Macrophage-based immunotherapy of platinum-resistant ovarian cancer
The MACOV project aims to develop a groundbreaking macrophage-based therapy for platinum-resistant ovarian cancer, preparing it for Phase I clinical trials through comprehensive pre-clinical efficacy and safety studies.
Projectdetails
Introduction
Resistance to platinum-based chemotherapy is a major clinical challenge in ovarian cancer. About 300,000 women are diagnosed with ovarian cancer each year, and the number of deaths is estimated at 180,000 worldwide annually. Ovarian cancer metastasizes early in its development, often before it's diagnosed.
Treatment Overview
Ovarian cancer treatment involves surgery with frontline platinum-based chemotherapy. As many as 15-30% of patients with ovarian cancer have primary platinum-resistant or refractory disease. The recurrence of ovarian cancer is now considered a sign of an incurable disease, as it becomes platinum-resistant.
Project Description
The project MACOV aims to develop an innovative allogeneic, “ready-to-use” macrophage-based therapy for platinum-resistant ovarian cancer. This is a ground-breaking, first-in-class therapy that shows very high efficacy in multiple solid tumors of unmet medical need.
Mechanism of Action
These cells are equipped with targeted therapy drugs complexed with the carrier protein, ensuring their stability in the carrier cell. The protein-drug complex is transferred specifically to cancer cells. The whole concept of this cell therapy is based on the groundbreaking scientific discoveries of MDC (Macrophage-Drug Conjugate).
Research Grants and Recognition
Two European Research Council (ERC) grants were received to study the molecular basis of the discovered mechanism in 2016 and 2020. In 2018, this project was selected to be promoted as one of the 10 European projects during the ERC 10th Anniversary.
Project Goals
The MACOV project will generate a complete efficacy data package for the pre-clinical development of the MDC-735 product, which includes:
- Efficacy in multiple animal models for platinum-resistant ovarian cancer
- Pharmacokinetics (PK)
- Pharmacodynamics (PD)
- Toxicology study
- Consolidation of intellectual property (IP)
- Validation of the business case
Expected Outcomes
The result of the project will be a validated cell therapy product for platinum-refractory ovarian cancer, tested for effectiveness and ready-to-use for the Phase I clinical trial.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 2.499.998 |
Totale projectbegroting | € 2.499.998 |
Tijdlijn
Startdatum | 1-11-2022 |
Einddatum | 31-10-2025 |
Subsidiejaar | 2022 |
Partners & Locaties
Projectpartners
- CELLIS SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIApenvoerder
Land(en)
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