Diabetes Clinical Trial
Official title:
Growth Factor Gene Therapy for Wound Healing
Patients with diabetes may develop chronic wounds that respond poorly to treatment. Gene therapy with the platelet-derived growth factor-B gene has been shown to help with the healing of chronic wounds. This study will evaluate a new way to deliver the gene to the wound tissue.
Chronic wounds, such as diabetic ulcers, pressure ulcers, and venous stasis ulcers, cause
significant morbidity in millions of patients each year in the United States. Individuals
with long-standing diabetes develop both peripheral vascular disease and peripheral
neuropathy. These patients may not feel pressure from shoes or objects which can damage
their skin. Once a wound is formed, it may heal very slowly or not at all due to diabetic
complications.
Platelet-derived growth factor-B (PDGF-B) has been approved for use in diabetic ulcers.
However, delivery and maintenance of the drug at the wound site in sufficient quantities for
a sufficient period of time is a major hurdle to widespread use.
Gene activated matrix (GAM) technology offers the opportunity to place a therapeutic gene
contained within a structural matrix into a wound site. This study will evaluate the safety
and potential clinical utility of topical applications of GAM501, a gene for PDGF-B
contained within an E1-deleted adenoviral vector and formulated in a bovine type I collagen
gel. This formulation allows for the migration of wound repair cells into the structural
matrix, where they encounter the viral vector and subsequently produce the therapeutic
protein within the local wound environment.
Participants in this study will receive up to four treatments with GAM501. Participants will
be followed by multiple observations over a 6 to 7 month period.
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Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Factorial Assignment, Masking: Open Label, Primary Purpose: Treatment
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