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Not Yet RecruitingNCT07352566

Utilization of a Microdevice for Psoriasis and Atopic Dermatitis

Utilization of a Cutaneous Therapy In Situ Microdevice

Status
Not Yet Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
10 (estimated)
Sponsor
University of California, San Francisco · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

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.

Conditions

Interventions

TypeNameDescription
DEVICEIn 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. 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.
DRUGTriamcinoloneTriamcinolone
DRUG5-Fluorouracil5-fluorouracil
DRUGCalcipotrieneCalcipotriene
DRUGTapinarofTapinarof
DRUGCrisaboroleCrisaborole
DRUGTacrolimusTacrolimus
DRUGAdalimumabAdalimumab
DRUGEtanerceptEtanercept
DRUGCertolizumabCertolizumab
DRUGInfliximabInfliximab
DRUGSecukinumabSecukinumab
DRUGIxekizumabIxekizumab
DRUGApremilastApremilast
DRUGRisankizumabRisankizumab
DRUGUstekinumabUstekinumab
DRUGHydroxychloroquineHydroxychloroquine
DRUGMethotrexateMethotrexate
DRUGMycophenolateMycophenolate
DRUGAzathioprineAzathioprine
DRUGChloroquineChloroquine
DRUGCyclosporineCyclosporine
DRUGTofacitinibTofacitinib
DRUGDeucravacitinibDeucravacitinib
DRUGDupilumabDupilumab
DRUGTralokinumabTralokinumab
DRUGGuselkumabGuselkumab
DRUGTildrakizumabTildrakizumab
DRUGBaractinibBaractinib
DRUGAbrocitinibAbrocitinib
DRUGUpadacitinibUpadacitinib
DRUGLebrikizumabLebrikizumab
DRUGNemolizumabNemolizumab
DRUGRuxolitinibRuxolitinib
DRUGBimekizumabBimekizumab
DRUGRoflumilastRoflumilast

Timeline

Start date
2026-01-01
Primary completion
2030-06-01
Completion
2030-06-01
First posted
2026-01-20
Last updated
2026-01-20

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07352566. Inclusion in this directory is not an endorsement.