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NCT06928246Active, not recruitingPhase 1

The Impact of Botox on Neuroimmune Interactions in Atopic Dermatitis

Pilot Study on Cellular and Molecular Impact of Neuroimmune Interactions in Atopic Dermatitis

Source: ClinicalTrials.gov · Last updated 6 Oct 2026

Brief summary (registry, in English)

The purpose of this study is to understand cellular and molecular interactions in the skin of participants with mild-to-moderate AD, and how botulinum toxin alters these interactions.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
8 (estimated)
First submitted
7 Apr 2025
Start date
17 Jul 2025
Primary completion date
15 Dec 2026
Lead sponsor
Daniel Kaplan
NCT number
NCT06928246

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 8
  • From 17 Jul 2025 to the primary completion date, 15 Dec 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Has had prior exposure to biologic treatments or has had prior treatment with systemic non-biologics (e.g. methotrexate) within 12 weeks
  • Has used topical therapy for treatment of AD within 4 weeks
    • Phase 2:
  • Has had prior exposure to biologic treatments or has had prior treatment with systemic non-biologics (e.g. methotrexate) within 12 weeks
  • Has used topical therapy for treatment of AD within 4 weeks

Other illness

  • Has medical comorbidity such as end stage congestive heart failure or coagulopathy that is a relative contradiction to skin biopsy procedure
  • Has medical comorbidity such as end stage congestive heart failure or coagulopathy that is a relative contradiction to skin biopsy procedure

Age

  • Age less than 18 years old
  • Age less than 18 years old

Other

  • Phase 1b:
  • Pregnant or breastfeeding
  • Patients enrolled in Phase 1
  • Pregnant or breastfeeding

Who the study is looking for

  • Phase 1b:
  • Patients 18 years or older at time of consent
  • Mild-to-Moderate AD, defined as:
  • BSA ≤ 10%
  • IGA ≤ 3
  • No past biologic therapy
  • No systemic therapy for 3 months
  • No topical therapy for treatment of AD for 4 weeks
    • Phase 2:
  • Patients 18 years or older at time of consent
  • Mild-to-Moderate AD, defined as:
  • BSA ≤ 10%
  • IGA ≤ 3
  • At least one patch of eczema of at least 5 cm in diameter
  • No past biologic therapy
  • No systemic therapy for 3 months
  • No topical therapy for treatment of AD for 4 weeks

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Pittsburgh Medical Center
Coordinator of this site? Confirm its status
PittsburghUnited StatesUnknown status
UPMC Department of Dermatology
Coordinator of this site? Confirm its status
PittsburghUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.