Enrolling
A Study of LY3454738 in the Treatment of Adult Participants With Moderate-to-Severe Atopic Dermatitis
J4E-MC-FR01 - ClinicalTrials.gov - NCT05911841
The main purpose of this study is to describe the efficacy and safety of LY3454738 in adult participants with moderate-to-severe atopic dermatitis (AD).
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Trial Summary
Age Range
18 - 70 yearsConditions the trial is for
Atopic Dermatitis (Eczema)What the trial is testing?
UcenprubartCould I receive a Placebo?
YesEnrollment Goal
260Trial Dates
Jun 21, 2023 - Mar 2026How long will I be in the trial?
The study will last about 52 weeks and may include up to 19 visits.Trial Phase
IIKey Requirements
Clinical trials have inclusion and exclusion requirements to determine which individuals qualify for participation. Listed below are key requirements for this clinical trial, but there may be additional requirements to qualify.Participants Must:
Have active atopic dermatitis for over a year and include the following:
EASI score ≥ 12 at first dosing visit
vIGA-AD score ≥3 at first dosing visit
Have ≥10% of BSA involvement (per EASI BSA) at first dosing visit
Have little improvement with topical medicines
Participants Must Not:
Have any prior skin infections requiring treatment with topical corticosteroids
Have history of psoriasis
Have other infections such as Hepatitis B or C
Known allergy to study drug or any components to formulation or history of drug hypersensitivity reactions
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Clinical Trial Resources
You will complete the questionnaire on another website.YesNo