A combined diagnostic and targeted gene therapy platform for brain tumor relapse
This project aims to develop a novel gene therapy using engineered viruses to target therapy-resistant brain tumor cells, improving patient prognosis and treatment outcomes.
Projectdetails
Introduction
Emergence of therapy resistance is a major cause of death following conventional chemotherapy and radiation for children and adults with malignant brain tumors. It is imperative to find novel options to target therapy-resistant brain tumor populations to save lives. We propose a novel platform providing a prognostic tool and a suicide gene therapy tool using engineered viruses.
Proposed Strategy
It involves targeting freshly biopsied cells from brain tumor patients with our strategy in combination with standard therapy to predict the risk of patients developing relapse and a gene therapy suicide tool to remove cells causing relapse.
Novel Approach
Previous suicide gene therapies have only used viruses hitting dividing tumor cells. Our strategy will use an engineered virus targeting non-dividing tumor cells that we know escape standard therapy.
- After removing the tumor bulk using standard treatment, we propose to use our virus with a marker for diagnostic purposes.
- Alternatively, we will use a suicide gene that will be activated by a prodrug to eradicate therapy-resistant cells.
Prodrug administration before recurrence will eliminate relapsed cells once they start dividing and become dangerous.
Impact of the Strategy
The impact of our strategy will be high, providing health care professionals with a better tool to identify patients at high risk of developing recurrence. Such patients can receive a better, more tailored treatment that will not only increase their chance of survival but also reduce their time under hospital care and rehabilitation.
Intellectual Property and Market Analysis
We protected our strategy with a filed patent and assessed our regulatory needs. We completed a market analysis to evaluate market size and potential benefit for cancer patients.
Competitors and Collaborators
We have disclosed competitors but also potential collaborators that can co-finance and move our strategy forward to in vitro diagnostic device registration and initial clinical trials.
Funding Proposal
In our proposal, we will apply for funding covering lab work to test efficacy and safety, help with registration, and negotiation strategies.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 150.000 |
Totale projectbegroting | € 150.000 |
Tijdlijn
Startdatum | 1-9-2022 |
Einddatum | 29-2-2024 |
Subsidiejaar | 2022 |
Partners & Locaties
Projectpartners
- UPPSALA UNIVERSITETpenvoerder
- UPPSALA UNIVERSITET RESEARCHINTELLECTUAL PROPERTY AB
Land(en)
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Voorkomen van therapieresistentie bij kanker
Dit project onderzoekt een bloedgebaseerde methode voor vroege detectie van therapieresistentie bij kanker om levensverwachting te verbeteren.
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This project aims to develop a high-throughput protocol for producing gene-corrected CAR T cells and blood stem cells using optimized photoporation and CRISPR technology for enhanced clinical application.
Development of innovative proton and neutron therapies with high cancer specificity by 'hijacking' the intracellular chemistry of haem biosynthesis.
NuCapCure aims to develop novel cancer treatments for glioblastoma by utilizing custom-made drugs through biosynthesis to enhance proton and neutron therapies for better targeting and efficacy.
TraffikGene-Tx: Targeted Peptide Carriers for RNA Delivery
TraffikGene-Tx aims to develop safe, scalable peptide carriers for targeted RNA delivery, addressing genetic diseases and enhancing NAT therapies to improve patient outcomes and reduce healthcare costs.