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LEO 152020 tablet for Atopic Dermatitis

Phase 2
Waitlist Available
Research Sponsored by JW Pharmaceutical
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Are you at least 18 years old?
Have you had atopic dermatitis for at least a year?
Timeline
Screening 3 weeks
Treatment Varies
Follow Up week 0 to week 16+3 days

Summary

This trial is testing a new pill called LEO 152020 to see if it helps adults with moderate to severe atopic dermatitis. The study will compare the new pill to another pill and check for any side effects. Participants will take the pill for several months and visit the clinic periodically for evaluations.

Eligible Conditions
  • Atopic Dermatitis

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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You must be 18 or older to participate.
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You have had eczema for at least one year.
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You have moderate to severe atopic dermatitis, as diagnosed by a doctor.
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Is your eczema present on at least 5% of your body? To help you understand, imagine that the palm of your hand is about 1% of your body surface area. So, is your eczema covering an area that's about the size of 5 hands?
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Have you used a cream containing corticosteroids to treat your skin condition in the last 6 months, but it did not help improve your condition?
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You haven't already tried at least three different types of treatments (like pills or injections) for your AD.
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Have you ever had an irregular heartbeat?
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You are not currently involved in another study testing a new treatment.
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You are not currently pregnant or nursing a baby.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~week 0 to week 16+3 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and week 0 to week 16+3 days for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in EASI From Baseline to Week 16
Secondary study objectives
Number of Adverse Events From Baseline to Week 16+3 Days Per Subject

Trial Design

4Treatment groups
Experimental Treatment
Placebo Group
Group I: LEO 152020 tablet - Dose regimen 3Experimental Treatment2 Interventions
Participants will be asked to take tablets from Week 0 to Week 16 (end of treatment).
Group II: LEO 152020 tablet - Dose regimen 2Experimental Treatment2 Interventions
Participants will be asked to take tablets from Week 0 to Week 16 (end of treatment).
Group III: LEO 152020 tablet - Dose regimen 1Experimental Treatment1 Intervention
Participants will be asked to take tablets from Week 0 to Week 16 (end of treatment).
Group IV: LEO 152020 placebo tabletPlacebo Group1 Intervention
Participants will be asked to take tablets from Week 0 to Week 16 (end of treatment).

Find a Location

Who is running the clinical trial?

JW PharmaceuticalLead Sponsor
75 Previous Clinical Trials
42,908 Total Patients Enrolled
LEO PharmaIndustry Sponsor
271 Previous Clinical Trials
188,656 Total Patients Enrolled
Medical ExpertStudy DirectorLEO Pharma
55 Previous Clinical Trials
10,095 Total Patients Enrolled
~56 spots leftby Nov 2025
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