Exploring the Effect of Fespixon Cream for the Treatment of Diabetic Foot Ulcers (TEXAS 3A, 3B)

• Status: Not yet recruiting
• Trial end date: 2023-12-31
• Target enrollment: 0
• Participant gender: All

Summary

A Research Study to evaluate the therapeutic effect of Fespixon cream in patients suffering from DFU (UTWCS Grade III-A or III-B) by measuring the change of grade of UTWCS (University of Texas Diabetic Wound Classification system), wound area reduction, infection control, and incidence of treatment-emergent adverse event (TEAE).

• Phase: Phase 4
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Oneness Biotech Co., Ltd.
• Collaborator: China Medical University Hospital

Criteria

Inclusion Criteria:

1. Subjects, male or female, aged 20 to 80 years (inclusive) with Type 1 or Type 2 diabetes undergoing therapy for glycemic control using available diabetes drugs including insulin.

2. Subject has a glycosylated hemoglobin, HbA1c ≤ 12%.

3. Presence of at least one diabetic foot ulcer that meets all of the following criteria:

1. A full-thickness ulcer of UTWCS Grade III-A or III-B

2. Ulcer size (area) is >2 cm2 and ≤20 cm2 (post-debridement at time of enrollment)

3. Ulcer is located on or below the malleoli.

4. Ulcer presents for >1 week (at time of enrollment).

5. There is a minimum 3 cm margin between the qualifying Target Ulcer and any other ulcers on the specified foot, (post-debridement).

6. The infection severity of the target ulcer is defined as uninfected, mild, or moderate infection by IDSA/ IWGDF Guidelines. (IDSA/IWGDF-defined severe infection would be excluded)

Note:

• If the subject has more than one qualifying diabetic foot ulcer, the most severe ulcer will be designated as the target ulcer; meanwhile, the depth of the wound will the consideration prior to the area of the wound.

• Any foot infection with the following signs of a systemic inflammatory response syndrome is defined as severe infection according to IDSA Infection Severity. This response is manifested by two or more of the following conditions:

1. temperature>38℃ or <36℃

2. heart rate > 90 beats/minute

3. respiratory rate > 20 breaths/minute or PaCO2 < 32 mmHg

4. WBC ( white blood cell count ) < 4.0 X 109 cells/ L； > 12.0 X 109 cells/ L or ≥ 10% immature (band) forms.

4. Subject has adequate vascular perfusion of the affected limb, confirmed by Ankle-Brachial Index (ABI) ≥ 0.8 and < 1.3, or transcutaneous pressure of oxygen (TcPO2) ≥ 30 mmHg on at least one lead to ensure no serious embolisms / no serious clogging of blood vessels.

5. Subject, if female of child-bearing potential, have a negative serum/urine pregnancy test at screening, must not be breastfeeding, and willing to use 2 medically accepted methods of contraception (e.g., barrier contraceptives [female condom, or diaphragm with a spermicidal gel], hormonal contraceptives [implants, injectable, combination oral contraceptives, transdermal patches, or contraceptive rings], and intrauterine devices) during the course of the study (excluding women who are not of childbearing potential and/or who have been sterilized).

6. Subject is willing to use an off-loading device for the target ulcer on the plantar while ambulation for the duration of the study; the study institution will provide the off-loading devices.

7. Subject / identified caregiver trained on the study procedures is able and willing to comply with study procedures.

8. A signed and dated informed consent form has been obtained from the subject prior to any study-related procedures being performed.

Exclusion Criteria:

1. Other laboratory values at Screening of:

1. Liver function studies [Total bilirubin, aspartate aminotransferase (AST), and alanine transaminase (ALT)] > 3x the upper limit of normal

2. Albumin < 2.5 g/dL

3. Renal function studies [Serum Creatinine and Urea] > 3x the upper limit of normal

2. Presence of any clinically significant medical condition(s) in medical history during the screening period that, in the opinion of the investigator, could interfere with wound healing, including but not limited to the following:

1. Acute or unstable Charcot foot

2. Current sepsis

3. Active malignant disease. A subject, who has had a malignant disease in the past, was treated, and is currently disease-free, may be considered for study entry

4. Acquired immune deficiency syndrome (AIDS) or HIV positive

3. Has a known hypersensitivity to any of the investigational drug or the related components

4. X-ray or MRI scan is as a mandatory screening to rule out osteomyelitis

5. Subject is currently receiving (i.e., within 30 days of enrollment visit) or scheduled to receive any of the following medication or therapies, which could interfere with wound healing during the course of the study.

1. immunosuppressant (including chronic systemic corticosteroids)

2. cytotoxic chemotherapy

3. cytostatic therapy

4. autoimmune disease therapy

5. lower limb revascularization surgery (e.g., angioplasty, artery bypass surgery)

6. growth factors

7. hyperbaric oxygen therapy

8. bioengineered tissue or skin substitutes (ADM)

9. application of topical steroids to the ulcer

10. use of any investigational drug(s)

6. A psychiatric condition (e.g., suicidal ideation), current or chronic alcohol or drug abuse, determined from the subject's medical history, which, in the opinion of the investigator, may pose a threat to subject compliance.

7. Subjects who need to stand continuously for more than 4 hours/day and have difficulty complying with off-loading instructions.

8. Has any other factor which may, in the opinion of the investigator, compromise participation and/or follow-up in the study.