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Boosting immuno-oncology strategies with innovative immuno-stimulants derived from bacteria, to be administrated in combination with therapeutic monoclonal antibodies

Project description

Novel immunotherapies to boost antibodies' potency against cancer

French company HEPHAISTOS-Pharma is developing innovative break-through immunotherapies able to treat patients with cold tumours, and to potentiate monoclonal antibodies used in anti-cancer therapies. The company has established several proofs-of-concept in various animal models against lymphoma, osteosarcoma, and colorectal cancer. The current strategy is to accelerate the development of these products to be used as add-ons for existing immunotherapies, increasing response rates of the patients, and achieving complete remissions. The EU-funded ONCO-BOOST project aims to validate the feasibility of the project in terms of industrial, regulatory and commercial aspects. The next steps will consist in obtaining regulatory validation, industrial scale-up and entering clinical phases to demonstrate safety and efficacy of this novel immunotherapy in humans.

Objective

Passive immunotherapies are widely used in anti-cancer therapies. However, on average the patient response rates are still weak (20%), and the cure rate without relapse are even lesser (10%). In addition, significant differences exist according to patients, and tumor types. HEPHAISTOS-Pharma develops active and non-specific immunotherapies able to potentiate commercialized antibodies, turning cold tumors hot, thus becoming accessible to immunology. We already obtained an impressive proof of concept on two animal models, first by association with Rituximab for lymphoma, then in monotherapy for osteosarcoma. Our strategy aims at developing our products for open use, as add-on for existing immunotherapies, in order to drastically increase response rates and complete remission. With this aim, we have to test our immunotherapy combined to other monoclonal antibodies commercialized in the relevant cancer models, in parallel to our developments in lymphoma. As soon as the target indication will be defined, we will start the clinical research phase I, in order to demonstrate safety, and define the efficient dose for our immunotherapy. A clinical Phase IIa, combined with Rituximab will be performed, to obtain efficacy data. Our immunotherapy will work in synergy with numerous commercialized therapeutic antibodies, and we will look for strategic deals with the main market leaders.

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Programme(s)

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Topic(s)

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Funding Scheme

Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.

SME-1 - SME instrument phase 1

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Call for proposal

Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.

(opens in new window) H2020-EIC-SMEInst-2018-2020

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Coordinator

HEPHAISTOS-PHARMA
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 50 000,00
Address
21 RUE JEAN ROSTAND
91400 Orsay
France

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SME

The organization defined itself as SME (small and medium-sized enterprise) at the time the Grant Agreement was signed.

Yes
Region
Ile-de-France Ile-de-France Essonne
Activity type
Private for-profit entities (excluding Higher or Secondary Education Establishments)
Links
Total cost

The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.

€ 71 429,00
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