VESSL Therapeutics


Developer of autologous cell- and gene-based therapies for vascular-related conditions. The company isolates a patient’s endothelial cells from a short vein segment, modifies them with angiogenic genes ex vivo, and reintroduces them to promote blood-vessel formation or to line biosynthetic vascular grafts. Lead programs target peripheral artery disease and hemodialysis vascular access; preclinical work and early-phase clinical studies have been completed and further clinical progression is planned.

Industries

biotechnology
health-care
therapeutics

Nr. of Employees

small (1-50)

VESSL Therapeutics

Colab Square Facility, 6 HaYozma Street, Yokneam Illit 2069203, Israel


Products

MultiGeneAngio (autologous cell and gene therapy) for peripheral artery disease

An autologous cell-and-gene therapy that uses a patient’s endothelial cells modified ex vivo with angiogenic genes to enhance collateral artery formation and improve limb perfusion in advanced PAD/critical limb ischemia patients.

MultiGeneGraft (biosynthetic vascular graft lined with autologous cells)

A biosynthetic arterio-venous graft lined with a patient’s own gene-modified endothelial cells intended for hemodialysis vascular access to improve graft biocompatibility and durability.

Platform programs in preclinical development

Platform-derived programs under preclinical development include coronary artery disease therapy, liver regeneration therapy, and ocular therapy for diabetic retinopathy.

Expertise Areas

  • Autologous cell and gene therapy
  • Therapeutic angiogenesis
  • Vascular graft design and biomaterials
  • Preclinical and early-stage clinical development
  • Show More (2)

Key Technologies

  • Endothelial cell isolation and culture from vein segments
  • Ex vivo gene modification of primary vascular cells
  • Angiogenic gene delivery
  • Biosynthetic vascular graft fabrication and cell seeding
  • Show More (2)

News & Updates

Preclinical experiments and two Phase I/IIa clinical trials treating 35 PAD patients were completed with no reported safety issues and early indications of efficacy.

Closed a $16 million financing round to advance development of cell and gene therapy programs and support regulatory activities.


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