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21 Day Irritancy Test of Azelaic Acid Pre-foam Formulation

NCT01430312 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2020-04-01

No results posted yet for this study

Summary

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

Conditions

  • Healthy

Interventions

DRUG

azelaic acid pre-foam formulation

DRUG

Vehicle pre-foam formulation

DRUG

Water

DRUG

Sodium lauryl sulfate

Sponsors & Collaborators

  • Bayer

    collaborator INDUSTRY

  • LEO Pharma

    lead INDUSTRY

Principal Investigators

  • Bayer Study Director · Bayer

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2011-09-30
Primary Completion
2011-12-31
Completion
2011-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01430312 on ClinicalTrials.gov