Diabetic Foot Ulcer, Pseudomonas Aeruginosa Infection, Staphylococcus Aureus Infection, Acinetobacter Infection
Conditions
Keywords
Bacteriophage therapy
Brief summary
This is a Phase I/IIa trial designed to evaluate topical bacteriophage therapy in patients with diabetic foot ulcers.
Detailed description
The primary objective of this study is to evaluate the safety of a topical bacteriophage cocktail in the treatment of non infected and infected diabetic foot ulcers with Pseudomonas aeruginosa, Staphylococcus aureus and/or Acinetobacter baumanni. Patients will also be evaluated for bacterial clearance and wound reduction.
Interventions
BIOLOGICALTP-102
One mL of IP solution will be applied topically per cm3 of target ulcer. The titer of each bacteriophage in TP 102 is 1x10\^9 plaque forming units per milliliter (PFU/mL).
Sponsors
VectorB2B
Technophage, SA
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
Both cohorts: * Type 1 or type 2 diabetes mellitus with glycated hemoglobin (HbA1c) ≤10, 5% * Suitable physical and mental health as determined by the investigator based on medical history and general physical examination. * Subjects must be medically stable based on clinical laboratory tests, medical history and vital signs. Clinical laboratory tests should be within normal values or not clinically significant, unless directly related to the condition of diabetes. * Female subjects must fulfil one of the following criteria: 1. At least 1 year post-menopausal (amenorrhea \>12 months prior to screening); 2. Surgically sterile (bilateral oophorectomy or hysterectomy); 3. If of childbearing potential, must agree to use a highly effective method of birth control from screening until 14 days after the last administration of IP. * Female subjects of childbearing potential must have a negative pregnancy test at screening. * Male subjects with a female partner of child-bearing potential or pregnant partner must agree to use a condom from screening until 14 days after the last IP application. * ICF signed voluntarily before any study-related procedure is performed, indicating that the subject understands the purpose of, and procedures required for the study and is willing to participate in the study. Part A: \- Non-infected diabetic foot ulcer perfusion grade 1, depth grade 1 and infection grade 1 according to PEDIS classification. Part B * Infected diabetic foot ulcer meeting perfusion grade 1 or 2, depth grade 1 or 2 and infection 2 or 3,except if presence of abscess, fasciitis, osteomyelitis, and septic arthritis, according to PEDIS definition. * Infected with at least one bacterial strain susceptible to bacteriophage cocktail assessed from culture.
Exclusion criteria
Both cohorts: * Study ulcer less than 2 cm away from other ulcers in case of multiple ulcers. * History in the 5 previous years of any cancer requiring systemic chemotherapy or radiation. * A condition that, in the opinion of the Investigator, could compromise the well being of the subject or course of the study, or prevent the subject from meeting or performing any study requirements. * Immunocompromised subjects due to illness, organ transplant, or immune suppressive therapies (e.g. oral or parental corticosteroids, methotrexate, immune modulators) 3 months prior to screening. Ad hoc low dose inhaled corticosteroids or topical corticosteroids are not allowed from 2 weeks prior to randomization. * Being pregnant or breastfeeding. * Currently participating in another clinical trial or having participated in a previous clinical trial with receipt of an investigational product within 30 days of the first administration of IP or 5 half-lives, whichever is longer. * Subjects that, in the opinion of the Investigator or their treating physician, are dependent of the following therapies for their ulcer treatment: * Topical antimicrobial treatment (including isobetadine gel/dressing, silver nitrate dressing, topical antibiotic) * Enzymatic, autolytic, maggot debridement * Any active wound healing products (e.g., Dermagraft, Apligraf, Regranex, or Tegaderm hydrogel or others.) * Physical or cleansing modalities, antiseptics, corticosteroids, growth factors, solutions other than sterile normal saline and ulcer treatments. Part A: \- Clinically infected ulcers Part B: * Suspected or confirmed abscess, fasciitis, osteomyelitis or septic arthritis. * Subjects meeting grade 3 or above PEDIS perfusion criteria * Planed or anticipated surgery after screening
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 1. Incidence and severity of treatment-emergent solicited local and systemic AEs and relationship to IP from first administration until 1 week after end of treatment (EOT) (end of study -EOS) | 1 week | Local AEs include erythema/redness, swelling/induration, pain and tenderness Systemic AEs include fatigue, myalgia, fever, headache and gastrointestinal symptoms (nausea, vomiting, diarrhea) |
| 2. Incidence and severity of treatment-emergent unsolicited AEs and relationship to IP from first administration until EOS. | 1 week | — |
| 3. Incidence and severity of treatment-emergent SAEs and relationship to IP from first administration until EOS. | 1 week | — |
Secondary
| Measure | Time frame |
|---|---|
| Proportion of subjects with significant reduction or eradication from baseline in microbiologic data via culture (cfu) at d3, d8, d15, d22, d26 and EOS | 35 days |
| Changes in wound/ulcer healing from to baseline in terms of wound complete closure and partial closure (25%, 50% and 75%) at EOT. | 35 days |
| Time (days) to significant reduction or eradication of target bacteria via culture. | 35 days |
| Changes in wound/ulcer healing from to baseline in terms of wound size and depth (cm^3) at EOT. | 35 days |
Countries
Israel
Outcome results
None listed