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NCT01430312 · ClinicalTrials.gov registry record · Phase 1
21 Day Irritancy Test of Azelaic Acid Pre-foam Formulation
A Phase 1 study of Healthy, sponsored by LEO Pharma.
- Completed
- Registry status
- Phase 1
- Development phase
- 40
- Enrollment target
- 1
- Study location
NCT01430312 is a Phase 1 study of Healthy that has completed, run by LEO Pharma. The registered enrollment target is 40 participants, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01430312, a Phase 1 study of Healthy, has completed, sponsored by LEO Pharma.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 40 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine the irritancy potential of azelaic acid pre-foam formulation.
Conditions Studied
Interventions
- DRUG azelaic acid pre-foam formulation
- DRUG Vehicle pre-foam formulation
- DRUG Water
- DRUG Sodium lauryl sulfate
Study Locations (1)
North Dakota
- Robert I. Cooper, MD - Fargo
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2011-09 |
| Est. Completion | 2011-12 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01430312
The ClinicalTrials.gov registry entry for NCT01430312 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 647-participant average among 1,090 other Healthy trials with a reported enrollment target (94% lower). The listed sponsor is LEO Pharma, which has 65 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy appearing as the primary indexed condition, and to 4 interventions - of which azelaic acid pre-foam formulation is the first listed.
NCT01430312 reports 1 study location spanning 1 distinct geographic area - top geographies include North Dakota.
Frequently Asked Questions
What is clinical trial NCT01430312 about?
NCT01430312 is a clinical study titled "21 Day Irritancy Test of Azelaic Acid Pre-foam Formulation". The purpose of this study is to determine the irritancy potential of azelaic acid pre-foam formulation.
What is the current status of trial NCT01430312?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2011-09. Estimated completion is 2011-12.
What conditions does trial NCT01430312 study?
This clinical trial studies the following conditions: Healthy.
What interventions are being tested in trial NCT01430312?
The interventions under investigation include: azelaic acid pre-foam formulation (DRUG), Vehicle pre-foam formulation (DRUG), Water (DRUG), Sodium lauryl sulfate (DRUG).
Who is sponsoring clinical trial NCT01430312?
This trial is sponsored by LEO Pharma, which has 65 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01430312 being conducted?
This trial has 1 study location across North Dakota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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