The ASCEND Study: A Study to Investigate the Safety and Clinical Effect of Nexagon to Treat Slow Healing Diabetic Foot Ulcers

Sponsor

OcuNexus Therapeutics, Inc. (Industry)

Overall Status

Terminated

CT.gov ID

NCT00820703

Collaborator

(none)

Enrollment

Location

Duration (Months)

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Diabetic foot ulcers are sores on the feet that occur in 15% of diabetic patients some time during their lifetime. Once an ulcer develops, the risk of lower-extremity amputation is increased 8-fold in people with diabetes. New treatments that improve the number of ulcers that heal and/or speed up healing are urgently needed. Initial studies with a new drug called Nexagon® (developed by CoDa Therapeutics, Inc.) support the concept that healing of diabetic foot ulcers can be improved with topical application of Nexagon®. Further research will be undertaken to assess the safety and activity of Nexagon® when applied to diabetic foot ulcers at various doses. A proposed randomized controlled trial will randomly allocate (e.g., by the toss of a coin) 24 people with diabetic foot ulcers to Nexagon® (one of three different doses) or vehicle (substance containing no medication) to be applied to their ulcer three times over four weeks. Participants will be followed over four weeks to monitor their response to the treatment, specifically with regards to the amount of healing that occurs.

Condition or Disease	Intervention/Treatment	Phase
Diabetic Foot Ulcer	Drug: Nexagon® Drug: Nexagon® vehicle	Phase 1/Phase 2

Study Design

Study Type:

Interventional

Anticipated Enrollment :

24 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Double

Primary Purpose:

Treatment

Official Title:

A Randomized, Prospective, Double-blind, Vehicle-controlled, Dose-escalation, Single-center Study of the Safety and Clinical Effect of Nexagon® in the Treatment of Participants With Diabetic Foot Ulcers

Study Start Date :

Apr 1, 2009

Actual Primary Completion Date :

Nov 1, 2009

Actual Study Completion Date :

Dec 1, 2009

Outcome Measures

Primary Outcome Measures

To evaluate the safety and clinical effect of Nexagon® administered topically to diabetic foot ulcers. []

Secondary Outcome Measures

To select the optimal dose(s) which can be used in future trials of Nexagon® in diabetic foot ulcers []
To pilot the collection of data that may be considered useful in planning future studies of Nexagon® administered topically to diabetic foot ulcers. []

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Male or female aged 18 and older
Female subjects must be a) post-menopausal, b) surgically sterilized, c) practicing abstinence, or d) using hormonal contraceptive, intra-uterine device, diaphragm with spermicide or condom with spermicide for the duration of the study
Diabetes mellitus (type I or II) with an HbA1c < 10.0%
Diagnosis of neuropathic foot ulcer
Cutaneous, full thickness (University of Texas grade A1), below ankle surface ulcer between 0.5 and 5.0 cm2 post-debridement
A viable, granulating wound
Ulcer present for > 4 weeks prior to study entry
An ankle brachial index between 0.70 and 1.3 measured during screening or within three months prior to the Day -14 visit
Signed informed consent form

Exclusion Criteria:

Decrease or increase in the ulcer size by 30% or more during a14 day "run-in" period
Cannot tolerate the off-loading method or comply with standard-of-care
An ulcer which shows signs of clinical infection
The ulcer to be treated requires operative debridement.
An ulcer positive for β-hemolytic streptococcus upon culture.
Requirement for total contact casts
The ulcer has more than 50% slough, significant necrotic tissue, osteomyelitis, bone, tendon, or capsule exposure
Presence of an active systemic or local cancer or tumor of any kind (with the exception of non-melanoma skin cancer)
Congestive heart failure NYHA class II - IV
Coronary heart disease with STEMI, CABG, or PTCA within the last 6 months
Active osteomyelitis of the study foot
Active connective tissue disease
Acute Charcot's neuroarthropathy as determined by clinical and/or radiographic examination
Treatment with systemic corticosteroids (
Previous or current radiation therapy to the distal lower extremity or likelihood to receive this therapy during study participation
Pregnancy or lactation
eGFR < 25 mL/min
Poor nutritional status defined as an albumin < 25 g/L
Significant peripheral edema
Known prior inability to complete required study visits during study participation
A psychiatric condition (e.g., suicidal ideation) or chronic alcohol or drug abuse problem, determined from the subject's medical history, which, in the opinion of the Investigator, may pose a threat to subject compliance
Use of a platelet-derived growth factor within the 28 days prior to screening
Use of any investigational drug or therapy within the 28 days prior to screening
Any other factor which may, in the opinion of the Investigator, compromise participation and follow-up in this study