MaxONCO is a 36-month project (January 2020 – December 2022), funded by the European Commission within Horizon 2020 to support the clinical development and commercialization of a cancer immunotherapy product created by MaxiVAX, a clinical stage (Phase II) Swiss biotech company working to develop best in-class therapeutics for the treatment of various cancers.
The aim of the MaxONCO project is to conduct a Phase II clinical trial in Head and Neck cancer indication and prepare for the manufacturing and commercialization of MaxONCO, MaxiVAX’s first immunotherapy product.
Head and neck cancer is one of the most common malignancies worldwide, accounting for more than 650,000 new cases and 380,000 deaths annually. Despite advances in surgical, radiation techniques, chemotherapy and monoclonal antibodies in the treatment of advanced head and neck cancer; it remains that about 50% of patients with this condition will die within 5 years.
MaxiVAX’s therapy uses the patient’s own natural addressing direct immunization against the patients’ own cancer cells, making it applicable to multiple type of cancers including head and neck cancer, and chordoma. The anti-cancer therapy consists of two components: 1) biocompatible capsules, loaded with a genetically modified cell-line that secretes a strong immune-booster GM-CSF (granulocyte macrophage colony stimulating factor) and 2) irradiated patients’ tumour cells, isolated from patients which serve as tumour antigens. To induce an efficient anti-tumour response against the patients’ own tumour cells, the encapsulated GM-CSF secreting cells are implanted subcutaneously at the site of tumour-cell vaccination.
The Phase II Head and Neck clinical trial has reached positive outcome. A clinical study report, providing the clinical and statistical analyses of the trial will be produced, as per protocol and applicable regulations. MaxiVAX is preparing clinical trials to test the new generation therapeutic product MaxONCO 2, involving a larger population to further test the efficacy of MaxONCO for this indication.