NCT07352566

Brief 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.

Trial Health

63
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for phase_4

Timeline
50mo left

Started Jan 2026

Longer than P75 for phase_4

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress8%
Jan 2026Jun 2030

First Submitted

Initial submission to the registry

November 17, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

January 1, 2026

Completed
19 days until next milestone

First Posted

Study publicly available on registry

January 20, 2026

Completed
4.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2030

Last Updated

January 20, 2026

Status Verified

January 1, 2026

Enrollment Period

4.4 years

First QC Date

November 17, 2025

Last Update Submit

January 13, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Number of participants with adverse events

    The safety of microdevice placement and removal will be based on assessment of adverse events.

    1 year

  • Proportion of retrieved devices with assessable tissue

    The feasibility of microdevice analysis based on the ability to place and retrieve the device with sufficient tissue, of sufficient quality, for downstream histopathology/molecular analysis and interpretation of at least 80% of the device reservoirs.

    1 year

Secondary Outcomes (1)

  • Change in local skin inflammation (molecular assays)

    1 year

Study Arms (1)

In situ cutaneous microdevice

EXPERIMENTAL

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.

Device: In situ cutaneous microdeviceDrug: TriamcinoloneDrug: 5-FluorouracilDrug: CalcipotrieneDrug: TapinarofDrug: CrisaboroleDrug: TacrolimusDrug: AdalimumabDrug: EtanerceptDrug: CertolizumabDrug: InfliximabDrug: SecukinumabDrug: IxekizumabDrug: ApremilastDrug: RisankizumabDrug: UstekinumabDrug: HydroxychloroquineDrug: MethotrexateDrug: MycophenolateDrug: AzathioprineDrug: ChloroquineDrug: CyclosporineDrug: TofacitinibDrug: DeucravacitinibDrug: DupilumabDrug: TralokinumabDrug: GuselkumabDrug: TildrakizumabDrug: BaractinibDrug: AbrocitinibDrug: UpadacitinibDrug: LebrikizumabDrug: NemolizumabDrug: RuxolitinibDrug: BimekizumabDrug: Roflumilast

Interventions

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. 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.

In situ cutaneous microdevice

Triamcinolone

In situ cutaneous microdevice

5-fluorouracil

In situ cutaneous microdevice

Calcipotriene

In situ cutaneous microdevice

Tapinarof

In situ cutaneous microdevice

Crisaborole

In situ cutaneous microdevice

Tacrolimus

In situ cutaneous microdevice

Adalimumab

In situ cutaneous microdevice

Etanercept

In situ cutaneous microdevice

Certolizumab

In situ cutaneous microdevice

Infliximab

In situ cutaneous microdevice

Secukinumab

In situ cutaneous microdevice

Ixekizumab

In situ cutaneous microdevice

Apremilast

In situ cutaneous microdevice

Risankizumab

In situ cutaneous microdevice

Ustekinumab

In situ cutaneous microdevice

Hydroxychloroquine

In situ cutaneous microdevice

Methotrexate

In situ cutaneous microdevice

Mycophenolate

In situ cutaneous microdevice

Azathioprine

In situ cutaneous microdevice

Chloroquine

In situ cutaneous microdevice

Cyclosporine

In situ cutaneous microdevice

Tofacitinib

In situ cutaneous microdevice

Deucravacitinib

In situ cutaneous microdevice

Dupilumab

In situ cutaneous microdevice

Tralokinumab

In situ cutaneous microdevice

Guselkumab

In situ cutaneous microdevice

Tildrakizumab

In situ cutaneous microdevice

Baractinib

In situ cutaneous microdevice

Abrocitinib

In situ cutaneous microdevice

Upadacitinib

In situ cutaneous microdevice

Lebrikizumab

In situ cutaneous microdevice

Nemolizumab

In situ cutaneous microdevice

Ruxolitinib

In situ cutaneous microdevice

Bimekizumab

In situ cutaneous microdevice

Roflumilast

In situ cutaneous microdevice

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • \> 18 years of age patients with atopic dermatitis or psoriasis if female patient with child bearing potential (on oral contraceptive pills or intrauterine device for at least 30 days)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of California, San Francisco

San Francisco, California, 94158, United States

Location

Related Publications (4)

  • Tsai LL, Phillips WW, Hung YP, Dominas C, Deans K, Ahn S, Ferland B, Weiss K, Lanuti M, Auchincloss H, Schumacher L, Jonas O, Colson YL. First-in-Human Intrathoracic Implantation of Multidrug-Eluting Microdevices for In Situ Chemotherapeutic Sensitivity Testing as Proof of Concept in Nonsmall Cell Lung Cancer. Ann Surg. 2023 May 1;277(5):e1143-e1149. doi: 10.1097/SLA.0000000000005385. Epub 2023 Apr 6.

    PMID: 35129472BACKGROUND
  • Tatarova Z, Blumberg DC, Korkola JE, Heiser LM, Muschler JL, Schedin PJ, Ahn SW, Mills GB, Coussens LM, Jonas O, Gray JW. A multiplex implantable microdevice assay identifies synergistic combinations of cancer immunotherapies and conventional drugs. Nat Biotechnol. 2022 Dec;40(12):1823-1833. doi: 10.1038/s41587-022-01379-y. Epub 2022 Jul 4.

    PMID: 35788566BACKGROUND
  • Peruzzi P, Dominas C, Fell G, Bernstock JD, Blitz S, Mazzetti D, Zdioruk M, Dawood HY, Triggs DV, Ahn SW, Bhagavatula SK, Davidson SM, Tatarova Z, Pannell M, Truman K, Ball A, Gold MP, Pister V, Fraenkel E, Chiocca EA, Ligon KL, Wen PY, Jonas O. Intratumoral drug-releasing microdevices allow in situ high-throughput pharmaco phenotyping in patients with gliomas. Sci Transl Med. 2023 Sep 6;15(712):eadi0069. doi: 10.1126/scitranslmed.adi0069. Epub 2023 Sep 6.

    PMID: 37672566BACKGROUND
  • Jonas O, Landry HM, Fuller JE, Santini JT Jr, Baselga J, Tepper RI, Cima MJ, Langer R. An implantable microdevice to perform high-throughput in vivo drug sensitivity testing in tumors. Sci Transl Med. 2015 Apr 22;7(284):284ra57. doi: 10.1126/scitranslmed.3010564.

    PMID: 25904741BACKGROUND

MeSH Terms

Conditions

PsoriasisDermatitis, Atopic

Interventions

TriamcinoloneFluorouracilcalcipotrienetapinarofcrisaboroleTacrolimusAdalimumabEtanerceptCertolizumab PegolInfliximabsecukinumabixekizumabapremilastrisankizumabUstekinumabHydroxychloroquineMethotrexateMycophenolic AcidAzathioprineChloroquineCyclosporinetofacitinibdeucravacitinibdupilumabtralokinumabguselkumabtildrakizumababrocitinibupadacitiniblebrikizumabnemolizumabruxolitinibbimekizumabRoflumilast

Condition Hierarchy (Ancestors)

Skin Diseases, PapulosquamousSkin DiseasesSkin and Connective Tissue DiseasesSkin Diseases, GeneticGenetic Diseases, InbornCongenital, Hereditary, and Neonatal Diseases and AbnormalitiesDermatitisSkin Diseases, EczematousHypersensitivity, ImmediateHypersensitivityImmune System Diseases

Intervention Hierarchy (Ancestors)

PregnadienesPregnanesSteroidsFused-Ring CompoundsPolycyclic CompoundsSteroids, FluorinatedUracilPyrimidinonesPyrimidinesHeterocyclic Compounds, 1-RingHeterocyclic CompoundsMacrolidesLactonesOrganic ChemicalsAntibodies, Monoclonal, HumanizedAntibodies, MonoclonalAntibodiesImmunoglobulinsImmunoproteinsBlood ProteinsProteinsAmino Acids, Peptides, and ProteinsSerum GlobulinsGlobulinsImmunoglobulin Fc FragmentsImmunoglobulin FragmentsPeptide FragmentsPeptidesImmunoglobulin Constant RegionsReceptors, Tumor Necrosis FactorReceptors, CytokineReceptors, ImmunologicReceptors, Cell SurfaceMembrane ProteinsPolyethylene GlycolsPolymersMacromolecular SubstancesImmunoglobulin Fab FragmentsAminoquinolinesQuinolinesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-RingAminopterinPterinsPteridinesCaproatesAcids, AcyclicCarboxylic AcidsFatty AcidsLipidsThionucleosidesSulfur CompoundsMercaptopurinePurinesNucleosidesNucleic Acids, Nucleotides, and NucleosidesCyclosporinsPeptides, CyclicMacrocyclic Compounds

Study Officials

  • Raymond Cho, MD, PhD

    University of California, San Francisco

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Raymond Cho, MD, PhD

CONTACT

Jeffrey Cheng, MD, PhD

CONTACT

Study Design

Study Type
interventional
Phase
phase 4
Allocation
NA
Masking
NONE
Purpose
DEVICE FEASIBILITY
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 17, 2025

First Posted

January 20, 2026

Study Start

January 1, 2026

Primary Completion (Estimated)

June 1, 2030

Study Completion (Estimated)

June 1, 2030

Last Updated

January 20, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations