A Study to Investigate the Safety and Clinical Effect of Nexagon® as a Topical Treatment for Subjects With a Diabetic Foot Ulcer (DUNE)



Status:Completed
Conditions:Gastrointestinal, Podiatry, Diabetes
Therapuetic Areas:Endocrinology, Gastroenterology, Orthopedics / Podiatry
Healthy:No
Age Range:18 - Any
Updated:5/3/2014
Start Date:July 2012
End Date:October 2013
Contact:Alexis White, BSc
Email:alexis@codanz.com
Phone:+64 9 376 0420

Use our guide to learn which trials are right for you!

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

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.


Inclusion Criteria:

1. Diagnosis of diabetes mellitus (Type I or II)

2. HbA1c of less than or equal to 12.0%

3. Diagnosis of neuropathic foot ulcer with partial or complete neuropathy

4. Cutaneous ulcer on the plantar or dorsal aspect of the foot or toe that is greater or
equal to 1.0cm2 and less than or equal to 8.0 cm2 in area at the end of the screening
period and is full thickness with no exposed ligament, tendon, joint capsule or bone.
Surface area will be measured by digital planimetry.

5. The Medical Monitor(or delegate)must confirm that the reference diabetic foot ulcer
(RDFU)is suitable for inclusion after reviewing digital photographs

6. Wound bed consisting of completely viable tissue or one where completely viable
tissue will be achieved by the end of the screening period.

7. An Ankle Branchial Index (ABI) of greater or equal to 0.80 in concert with a bi- or
tri-phasic Doppler flow pattern; or adequate circulation as demonstrated by any of
the following methods: peri-wound transcutaneous partial pressure oxygen
(TcpO2)greater or equal to 40 mmHg; or a toe pressure of greater or equal to 40 mmHg;
or skin perfusion pressure of greater or equal to 40 mmHg.

8. Ulcer present for 4 weeks or more or less than or equal to 12 months.

9. Willing to wear a Removable Cast Walker (RCW) between study visits for the duration
of the study.

10. Signed informed consent form.

Exclusion Criteria:

1. Any unstable medical condition that would cause the study to be detrimental to the
subject.

2. Decrease in RDFU size by more than 40% or increase in the ulcer size by more than 40%
during the 14-day screening period as measured by digital planimetry.

3. Ulcers caused primarily by untreated vascular insufficiency or ulcers with an
etiology not related to diabetes.4. Ulcers above the ankle.

5. Ulcers that cannot be effectively off-loaded using the cast walker and sole insert
provided in this study (ulcers not located on the weight bearing surface of the foot do
not require off-loading).

6. Ulcers on the toes not accessible for photography (e.g. in the web space). 7. Presence
of other ulcers within 2cm of the perimeter of the RDFU. 8. BMI > 45 9. Cannot tolerate or
will not comply with the off-loading method, or non-compliance with standard or care.

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.

11. Subjects presenting with the clinical characteristics of cellulitis at the ulcer site.
12. Necrosis, purulence, or sinus tracts that cannot be removed by debridement.13.
Definite or suspected osteomyelitis within any wound located anywhere on the subjects
body.14. Acute Charcot's neuroarthropathy as determined by clinical and/or previous
radiographic examination.

15. Severe Charcot deformity or rocker bottom foot with an associated plantar mid-foot or
heel ulcer.

16. Revascularization surgery on the leg with the wound to be treated less than or equal
to 4 weeks prior to the start of the screening period.

17. Requirement for concurrent topical antimicrobials to treat the RDFU after the end of
the screening period.

18. Received dermal substitute or living skin equivalent (e.g. Dermagraft® or Apligraf®)
within 14 days prior of the start of the screening period.

19. Severe complications of diabetes that in the opinion of the Investigator could
interfere with wound healing or impede the subject's participation.

20. Subjects on concurrent immunosuppressive therapy to include oral corticosteroid
therapy equivalent to greater than 5 mg/day of prednisone.

21. Any history of radiation therapy to the foot. 22. Female subjects who are pregnant or
lactating. 23. Pre-menopausal women not using effective birth control methods as
determined by the Investigator. 24. Life expectancy of < 12 months. 25. Subjects on renal
replacement therapy. 26. Cancer within the last 3 years except basal and squamous cell
carcinoma. 27. Cancer within the RDFU
We found this trial at
9
sites
?
mi
from
Phoenix, AZ
Click here to add this to my saved trials
Castro Valley, California 94546
?
mi
from
Castro Valley, CA
Click here to add this to my saved trials
?
mi
from
Fresno, CA
Click here to add this to my saved trials
Hialeah, Florida 33013
?
mi
from
Hialeah, FL
Click here to add this to my saved trials
Houston, Texas 77074
?
mi
from
Houston, TX
Click here to add this to my saved trials
Las Vegas, Nevada 89119
?
mi
from
Las Vegas, NV
Click here to add this to my saved trials
?
mi
from
Miami, FL
Click here to add this to my saved trials
South Miami, Florida 33143
?
mi
from
South Miami, FL
Click here to add this to my saved trials
Tucson, Arizona 85724
?
mi
from
Tucson, AZ
Click here to add this to my saved trials