Pioneering precision therapies for the new era of cancer care

Reimagining cancer therapy

The EDV™ nanocell platform

The EDV™ nanocell is a first-in-class cyto-immunotherapy platform – the first bacterially derived nanocell designed to deliver precision therapy directly to the tumour and engage the patient’s own immune system.

EnGeneIC is pioneering the EDV™ as a new class of cancer therapy combining cancer cell killing with immune cell activation

EnGeneIC manufacturing laboratory

How the EnGeneIC Dream Vector (EDV™) Works

01Empty EDVs

Robust uniform empty nanocells, 400 nm in diameter, harvested from avirulent/non-pathogenic bacteria.

Cluster of empty EDV nanocells

02Uptake of payload

Load potent chemotherapy, functional nucleic acids, or immune adjuvant in separate EDVs.

Immune adjuvant EDV and payload EDV

03Attach antibody

EDVs containing a potent chemotherapy payload have antibody attached to the nanocell wall. One arm of the antibody attaches to the nanocell, the other binds to the tumour via EGFR recognition (or any other chosen antigen).

Antibody-coated EDV nanocell

04Administration

EDVs™ are IV infused over 5-10 mins. Targeted EDV™ with chemotherapy payload escape into the tumour microenvironment via leaky blood vessels caused by the tumour, to target cancer cells. Monitoring immune cells such as macrophages, dendritic cells and NK Cells take up EDVs and recognise bacterial origin of EDVs™. This stimulates fresh immune cells to be activated.

Macrophage, dendritic cell and NK cell

05Targeted tumour killing

EDVs containing potent chemotherapy payload are designed to bind to tumour cells via antibody (EGFR-directed), triggering engulfment and cell death.

Tumour cell killed by an EDV payload

06Activate anti-tumour immune response

EDVs activate an adaptive immune response by T Cells and iNKT Cells.

T cells and iNKT cells attacking a tumour cell

Lead programs

Pancreatic cancer

EDV™ cyto-immunotherapy directed at one of the hardest-to-treat solid tumours.

Recurrent glioblastoma

Designed to deliver therapy directly to brain tumours, where treatment options are limited.