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PDI-320 for Rosacea
Phase 2
Waitlist Available
Research Sponsored by PreCision Dermatology, 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 baseline, week 4 and week 8
Awards & highlights
Study Summary
This 4-arm Phase 2 vehicle-controlled study is designed to assess the safety and efficacy of PDI-320, and the individual components, in adult subjects with rosacea.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, week 4 and week 8
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, week 4 and week 8
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Inflammation
Treatment "Success Rate" based on change in Investigator's Global Assessment (IGA)
Secondary outcome measures
Absolute change in inflammatory lesion count (interim time points)
Change in erythema severity
Change in telangiectasia severity
+1 moreTrial Design
4Treatment groups
Experimental Treatment
Placebo Group
Group I: PDI-320 Monad #2Experimental Treatment1 Intervention
Foam, twice daily for up to 12 weeks
Group II: PDI-320 Monad #1Experimental Treatment1 Intervention
Foam, twice daily for up to 12 weeks
Group III: PDI-320Experimental Treatment1 Intervention
Foam, twice daily for up to 12 weeks
Group IV: VehiclePlacebo Group1 Intervention
Foam, twice daily for up to 12 weeks
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Who is running the clinical trial?
PreCision Dermatology, Inc.Lead Sponsor
1 Previous Clinical Trials
151 Total Patients Enrolled
Syd Dromgoole, PhDStudy DirectorTherapeutics, Inc.
4 Previous Clinical Trials
292 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Who else is applying?
What portion of applicants met pre-screening criteria?
Did not meet criteria
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