The Education and Research Foundation, Inc.
Lynchburg, Virginia, 24501, United States
NCT Number: NCT00680095
The purpose of this study is to determine the cumulative irritation potential of the products listed by the Sponsor.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Phase 1
Lynchburg, Virginia, 24501, United States
Healthy, adult volunteers of either sex will be patched on his/her back with AN2690 Solution 2.5%, AN2690 Solution 5%, AN2690 Solution 7.5%, AN2690 Solution Vehicle and Sodium Laurel Sulfate 0.5% over the course of 21 consecutive days. After 24 hours, the patches are to be removed and the site evaluated using a five-point scale for irritation.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
AN2690 Solution, 2.5%, Daily for up to 21 days
AN2690 Solution, Vehicle, Daily for up to 21 days
Sodium Lauryl Sulfate, 0.5%, Daily for up to 21 days
Time frame: Daily for 21 days
Pfizer
Industry
21-day Cumulative Irritation Test
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06175013
Bacterial Infections and Mycoses, Dermatomycoses
Quatres Bornes, Mauritius
View Trial DetailsNCT05202366
Bacterial Infections and Mycoses, Dermatomycoses
Fort Worth, Texas, United States
View Trial DetailsNCT00233493
Bacterial Infections and Mycoses, Dermatomycoses
Cleveland, Ohio, United States
View Trial DetailsNCT05626270
Bacterial Infections and Mycoses, Dermatomycoses
Melbourne, Florida, United States
View Trial Details