Longitudinal Endotyping Of Atopic Dermatitis Through Transcriptomic Skin Analysis

Launched by NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES (NIAID) · Jun 27, 2022

Keywords

ClinConnect Summary

This clinical trial, called "Longitudinal Endotyping Of Atopic Dermatitis Through Transcriptomic Skin Analysis," is focused on understanding different types of atopic dermatitis (AD), a condition that causes itchy and inflamed skin. Researchers want to learn how the genes in the skin of people with mild and moderate-severe forms of AD change over time, especially when treated with standard medications. Participants will visit the clinic up to ten times, where their skin will be assessed, and samples will be taken to study the genetics and other factors related to their condition. The goal is to see how these factors differ between mild and more severe cases of AD, and how they respond to treatments like topical steroids and dupilumab, a medication for uncontrolled AD.

To be eligible for the study, participants should be at least 6 years old and have a diagnosis of chronic atopic dermatitis for at least a year. They should also agree to use a specific moisturizer regularly during the study. Non-AD participants will be included as a comparison group. Throughout the study, participants can expect to answer questions and undergo skin assessments, which will help researchers gain insights into how AD works and how it can be treated more effectively. It’s important to know that there are specific health criteria to meet for participation, so not everyone may qualify.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• All Participants:
• • 1. Participant and/or parent guardian must be able to understand and provide informed consent and assent (if applicable)
• • 2. Male or female, 6 years of age or older inclusive at the Screening Visit
• • 3. Participants must agree to apply a stable dose of a study provided topical moisturizer (Vanicream (TM)) at least twice daily between the Baseline Assessment and Day 7 Visits to a specified skin target area
• • 4. Individuals with asthma must adhere to asthma controller medication(s) for the duration of the study
• • 5. Individuals who can become pregnant, as defined in the study manual of procedures, must have a negative pregnancy test at the Baseline Assessment and Day 7 Visits if they do not self-report as pregnant.
• 6. Individuals who can become pregnant, as defined in the study manual of procedures, must meet either of the following criteria prior to Baseline Assessment:
• • 1. Willing to remain abstinent from intercourse that may result in pregnancy.
• • 2. Willing to use Food and Drug Administration (FDA) approved methods of contraception for the duration of the study
• • 7. Participant and/or parent guardian must be able to understand and complete study-related questionnaires.
• • 8. Participants must have adequate sizes of non-lesional skin on extremities or trunk.
• Non-Atopic dermatitis (AD) Participants:
• • 9. No history of AD or food allergy as diagnosed by a physician
• All AD Participants (DNAD and LTD):
• • 10. DNAD and LTD participants must have a history of chronic AD, (according to the Atopic Dermatitis Research Network \[ADRN\] Standard Diagnostic Criteria \[Appendix B\]), that has been present for at least 1 year before the Screening Visit.
• • 11. Must agree to refrain from applying topical steroid to a specified target area between the Baseline Assessment and Day 7 Visit
• DNAD Participants:
• • 12. DNAD participants must have active lesions on the upper or lower extremities or trunk of sufficient size and in the required locations, as specified in the study manual of procedures (MOP), for specimen collection at the Baseline Assessment and Steroid Initiation (Day 7) Visits.
• LTD Participants:
• • 13. Long-term dupilumab participants must be currently receiving dupilumab and must have started dupilumab treatment \>= 4 months prior to the Screening Visit
• Exclusion Criteria:
• • 1. Inability or unwillingness of a participant or parent guardian to comply with study protocol
• • 2. Have a genetic relative (e.g., parent, sibling, grandchild, half-sibling) or household member (e.g., spouse) already enrolled in the study
• • 3. Weight less than 15 kg
• • 4. Known systemic hypersensitivity to any of the excipients of the study treatments (Vanicream (TM), hydrocortisone, triamcinolone, or dupilumab)
• • 5. Have any skin disease other than Atopic dermatitis (AD) that might compromise the stratum corneum barrier (e.g., bullous diseases, psoriasis, cutaneous T cell lymphoma \[also called Mycosis Fungoides or Sezary syndrome\], dermatitis herpetiformis, Hailey-Hailey, or Darier's disease)
• • 6. Known or suspected immunosuppression, including history of invasive opportunistic infections (e.g. tuberculosis, histoplasmosis, listeriosis, coccidioidomycosis, pneumocystis, aspergillosis) despite infection resolution, or otherwise recurrent immune-compromised status, as judged by investigator
• • 7. Known history of human immunodeficiency virus (HIV) infection
• • 8. Ocular disorder that in the opinion of the investigator could adversely affect the individual's risk for study participation. Examples include, but are not limited to, individuals with a history of or active case of herpes keratitis; Sjogren's Syndrome, Keratoconjunctivitis Sicca, or Dry Eye Syndrome that require daily use of supplemental lubrication; or individuals with ocular conditions that require the regular use of ocular corticosteroids or cyclosporine
• • 9. Parasitic infection, except for vaginal trichomoniasis, within 12 months of the Screening Visit, or high risk for contracting parasitic infections (e.g. living in or traveling to endemic areas)
• • 10. History of malignancy within 5 years before the Screening Visit (completely treated in situ carcinoma of the cervix, and completely treated and resolved non-metastatic squamous or basal cell carcinoma of the skin or melanoma in situ are not exclusionary)
• • 11. History of non-malignant lymphoproliferative disorders
• • 12. History of alcohol or drug abuse within 2 years before the Screening Visit
• • 13. History of keloid formation (exclusionary for adult participants only)
• • 14. History of hypersensitivity to local anesthetics (e.g., lidocaine or Novocain), bleeding disorders, or treatment with anticoagulants or other conditions in adult participants that would make the biopsy procedure inadvisable
• • 15. History of serious life-threatening reaction to tape or adhesives
• • 16. Individuals with asthma who have required use of a systemic corticosteroid within 3 months prior to the Baseline Assessment Visit or who require a dose greater than 880 mcg/day of fluticasone propionate or equivalent inhaled corticosteroid to maintain asthma control.
• • 17. Planned major surgical procedure during study participation that could affect study participation or outcome assessment, per PI discretion
• • 18. Chronic or acute infection requiring treatment with systemic antibiotics, antivirals, antiparasitics, antiprotozoals, or antifungals within 4 weeks before the Baseline Assessment Visit, or superficial skin infection within 1 week before the Baseline Assessment Visit
• • 19. Pregnant or breast-feeding women, or women planning to become pregnant or breastfeed during the study
• • 20. Use of any systemic (oral, intravenous (IV), intramuscular (IM)) immunosuppressive/immunomodulating therapies (e.g. steroids, cyclosporine, Janus kinase inhibitors, mycophenolate, azathioprine, or methotrexate) within 4 Weeks of the Baseline Assessment Visit, or any condition that, in the opinion of the investigator, will likely require such treatment(s) during study participation
• 21. Treatment with biologics (other than dupilumab) as follows:
• • 1. Any cell-depleting agents, including but not limited to rituximab, within 6 months before the Baseline Assessment Visit, or until lymphocyte and CD 19+ lymphocyte count returns to normal, whichever is longer
• • 2. Omalizumab, Infliximab, adalimumab, golimumab, certolizumab pegol, abatacept, etanercept, anakinra within 16 weeks before the Baseline Assessment Visit for any indication
• • 3. Other biologics within 5 half-lives (if known) or 16 weeks before the Baseline Assessment Visit, whichever is longer
• • 22. Treatment with a live (attenuated) vaccine within 7 weeks before the Baseline Assessment Visit or planning to receive a live vaccine during the study
• 23. Ongoing participation in another research study involving any of the following:
• • 1. Current or planned use of an investigational drug or device.
• • 2. Current or planned use of prohibited medications or procedures
• • 3. Substantial time commitment and/or study requirements that may interfere with the participant's ability to comply with LEADS study requirements
• • 24. Use of investigational drug within 8 weeks or within 5 half-lives (if known), whichever is longer, before the Baseline Assessment Visit
• • 25. Use of topical calcineurin inhibitors (tacrolimus or pimecrolimus), topical phosphodiesterase inhibitors (crisaborale), or topical JAK inhibitors (ruxolitinib) within 1 week before the Baseline Assessment Visit
• • 26. Use of phototherapy (such as narrowband ultraviolet B \[NBUVB\], ultraviolet B \[UVB\], ultraviolet A1 \[UVA1\], psoralen + UVA \[PUVA\]) or a tanning booth/parlor within 4 weeks of the Baseline Assessment Visit.
• • 27. Treatment with bleach bath within 1 week before the Baseline Assessment Visit
• • 28. Use of a chlorinated hot tub within 1 week before the Baseline Assessment Visit
• • 29. Initiation of treatment with prescription moisturizers or moisturizers containing ceramide, hyaluronic acid, urea, or filaggrin (FLG) during the study period (participants may continue using stable doses of such moisturizers on body areas other than the target area if initiated before the Baseline Assessment Visit)
• • 1. Participants may continue using stable doses of such moisturizers on body areas other than the target area if initiated before the Baseline Assessment.
• • 2. Initiation of prescription moisturizer is not exclusionary when only applied to the face, neck, palms, or soles.
• • 30. Planned or anticipated use of any prohibited medications or procedures during study participation.
• • 31. Past or current medical problems or findings from physical examination that are not listed above, which, in the opinion of the investigator, may pose additional risks from participation in the study, may interfere with the participant's ability to comply with study requirements or that may impact the quality or interpretation of the data obtained from the study.