NEOX® CORD 1K vs Standard of Care in Non-healing Diabetic Foot Ulcers

Not Applicable

Terminated

• Conditions: Foot Ulcer, Diabetic
• Interventions: Other: NEOX® CORD 1K; Procedure: Standard of Care (Pressure Bandage)

• Registration Number: NCT02166294
• Lead Sponsor: Amniox Medical, Inc.

Brief Summary

In this randomized, multi-center, cross-over study, the efficacy and safety of NEOX® CORD 1K will be evaluated in patients suffering from non-healing diabetic foot ulcers. NEOX® CORD 1K is a cryopreserved human Amniotic Membrane and Umbilical Cord (AM/UC) matrix intended for use as a wound covering for dermal ulcers and defects. It is designated as a Human Cell \& Tissue Product (HCT/P) by the U.S. FDA.

Detailed Description

Patients identified for the study will have a non-healing diabetic ulcer, between 1-25cm² in size. The patient's wound(s) will be monitored for 2 weeks to document the wound pathology. Patients with less than 30% wound area reduction during the 2 week screening period and who meet all of the inclusion and none of the exclusion criteria, will be enrolled in the study. All patients will be assigned to a study or control group and undergo sharp debridement. NEOX® CORD 1K matrix will be applied to the treatment group on the day of debridement, covered with a wound veil, and standard dressing. Both groups will be monitored weekly, and the % decrease in wound size will be recorded at Baseline and Weeks 1, 2, 3, 4, 6, 8 and 12. If the wound is not progressing, additional application of NEOX® CORD 1K may be applied. The time to complete closure will be recorded for both groups. The study duration will be 12 weeks. Subjects in the control group that continue to suffer a non-healing wound at the week 12 visit will be offered an opportunity to cross-over to NEOX treatment and followed for an additional 12 weeks.

Study Timeline

• Study Start: 2014-06
• Study First Submitted: 2014-06-16
• Study First Submitted QC: 2014-06-16
• Study First Posted: 2014-06-18
• Primary Completion: 2015-06
• Study Completion: 2015-06
• Status Verified: 2017-06
• Last Update Submitted: 2017-06-26
• Last Update Posted: 2017-06-27

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 18

Inclusion Criteria

1. Between 18 years and 80 years of age inclusive
2. Confirmed diagnosis of Type I or Type II Diabetes
3. Males and Females diagnosed with a diabetic foot ulcer that is 1-25cm²
4. At least one foot ulcer that is UT Grade IA
5. Evidence of proper circulation which includes: An Index Ulcer defined as chronic (presence of wound for > 4 weeks) but not present for more than 52 weeks at the Screening Visit
6. The Index Ulcer is located below the malleoli on the plantar or dorsal surface of the foot
7. The Index Ulcer extends into the dermis or subcutaneous tissue with no evidence of exposed muscle, tendon, bone, or joint capsule
8. Wound is free of necrotic debris and clinical signs of infection
9. Patient has adequate circulation to the foot
10. In patients with non-compressible ankle vessels there is adequate flow to the foot.

Exclusion Criteria

1. The Index Ulcer is of non-diabetic pathophysiology and/or over an active Charcot deformity
2. The Index Ulcer is UT Grade IB or higher (worsening)
3. Gangrene is present on any part of the affected foot
4. The longest dimension of the Index Ulcer exceeds 5 cm at the Baseline Visit
5. Patient is currently receiving renal dialysis
6. Patient has a glycated hemoglobin A1c (HbA1c) level of > 12%
7. Patient has significant renal impairment
8. Chronic oral steroid use > 7.5 mg daily
9. Requiring intravenous (IV) antibiotics to treat the index wound infection
10. Patient has an ulcer within 15cm of the Index Ulcer identified for study consideration
11. Patient is receiving oral or parenteral corticosteroids, immunosuppressive or cytotoxic agents
12. Patient is Human Immunodeficiency Virus (HIV) positive or has Acquired Immune Deficiency Syndrome (AIDS)
13. Current evidence of osteomyelitis, cellulitis, or other evidence of infection including fever or purulent drainage from the wound site
14. Patient has active malignancy other than non-melanoma skin cancer
15. Patient's Index Ulcer has decreased by ≥ 30% during 2-week screening period
16. Patient has untreated alcohol or substance abuse at the time of screening
17. Pregnant women
18. Patient is currently enrolled or participated in another investigational device, drug, or biologic trial within 60 days of screening
19. Patient has allergy to primary or secondary dressing materials used in this trial
20. Patient has an allergy to amphotericin-B or Dulbecco's Modified Eagle Medium (DMEM)
21. Patient has had within the last 30 days, or is currently undergoing, or is planning for wound treatments with enzymes, growth factors, living skin, dermal substitutes or other advanced biological therapies

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Standard of Care Cross over to NEOX	Standard of Care (Pressure Bandage)	Subjects in the Standard of Care (pressure bandage) group that have not healed greater than 50% at the Week 12 visit, or have a wound that is worsening, will be offered participation in the cross-over arm of the trial. The cross-over arm of the study will be treated with NEOX CORD 1K and followed for 12 weeks.
NEOX® CORD 1K	NEOX® CORD 1K	Cryopreserved, umbilical cord allograft (NEOX® CORD 1K) with off-loading instructions.
Pressure bandage	Standard of Care (Pressure Bandage)	Standard of Care Pressure bandage with off-loading instructions
Standard of Care Cross over to NEOX	NEOX® CORD 1K	Subjects in the Standard of Care (pressure bandage) group that have not healed greater than 50% at the Week 12 visit, or have a wound that is worsening, will be offered participation in the cross-over arm of the trial. The cross-over arm of the study will be treated with NEOX CORD 1K and followed for 12 weeks.

Primary Outcome Measures

Name	Time	Method
Complete wound closure	12 weeks	Complete closure of the index wound, defined as 100% re-epithelialization as determined by the Investigator
Number of participants with adverse events	12 weeks	Number of participants with adverse events will be compared between the two groups.

Secondary Outcome Measures

Name	Time	Method
Number of applications	12 weeks	Number of applications of study product (up to 12 weeks from Baseline)
Blinded Reader Assessment	12 weeks and 24 weeks	Percent of wounds achieving complete closure per the assessment of a Blinded Reader (by blinded photograph of wound and measurement acetate).
Time to Initial Wound Closure	Up to 12 weeks or 24 weeks (Crossover)	Time to initial wound closure (Up to12 weeks from Baseline or 24 weeks for crossover group)

Trial Locations

Locations (3)

Center for Clinical Research, Inc.; 🇺🇸 Castro Valley, California, United States

Ankle and Foot Centers of Georgia; 🇺🇸 Newnan, Georgia, United States

University of Arizona; 🇺🇸 Tucson, Arizona, United States