21 Day Irritancy Test of Azelaic Acid Pre-foam Formulation

Completed · Phase 1

Conditions studied: Healthy

In brief

The purpose of this study is to determine the irritancy potential of azelaic acid pre-foam formulation.

Key facts

Study ID

NCT01430312

Run by

LEO Pharma

People needed

40

Starts

2011-09-01

Expected to finish

2011-12-01

Last updated by the study team

2020-04-01

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• healthy volunteers
• male ore female subjects
• aged 18 - 65 years
• ability to understand and fulfill the study requirements

You may not qualify if…

• affected skin in designated test area
• pregnancy or lactation
• not willing to comply with study requirements

Where it is running

• Robert I. Cooper, MD — Fargo, North Dakota, United States

Full record on ClinicalTrials.gov

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