Topical pexiganan cream 0.8%
Drug14 days of treatment
Other names: MSI-78
NCT Number: NCT01590758
The purpose of this study is to establish the clinical superiority and the safety of topical pexiganan cream 0.8% plus standard local wound care, as compared to placebo cream plus standard local wound care, in the treatment of mildly infected diabetic foot ulcers.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Birmingham, Alabama, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
14 days of treatment
Other names: MSI-78
14 days of treatment
14 days of treatment
Time frame: 28 days
The numbers of participants with Clinical Response, defined as resolution of infection, are reported.
Time frame: 28 days
The numbers of participants with Microbiological Response, defined as eradication of all initial pathogens, are reported.
Time frame: 28 days
The numbers of participants with TEAEs, including those with Serious TEAEs, are reported
Dipexium Pharmaceuticals, Inc.
Industry
A Randomized, Double-Blind, Multicenter, Superiority, Placebo-Controlled Phase 3 Study of Pexiganan Cream 0.8% Applied Twice Daily for 14 Days in the Treatment of Adults With Mild Infections of Diabetic Foot Ulcers
Acronym: OneStep-1
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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