Low Strength IDP-107
DrugOnce a day for 16 weeks
NCT Number: NCT01194375
The purpose of this study is to evaluate the safety and efficacy of IDP-107 versus placebo in treating patients with acne vulgaris.
Looking for future studies?
Notify Me12 year and older
All sexes
Interventional
Phase 2
Ultranova Skincare, Barrie, Ontario, Canada
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Once a day for 16 weeks
Once a day for 16 weeks
Once a day for 16 weeks
Time frame: Baseline and 22 weeks
Time frame: Baseline and 22 weeks
Time frame: Baseline and 22 weeks
Looking for future studies?
Notify MeDow Pharmaceutical Sciences
Industry
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.
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