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2022-502888-38-00CompletedPhase 2

A Study of LY3454738 in the Treatment of Adult Participants With Moderate-to-Severe Atopic Dermatitis

J4E-MC-IMMB: A Master Protocol for Randomized, Controlled, Phase 2 Clinical Trials of Multiple Interventions for the Treatment of Adults with Moderate-to-Severe Atopic Dermatitis; J4E-MC-FR01: A Phase 2, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, 52-Week Study to Evaluate the Efficacy and Safety of LY3454738 in the Treatment of Adult Patients with Moderate-to-Severe Atopic Dermatitis

Source: EU CTIS (euclinicaltrials.eu) · Last updated 1 Jul 2026

Next steps

Brief summary (registry, in English)

To compare the efficacy of LY3454738 versus placebo as measured by EASI-75 in the treatment of biologic-and-small-molecule—naïve participants with moderate-to-severe Atopic Dermatitis

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
94 (actual)
First submitted
18 Apr 2023
Start date
25 Sept 2023
Lead sponsor
Eli Lilly & Co.
EU CT number
2022-502888-38-00

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 94
  • 16 sites in 3 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Have any prior skin infections requiring treatment with topical corticosteroids.

Other illness

  • 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.

Who the study is looking for

  • 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.

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

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (16)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
University of DebrecenDebrecenHungaryCompleted
Somogy Megyei Kaposi Mór Oktató KórházKaposvárHungaryCompleted
Allergo-Derm Bakos KftSzolnokHungaryCompleted
University Teaching Hospital MarkusovszkySzombathelyHungaryCompleted
Medmare Bt.VeszprémHungaryCompleted
Azienda Ospedaliero-Universitaria delle MarcheAnconaItalyWithdrawn
Azienda Socio Sanitaria Territoriale degli Spedali Civili di BresciaBresciaItalyWithdrawn
Humanitas Research HospitalRozzanoItalyWithdrawn
Azienda Ospedaliera Universitaria SeneseSienaItalyWithdrawn
Specderm Poznanska sp.j.BialystokPolandCompleted
Diamond Clinic Sp. z o.o.CracowPolandCompleted
Centrum Badan Klinicznych PI-House sp. z o.o.GdanskPolandCompleted
Dermoklinika-Medyczne Centrum s.c. M.Kierstan J.Narbutt A.LesiakLodzPolandCompleted
DERMED Centrum Medyczne Sp. z o.o.LodzPolandCompleted
Evimed Sp. z o.o.WarsawPolandCompleted
Medicover Integrated Clinical Services Sp. z o.o.WarsawPolandCompleted

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