinib, Bimekizumab, Roflumilast.
- Triamcinolone — DRUGTriamcinolone
- 5-Fluorouracil — DRUG5-fluorouracil
- Calcipotriene — DRUGCalcipotriene
- Tapinarof — DRUGTapinarof
- Crisaborole — DRUGCrisaborole
- Tacrolimus — DRUGTacrolimus
- Adalimumab — DRUGAdalimumab
- Etanercept — DRUGEtanercept
- Certolizumab — DRUGCertolizumab
- Infliximab — DRUGInfliximab
- Secukinumab — DRUGSecukinumab
- Ixekizumab — DRUGIxekizumab
- Apremilast — DRUGApremilast
- Risankizumab — DRUGRisankizumab
- Ustekinumab — DRUGUstekinumab
- Hydroxychloroquine — DRUGHydroxychloroquine
- Methotrexate — DRUGMethotrexate
- Mycophenolate — DRUGMycophenolate
- Azathioprine — DRUGAzathioprine
- Chloroquine — DRUGChloroquine
- Cyclosporine — DRUGCyclosporine
- Tofacitinib — DRUGTofacitinib
- Deucravacitinib — DRUGDeucravacitinib
- Dupilumab — DRUGDupilumab
- Tralokinumab — DRUGTralokinumab
- Guselkumab — DRUGGuselkumab
- Tildrakizumab — DRUGTildrakizumab
- Baractinib — DRUGBaractinib
- Abrocitinib — DRUGAbrocitinib
- Upadacitinib — DRUGUpadacitinib
- Lebrikizumab — DRUGLebrikizumab
- Nemolizumab — DRUGNemolizumab
- Ruxolitinib — DRUGRuxolitinib
- Bimekizumab — DRUGBimekizumab
- Roflumilast — DRUGRoflumilast
Study Details
This study is being done to test a microdevice, which is a small device designed to test drugs directly on skin conditions like atopic dermatitis (eczema) and psoriasis. The small device, about the size of a grain of rice, has up to 20 tiny reservoirs that hold medications that are approved by the Food and Drug Administration (FDA) for atopic dermatitis and psoriasis. Very small amounts of these medications will be released into the skin (at levels in your body much lower than are typically used). In this study, the device will be tested to see if it's safe and works well for predicting how the skin will react to standard treatments. We will also look at how these reactions are connected to genetic information and overall treatment results.
Key Dates
- Start date
- Aug 1, 2026
- Status verified
- Jun 2026
- Primary completion
- Jun 1, 2030
- Completion
- Jun 1, 2030
Study Design
- Enrollment
- 10 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- DEVICE_FEASIBILITY
Arms
- Experimental: In situ cutaneous microdeviceThe small device, about the size of a grain of rice, has up to 20 tiny reservoirs that hold medications that are approved by the Food and Drug Administration (FDA) for atopic dermatitis and psoriasis. Very small amounts of these medications will be released into the skin (at levels in your body much lower than are typically used). In this study, the device will be tested to see if it's safe and works well for predicting how the skin will react to standard treatments. We will also look at how these reactions are connected to genetic information and overall treatment results.
Primary Outcome Measure
Number of participants with adverse events [ Time Frame: 1 year ]
Central Contacts
- Raymond Cho, MD, PhD415-353-7800
- Jeffrey Cheng, MD, PhD415-575-0524
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of California, San Francisco | San Francisco | California | 94158 | - |
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