A Feasibility Trial to Investigate the Safety and Between-group Effect Size of STIMULAN VG and Standard of Care (SoC) in Participants With Diabetic Foot Osteomyelitis (BLADE-VG2)

Biocomposites Ltd

Status and phase: Active, not recruiting; Phase 2

Conditions: Diabetic Foot Osteomyelitis

Treatments: Drug: STIMULAN VG; Drug: Systemic Antibiotics

Study type: Interventional

Funder types: Industry

Identifiers

NCT05539963

254915

Details and patient eligibility

About

The purpose of this trial is to evaluate the safety and between-group effect size of STIMULAN VG compared to SoC treatment in patients with diabetic foot osteomyelitis (DFO).

Full description

This trial is an open-label, multi-center, randomized, controlled feasibility trial.

All participants will undergo surgical debridement and receive either STIMULAN VG and an abbreviated course of systemic antibiotic therapy (3 days ±2 days) or a full course (4-6 weeks) of systemic antibiotic therapy.

The total duration of study is Approximately 55 weeks.

Enrollment: 61 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

Participants are eligible to be included in the trial only if all of the following criteria apply:

1. Participant must be ≥18 years of age inclusive, at the time of signing the informed consent

2. Participant has a current diagnosis and is being treated for diabetes mellitus, type 1 or type 2

3. Participant who has confirmed presence of DFO (to include all bones below the ankle including the talus and calcaneum) as evidenced by at least 3 out of 5 of the following:

   1. Positive PTB test
   2. Presence of draining sinus presumed to be from underlying bone
   3. Plain X-ray or MRI scan highly suggestive of or most compatible with osteomyelitis
   4. Ulcer present for greater than 30 days
   5. Substantially elevated serum marker for inflammation (e.g. ESR >70 mm/hr and C-reactive protein >14mg/L or at least 40% higher than upper limits of normal value used at the investigational site)

4. Participant who requires surgical debridement OR Participant requiring amputation and/or resection where residual osteomyelitis remains that necessitates further surgical debridement

5. All genders are eligible to participate if they are not pregnant, not breastfeeding, are not of childbearing potential or they agree to follow contraceptive guidance

6. Subject or legal authorized representative able to provide, voluntary, signed and dated informed consent prior to any study related procedures

Exclusion criteria

Participants are excluded from the trial if any of the following criteria apply:

1. Osteomyelitis in any location other than the foot (i.e. excluding any bones located proximal to the foot)

2. Osteomyelitis of the distal phalanx (toe tip) of the great toe or lesser toes

3. Charcot foot or other deformities where the investigator believes adequate offloading is not possible

4. Severe diabetic foot infection (grade 4) in accordance to IDSA/IWGDF criteria (Appendix 6)

5. Moderate to severe reduction in renal function, defined as estimated glomerular filtration rate (eGFR) of < 30.0 ml/min/1.73 m2 (Formula for calculating eGFR: 2021 CKD-EPI Creatinine).

6. Significant peripheral arterial disease:

   • Ankle brachial index ≤ 0.7 mm Hg OR
   • toe pressure ≤ 40 mm Hg OR
   • transcutaneous oximetry ≤ 40 mm Hg

7. Hemoglobin A1c (HbA1c) > 12%

8. Contra-indication or inability to undergo an MRI scan

9. Malignancy that might affect trial interpretation of outcomes or the participant's ability to complete the trial

10. Participant who is severely immunocompromised or has received high dose corticosteroids (>10 mg prednisone (or corticosteroid equivalent) for more than 14 consecutive days within the 90 days prior to informed consent)

11. Any conditions with known hypercalcemia (> 10.3 mg/dl) or posing a significant risk for developing hypercalcemia (i.e., Hyperparathyroidism)

12. Patients with active COVID-19 will be excluded from enrollment until they are able to undergo the surgical procedure

13. Current or recent history (within last 2 years) of active substance abuse (e.g. recreational drugs, narcotics, or alcohol) that, in the judgment of the investigator, may compromise the ability of the trial participant to adhere to the trial conduct and procedures

14. Previous history of adverse incidents, allergy or contra indications (e.g. Myathesia Gravis) to any component of the investigational product, such as calcium sulfate, glycopeptide antibiotics (vancomycin), or aminoglycoside antibiotics (gentamicin)

15. Concurrent involvement in a trial of another investigational product

16. The Investigator believes trial participation may compromise safety of the participant or the results of the trial

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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61 participants in 2 patient groups

STIMULAN VG

Experimental group

Description:

Participants will receive STIMULAN VG on Day 1 following surgical debridement. Systemic antibiotics for 3 days ± 2 days following the debridement surgery.

Treatment:

Drug: Systemic Antibiotics

Drug: STIMULAN VG

Standard of Care

Active Comparator group

Description:

Participants will receive Systemic antibiotics for 4-6 weeks following the debridement surgery.

Treatment:

Drug: Systemic Antibiotics