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Topical Gel
PR022 topical gel, 0.05% for Atopic Dermatitis
Phase 2
Waitlist Available
Research Sponsored by Realm Therapeutics, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 29 days
Awards & highlights
Study Summary
The purpose of this study is to determine whether PR022 Topical Gels are safe and effective treatments for mild-to-moderate atopic dermatitis (AD).
Eligible Conditions
- Atopic Dermatitis
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 29 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~29 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Percent change from Baseline to Day 29 in Eczema Area and Severity Index (EASI)
Secondary outcome measures
Change from Baseline to Day 29 in 5 dimensions of itch (5-D Itch) scale
Change from Baseline to Day 29 in Dermatology Life Quality Index (DLQI)
Change from Baseline to Day 29 in SCORing Atopic Dermatitis (SCORAD)
+7 moreOther outcome measures
Body Weight Changes
Trial Design
3Treatment groups
Experimental Treatment
Placebo Group
Group I: PR022 topical gel, 0.1%Experimental Treatment1 Intervention
Applied twice daily for 28 days
Group II: PR022 topical gel, 0.05%Experimental Treatment1 Intervention
Applied twice daily for 28 days
Group III: PR022 topical gel vehiclePlacebo Group1 Intervention
Applied twice daily for 28 days
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Who is running the clinical trial?
Realm Therapeutics, Inc.Lead Sponsor
1 Previous Clinical Trials
96 Total Patients Enrolled
Christian Peters, MD, PhDStudy DirectorRealm
Frequently Asked Questions
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