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001     798313
005     20230215042541.0
024 7 _ |a G:(EU-Grant)864121
|d 864121
|2 CORDIS
024 7 _ |a G:(EU-Call)ERC-2019-COG
|d ERC-2019-COG
|2 CORDIS
024 7 _ |a corda__h2020::864121
|2 originalID
035 _ _ |a G:(EU-Grant)864121
150 _ _ |a Macro-Nanomedicine to Treat Metastatic Cancer
|y 2020-04-01 - 2025-03-31
371 _ _ |a Universitätsklinikum Aachen
|b UKA
|d Germany
|e http://www.ukaachen.de/
|v CORDIS
372 _ _ |a ERC-2019-COG
|s 2020-04-01
|t 2025-03-31
450 _ _ |a Meta-Targeting
|w d
|y 2020-04-01 - 2025-03-31
510 1 _ |0 I:(DE-588b)5098525-5
|a European Union
|2 CORDIS
680 _ _ |a Metastatic cancer is a complex and highly heterogenous disease, which is very difficult to treat. The aim of the Meta-Targeting project is to establish a holistic, rational and realistic nanomedicine-based approach to improve the treatment of metastatic breast cancer. Concrete objectives are: (1) the development of polymeric micelles which can be efficiently and stably co-loaded with three different drugs and with an imaging agent; (2) the use of physical and pharmacological means to modulate the vasculature and microenvironment in tumors and metastases; (3) the identification of imaging- and biopsy-based biomarkers for patient selection; (4) the incorporation of drugs to overcome cellular and microenvironmental multidrug resistance; and (5) the implementation of multifunctional micelles to enhance the efficacy of immunotherapy. It is envisaged that micelles loaded with in-house developed doxorubicin prodrugs are able to induce immunogenic cell death in tumors and metastases without causing systemic immunodepression, that co-loading with the angiotensin receptor inhibitor losartan helps to prime tumors and metastases for improved delivery (of micelles, immunomodulatory antibodies and T cells), and that co-loading with the P-glycoprotein inhibitor tariquidar assists in inducing immunogenic cell death, while avoiding typical anti-Pgp side effects, such as neurotoxicity. Physical priming with ultrasound and microbubbles will promote the delivery of micelles, antibodies and T cells to and into primary tumors. Imaging- and biopsy-based biomarkers are needed to allow for patient stratification, which is critically important to improve the clinical translation of cancer nanomedicines. The outcomes of the different project lines in Meta-Targeting will - alone and especially together - be truly transformative: they will contribute to scientific and clinical progress in nanomedicine, in tumor-targeted drug delivery, in immunotherapy, and in the treatment of metastatic cancer.
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980 _ _ |a CORDIS
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