Gene therapy injection aims to heal diabetic foot sores
NCT ID NCT07391319
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This Phase 3 trial is testing a drug called Neovasculgen, given as injections into the leg muscles, to see if it can help heal foot ulcers in people with diabetes. The study will include 144 adults with type 1 or type 2 diabetes who have a non-healing foot ulcer. Participants will receive either Neovasculgen or a placebo, and researchers will track how many ulcers heal completely within about 6 months.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Neovasculgen (a gene therapy drug given as injections into the leg muscles)
- What this could lead to
- If it works, this could provide a new treatment option to help heal stubborn foot ulcers in people with diabetes, potentially reducing the risk of amputation.
- What could go wrong
- This is still an early-stage Phase 3 trial with only 144 participants, so results may not apply to everyone. The drug is injected into the muscle and may cause side effects like pain or swelling.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 144 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2025
- Expected to finish
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Mar 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Male and female patients aged 18 years and above inclusive (at the time of study entry) with neuroischemic form of diabetic foot syndrome. 2. Type 1 or type 2 diabetes mellitus. 3. Prolonged non-healing ulcerative defect on the background of standard therapy (at least 1 month), limited to the foot. 4. Depth of ulcer defect according to Wagner Scale- 1 or 2 degrees. 5. Oxygen tension in the tissues directly adjacent to the ulcer defect area, from 20 to 45 mm Hg. 6. Patients with no urgent indications for limb amputation. 7. Acceptable ankle- brachial index range of 1.3-0.25. 8. Patient's willingness to comply with the requirements for examination and treatment. 9. Availability of written informed consent from the patient. 10. Patient's consent to follow the regimen of unloading the affected area throughout the study (for patients with plantar ulcer location) Exclusion Criteria: 1. Age under 18. 2. Chronic ischemia of the lower limbs of non-atherosclerotic (other than diabetes mellitus) origin: vasculitis, systemic connective tissue diseases, Buerger's disease, congenital anomalies and vascular injuries, embolism. 3. Calcaneal localization of the ulcer. 4. Neuropathic form of diabetic foot syndrome. 5. Severe neuroosteoarthropathic deformity of the foot or other deformity that has a significant impact on the healing process. 6. Ischemia, threatening limb loss. 7. Presence of clinical signs of an infectious process in the ulcer area that is not controlled by the ongoing antibacterial therapy. 8. Presence of purulent-destructive lesions of the foot (abscess, phlegmon, osteomyelitis, etc.). 9. Skin changes associated with venous pathology. 10. Proliferative and terminal stages of diabetic retinopathy. 11. The level of glycated hemoglobin at the entrance to the study is more than 11%. 12. Diabetic ketoacidosis or diabetic precoma. 13. Systemic use of glucocorticosteroids and/or other immunosuppressive drugs within the last 30 days before inclusion in the study. 14. Recent (less than 1 month) surgery or endovascular intervention on the arteries of the lower extremities or recent (less than 1 month) deep vein thrombosis of the lower extremities. 15. Recent (less than 3 months) cases of acute myocardial infarction, unstable angina, coronary artery bypass grafting or stenting of the coronary arteries, stroke or transient ischemic attacks. 16. Planned major surgery in the next 6 months. 17. Severe concomitant disease with life expectancy less than one year. 18. Infectious diseases, septic conditions, HIV infection. 19. Diagnosis of cancer within the last 5 years. 20. Pregnancy, breastfeeding period. 21. Positive pregnancy test in women of reproductive age. 22. Alcohol or drug addiction. 23. Any other disease (including mental) or clinical condition that, in the opinion of the researcher, may affect the patient's ability to participate in the study.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Botkin Hospital
RECRUITINGMoscow, Russia
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