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LEO 152020 tablet for Atopic Dermatitis

Phase 2
Waitlist Available
Research Sponsored by LEO Pharma
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
Awards & highlights

Study Summary

This trial is testing a new tablet to see if it works to treat atopic dermatitis and what the side effects are when compared with a placebo tablet. There will be a 16-week treatment period during which participants will take the tablets and visit the clinic for tests and 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

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in EASI from baseline to Week 16
Secondary outcome measures
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 Treatment1 Intervention
Participants will be asked to take tablets from Week 0 to Week 16 (end of treatment).
Group II: LEO 152020 tablet - Dose regimen 2Experimental Treatment1 Intervention
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?

LEO PharmaLead Sponsor
269 Previous Clinical Trials
188,418 Total Patients Enrolled
Medical ExpertStudy DirectorLEO Pharma
53 Previous Clinical Trials
9,856 Total Patients Enrolled
~63 spots leftby Jun 2025