NOX1416 in Treatment of Chronic Non-Healing Diabetic Foot Ulcers

Running, not enrolling · Phase 1

Conditions studied: Diabetic Foot Ulcer

In brief

The goal of this multi-center, randomized, controlled, evaluator-blinded study is to assess and measure the safety and efficacy of NOX1416 as an adjunct to standard of care (SOC) in the treatment of chronic, non-healing, diabetic foot ulcers (DFUs). Subjects will be randomized to receive treatment with NOX1416 as an adjunct to Standard of Care (SOC) or SOC alone. The primary objective of the study is to demonstrate the safety and tolerability of NOX1416 as adjunct to SOC. The secondary objective of the study is to evaluate the clinical benefit of daily NOX1416, as an adjunct to SOC, in the treatment of chronic, non-healing diabetic foot ulcers. The study will use a centralized blinded assessor. The blinded assessor will be responsible for assessing the efficacy endpoints such as wound measurements and complete wound closure. The blinded assessor will not be involved in the clinical care of the subject.

Key facts

Study ID

NCT06402565

Run by

NOxy Health Products, LLC

People needed

40

Starts

2024-06-06

Expected to finish

2026-06-30

Last updated by the study team

2026-05-20

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Subjects will be eligible for enrollment in the study only if they meet ALL the following criteria at time of Screening:
• Male or female subjects aged 18 to 80 years (inclusive) with Type 1 or Type 2 diabetes requiring treatment with oral medications and/or insulin replacement therapy
• Subject has a glycosylated hemoglobin, HbA1c ≤ 12%. Note: Prior documented HbA1c within the last 3 months of the Screening Visit is acceptable.
• Presence of at least one diabetic foot ulcer that meets all of the following criteria:
• A full-thickness ulcer of University of Texas Wound Classification (UTWCS) Grade IA or IIA
• At least 50% of the ulcer is located below the malleoli
• Ulcer size (area) is ≥ 1 cm2 and ≤ 10 cm2 (post-debridement at time of randomization)
• Unresponsive to standard ulcer care for ≥ 4 weeks (at time of screening)
• There is a minimum 1 cm margin between the qualifying Target Ulcer and any other ulcers on the specified foot, post-debridement)
• No exposed bone and no tunneling, undermining, or sinus tracts
• The index ulcer has a clean base and is free of necrotic debris at time of placement of treatment product.
• Index ulcer and/or index ulcer limb may have had prior infection, but infection(s) must be adequately treated and controlled as defined by IDSA Guidelines Grade level 1.
• Ulcer must be non-healing as defined as < 25% reduction in size in response to standard of care during the two-week run-in Screening Period (between the first Screening Visit and Baseline) Note: Criterion 3(i) will be evaluated at the time of randomization. If the subject has more than one qualifying diabetic foot ulcer, the ulcer designated as the Target Ulcer will be at the discretion of the Investigator.
• Adequate circulation to the affected foot as demonstrated by a dorsum transcutaneous oxygen measurement (TCOM) or a skin perfusion pressure (SPP) measurement of ≥ 30 mmHg or an ABI between 0.7 and ≤ 1.3, or TBI of >0.6 within 3 months of the first Screening Visit. The assessment may also be performed between SV1 and SV2.
• Subject does not smoke or use tobacco products.
• Subject, if female of child-bearing potential, has a negative urine pregnancy test at screening, must not be breastfeeding, and willing to use acceptable methods of contraception (birth control pills, barriers, or abstinence) throughout the study.
• Subject is able and willing to comply with study procedures and applicable dressing changes.
• Subject demonstrates cognitive and physical ability to administer the treatment as determined by the clinician. If a caregiver will administer the treatment, the caregiver must demonstrate cognitive and physical ability.
• The index ulcer has been offloaded with protocol defined offloading device throughout the study run-in period for at least 14 days prior to randomization (Run- in period defined as Screening through TV1/Randomization).
• A signed and dated informed consent form has been obtained from the subject.

You may not qualify if…

• Subjects meeting ANY of the following criteria at time of Screening will be excluded from enrollment:
• Ulcers with exposed bone or associated with osteomyelitis. Note: Osteomyelitis should be ruled out by clinical examination (probing of the wound) or X-ray findings, if necessary, by the Investigator.
• Subject has ulcers secondary to a disease other than diabetes, e.g., fungal ulcerations, malignant ulcerations, and ulcerations due to venous or arterial insufficiency, or due to hematological disorders, in the opinion of the Principal Investigator.
• Ulcer, which in the opinion of the Investigator, is suspicious for cancer.
• Subjects with a gangrenous or ischemic toe that may need to be amputated in the opinion of the Investigator.
• Body mass index (BMI) > 40kg/m2
• Methemoglobin > 5% at SV1
• Laboratory values at Screening of:
• Hemoglobin < 8.5 g/dL
• White Blood Cells (WBC) < 3.0 X 109 cells/L and > 11 x 109 cells/L
• Liver function studies [Total bilirubin, aspartate aminotransferase (AST) and alanine transaminase (ALT)] > 3x the upper limit of normal
• Albumin < 2.5 g/dL
• Renal function studies [Estimated Glomerular Filtration Rate] < 45
• Presence of any clinically significant medical condition(s) that, in the opinion of the Investigator, could interfere with wound healing, including but not limited to the following:
• Vasculitis or connective tissue disease
• Buerger's disease, Raynaud's or other peripheral vascular disease.
• Clinically significant claudication or peripheral edema on the affected limb
• Acute or unstable Charcot foot
• Aplastic anemia or sickle cell anemia
• Current sepsis
• Past or present malignancy below the knee on the same limb as the Target Ulcer;
• History of radiation at the Target Ulcer site.
• Subject is currently receiving (i.e., within 30 days of T1 visit) or scheduled to receive any of following medication or therapies during the course of the study.
• Immunosuppressants (including chronic systemic corticosteroids)
• Cytotoxic chemotherapy

Where it is running

• Advanced Foot Care — Phoenix, Arizona, United States
• AFC - Tucson — Tucson, Arizona, United States
• Solutions Medical Research — Coral Gables, Florida, United States
• Prohealth Research Center — Doral, Florida, United States
• Betancourt Research Services — Doral, Florida, United States
• Family First Medical Research Center — Hialeah Gardens, Florida, United States
• Symphony — Palm Harbor, Florida, United States
• Avita Clinical Research — Tampa, Florida, United States
• Clinical Trials of New England — Hyde Park, Massachusetts, United States
• Cutting Edge — Circleville, Ohio, United States
• IntraCare Clinical — Dallas, Texas, United States
• New Dawn Wellness and Medical Center — Houston, Texas, United States
• RITE Clinicals — Shenandoah, Texas, United States

Full record on ClinicalTrials.gov

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