Improved EHDV-TAU oncolytic virotherapy
Improved EHDV-TAU oncolytic virotherapy Modality: Biologic |
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An oncolytic virus for melanoma tumors with defective interferon signaling, designed as a potent, specific and safe therapy. Promising in-vivo murine melanoma model shows potential for development as a mono or an add-on to chemotherapy or check-point inhibitors
Outline and unmet need
On Nov. 2015 the FDA approved the first oncolytic virus based treatment. Oncolytic viruses are a promising category of anti-cancer therapeutic agents that have a dual action:
- kill cancer cells directly and specifically and -
- stimulate of anti-tumor immunity.
The currently approved therapy enhances a durable response in a small subset of prostate cancer patients, leaving the majority of the patients as non-responders.
Viral characteristics such as size, genome composition, lytic abilities etc. determine the interactions of oncolytic viruses with cancer cells. There is a need for an oncolytic virus with markedly different characteristics to target the non-responding prostate cancer patients.
Our solution
- EHDV-TAU - Directed evolution enabled to develop a novel oncolytic virus,. A clone of the epizootic hemorrhagic disease virus matured on interferon-defective human prostate cells.
- EHDV-TAU - An oncolytic virus for melanoma tumors with defective interferon signaling, designed as a potent, specific and safe therapy.
Current Development Stage
- Promising in-vivo murine melanoma model shows potential for development as a mono or an add-on to chemotherapy or check-point inhibitors
Patents
Provisional patent application was filed on the novel viral agent and its use in the treatment of cancer.
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