A Clinical Study of the Safety and Efficacy of MEBO Wound Ointment in Subjects With Diabetic Foot Ulcers

Status:	Completed
Conditions:	Gastrointestinal, Podiatry, Diabetes
Therapuetic Areas:	Endocrinology, Gastroenterology, Orthopedics / Podiatry
Healthy:	No
Age Range:	18 - Any
Updated:	1/12/2017
Start Date:	September 2012
End Date:	December 2013

A Phase II, Randomized, Controlled, Multi-Center Study of the Safety and Efficacy of Topically Applied MEBO Wound Ointment Compared to Standard of Care in Subjects With Diabetic Foot Ulcers

The objective of this study is to evaluate the safety and efficacy of MEBO in the treatment
of subjects with diabetic foot ulcers (DFUs).

This is a phase II, randomized, controlled, multi-center study designed to assess the safety
and efficacy of MEBO in the treatment of subjects with DFUs. Subjects meeting entry criteria
will be randomly assigned in a 1:1 ratio for up to 8 weeks of treatment with either MEBO or
SOC.

Inclusion Criteria:

- Male or female ≥18 years of age

- Able and willing to provide informed consent

- Able and willing to comply with protocol visits and procedures

- Target ulcer duration of ≥4 weeks

Exclusion Criteria:

- Ulcer of a non-diabetic pathophysiology

- Known or suspected allergies to any of the components of MEBO

- Malignancy on target ulcer foot

- Non-compliance in the screening or run-in period

We found this trial at

sites

HOPE Research Institute

Phoenix, Arizona 85050

from

Phoenix, AZ