Personalised Pancreatic Cancer Vaccination Therapy derived from Autologous Tumor Cells and Neoantigens

Informations projet

PanCaVax

N° de convention de subvention: 836361

DOI

10.3030/836361

Projet clôturé

Date de signature de la CE 23 Novembre 2018

Date de début 1 Decembre 2018

Date de fin 31 Mai 2019

Financé au titre de

• INDUSTRIAL LEADERSHIP - Innovation In SMEs

Coût total

€ 71 429,00

Contribution de l’UE

€ 50 000,00

Coordonné par

CYTUVAX BV
Netherlands

Periodic Reporting for period 1 - PanCaVax (Personalised Pancreatic Cancer Vaccination Therapy derived from Autologous Tumor Cells and Neoantigens)

Période du rapport: 2018-12-01 au 2019-05-31

Résumé du contexte et des objectifs généraux du projet

Today a patient diagnosed with pancreas cancer is facing a very poor perspective. Only 25% of the patients will survive the next 12 months, whereas a discouraging 6% is still alive 5 years after diagnosis.
Contrary to other cancers, hardly any progress in therapy options has been made during the last 40 years.

In 2015, there were an estimated 338,000 new cases of pancreatic cancer and 330,000 pancreatic cancer deaths worldwide. It is the only type of cancer with an annual mortality rate so close to its annual incidence rate. This mainly stems from the early development of systemic metastatic cancer and the late diagnosis.

The high medical need for an effective therapy for pancreatic cancer patients is the major driving force for CyTuVax in its PancaVax project. Pancreatic cancer patients have no real treatment options, as the cancer is resistant to current forms of therapy. Chemotherapy (Gemcitabine) provides only 3.9 – 6.1 months extension of survival. A more recent chemotherapy (Folfirinox) slightly improved the median survival rates for patients with metastatic pancreatic cancer. However, it carries severe side effects and is only suitable for patients with a good performance status.

It is CyTuVax’s ambition with PancaVax to substantially extend the life expectancy of patients with pancreatic cancer beyond 2 years and for some patients realize complete cure.

Travail effectué depuis le début du projet jusqu’à la fin de la période considérée dans le rapport et principaux résultats atteints jusqu’à présent

Technical progress and main results achieved during SME Phase 1

1. PanCaVax vaccine adjuvant
• In Q4-2018, the role of single cytokines Interleukin-2 (IL-2), Interleukin-4 (IL-4), Interleukin-12 (IL-12) and GM-CSF on the activation of various immune cells (the multi-arm part of the immune system) has been established.
• In Q1-2, 2019, it has been shown that the application of the multi-cytokine adjuvant creates the optimal conditions for powerful and comprehensive cellular anti-tumor immune responses, engaging all cellular arms of the immune system.

2. PanCaVax vaccine target
• in Q1-2 2019, new organoid lines have been established for pancreatic cancer patients from the Department of Surgery MUMC.
• organoid lines CL-17 and CL-19 that have been cultured for DNA isolation and sequencing. These lines have been sequenced to select neo-antigens and to determine the presence of common neo-antigens among patients.
• the inclusion of liposome encapsulated mRNA into a five cytokines vaccine adjuvant protects the mRNA from destruction and leads to translation of the mRNA into the protein antigens and, most probably, to an immune response.
• results showed that RNAses in the inflammatory fluid did not destroy the mRNA. The injection of the multi-cytokine adjuvant created optimal conditions for extracellular translation of mRNA.

Progrès au-delà de l’état des connaissances et impact potentiel prévu (y compris l’impact socio-économique et les conséquences sociétales plus larges du projet jusqu’à présent)

The next steps for remaining part of 2019 until 2022 are:
1. the preclinical proof of concept test,
2. the preparation for the GMP production of the adjuvant
3. as well as the preperation of vaccine target,
4. compiling application file for the approval of the clinical study.

The clinical Phase 1-2a trial with 10 patients will cover a period of 2 years, starting late 2020 at the earliest.

Financing - estimated costs:
Preclinical development - €850.000
Phase 1-2a trial - €2.500.000

Funding is aimed for through both venture capital and non-dilutive funds.

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