PRodrug technology for Immunotherapy-priming via patient-friendly at-home MEtronomic dosing
The PRIME project aims to develop a novel prodrug platform for at-home metronomic dosing of chemotherapy to enhance immunotherapy efficacy in cancer treatment.
Projectdetails
Introduction
Immunotherapy holds great promise for curative cancer treatment. While immune checkpoint inhibitors can induce complete and long-term cures, the percentage of patients responding to immunotherapy remains low.
Combining Strategies
Combining immunotherapy with chemotherapeutic drugs that induce immunogenic cell death (ICD) is among the most promising strategies to potentiate antitumor immune responses.
Administration Challenges
Chemotherapeutics are typically administered via intravenous infusion, once every couple of weeks, at high doses. Metronomic dosing is based on the application of chemotherapy drugs at high frequency and low doses, and it is gaining increasing interest to potentiate chemo-immunotherapy responses.
However, high-frequency low-dose chemotherapy administration in the clinic via intravenous infusion is pragmatically undoable and economically not feasible.
Limitations of Current Methods
At-home administration via oral ingestion or subcutaneous self-injection is impossible because of the side effect spectrum of chemotherapeutic drugs.
Project Goals
In the PRIME project, we aim to establish PRodrug technology for Immunotherapy-priming via patient-friendly at-home MEtronomic dosing.
Prodrug Technology
Prodrugs have assisted in improving drug performance for over a century now, and they are widely employed in the pharmaceutical industry and clinical practice, with approximately 10% of new drug approvals technically being prodrugs.
Research Strategy
We will set out to establish a synthetic and formulation strategy to produce a novel immunogenic prodrug platform. Upon subcutaneous metronomic dosing, we will evaluate the preclinical performance of our prodrugs as monotherapy and in combination with immunotherapy in breast and prostate cancer mouse models.
Anticipated Outcomes
We anticipate that exploiting the technological and socio-economic potential of PRIME will unlock new avenues towards at-home cancer treatment opportunities with enhanced therapeutic outcomes and improved patient quality of life.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 150.000 |
Totale projectbegroting | € 150.000 |
Tijdlijn
Startdatum | 1-10-2023 |
Einddatum | 31-3-2025 |
Subsidiejaar | 2023 |
Partners & Locaties
Projectpartners
- UNIVERSITAETSKLINIKUM AACHENpenvoerder
Land(en)
Vergelijkbare projecten binnen European Research Council
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Modular Targeted Nanoplatform for Immune Cell Regulation and TherapyImmuNovation aims to develop a targeted nano-immunoModulator nanovaccine to enhance antitumor immunity against CEACAM5+ gastrointestinal cancers, offering a safer and more effective treatment alternative. | ERC Proof of... | € 150.000 | 2023 | Details |
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Live biotherapeutics to potentiate cancer immunotherapy
The project aims to enhance immunotherapy efficacy by using engineered live biotherapeutics to normalize tumor stiffness and improve blood flow in colorectal and breast cancer models.
Nano-assisted digitalizing of cancer phenotyping for immunotherapy
The ImmunoChip project aims to develop a microfluidic device that analyzes cancer-immunity interactions to predict patient responses to immunotherapy, enhancing treatment efficacy and outcomes.
Developing the next generation of cis-targeting macrophage-T cell cancer immunotherapies
This project aims to develop dual-modulatory agents to enhance anti-tumor immune responses in cancer immunotherapy while minimizing side effects, seeking proof-of-concept validation.
Modular Targeted Nanoplatform for Immune Cell Regulation and Therapy
ImmuNovation aims to develop a targeted nano-immunoModulator nanovaccine to enhance antitumor immunity against CEACAM5+ gastrointestinal cancers, offering a safer and more effective treatment alternative.
RNA-based cancer ImmunotheraPeutics to Enhance CROssPrimming
The RIPECROP project aims to enhance cancer immunotherapy by developing mRNA-based agents that boost cDC1 cells in tumors to improve anti-tumor T-cell crosspriming.
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Functional chemical reprogramming of cancer cells to induce antitumor immunity
The RESYNC consortium aims to revolutionize cancer immunotherapy by reprogramming cancer cells into antigen-presenting dendritic cells using small molecules for personalized and safer treatments.
Anticancer approach based on the Metabolic Disruption of Cancer Stem Cells with high effectivity across a wide range of solid tumours
The project aims to develop the novel anticancer agent IGN116, targeting cancer stem cells in CRC and PDAC, to provide effective treatment with low toxicity, benefiting thousands of patients by 2040.
Breakthrough Neoantigen-specific Tumor-Infiltrating Lymphocyte Therapies Through Novel Dendritic Cell Reprogramming
The Repro-TIL project aims to enhance tumor-reactive TIL expansion for more effective immunotherapy in solid tumors, paving the way for improved treatment outcomes and commercialization.
IOO: a novel assay to predict patient response to immune checkpoint inhibitors, optimising patient stratification to these therapies and tripling solid tumour patient outcomes in immuno-oncology.
The project aims to enhance cancer immunotherapy efficacy by developing a validated biomarker assay to predict patient responses, potentially doubling survival rates for lethal tumors.
Clinical readiness of a live biotherapeutic for treatment of Non-Small Cell Lung Cancer (NSCLC)
Pulmobiotics aims to develop PB_LC, an engineered Mycoplasma pneumoniae strain, to enhance immunotherapy for NSCLC patients by improving T cell infiltration and overcoming treatment resistance.