Nexagon® Low Dose
DrugTwice weekly, topical application of Nexagon® low dose in addition to a Removable Cast Walker
NCT Number: NCT01490879
This study is for Type I or Type II diabetic subjects with with a diabetic foot ulcer. The study is being done to determine if Nexagon® plus standard of care is more effective than placebo plus standard of care. Standard of care will include debridement of the ulcer, standardized dressings and standardized off-loading using a Removable Cast Walker.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Kemerovo Regional Clinical Hospital, Kemerovo, Russia
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
10.The RDFU is infected (clinical assessment of infection)and/or biopsy proof of greater than 100,000 organisms per gram of tissue during the screening period.
Twice weekly, topical application of Nexagon® low dose in addition to a Removable Cast Walker
Twice weekly, topical application of Nexagon® medium dose in addition to a Removable Cast Walker
Twice weekly, topical application of Nexagon® high dose in addition to a Removable Cast Walker
Twice weekly, topical application of Nexagon® vehicle in addition to a Removable Cast Walker
Time frame: Within 12 weeks
Time frame: Within 12 weeks
Time frame: Within 12 weeks
Time frame: 12 weeks
Time frame: 12 weeks post-closure
Time frame: 12 weeks
OcuNexus Therapeutics, Inc.
Industry
A Randomized, Prospective, Double-blind, Vehicle-controlled, Dose-ranging, Multi-center Study to Assess the Safety and Clinical Effect of Nexagon® in the Treatment of Subjects With a Diabetic Foot Ulcer
Acronym: DUNE
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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