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NEXGEN-PD · Project

Next-Gen Skin-Based Vaccine and Early Diagnostic Tool for Parkinson's Disease

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Imagine your skin as a high-tech security gate that can be tricked into training your immune system more effectively. This project uses that trick to create a vaccine that clears out the toxic protein clumps causing Parkinson's. It also includes a simple blood-like test to catch the disease before the brain is permanently damaged.

By the numbers
8.5 million
individuals suffering from PD
12
consortium partners
The business problem

What needed solving

Parkinson's Disease lacks curative therapies and early diagnosis tools, leaving 8.5 million people with treatments that only manage symptoms without stopping disease progression.

The solution

What was built

A proprietary WISIT vaccine platform for aSyn targeting and an EV-based biomarker assay for early liquid biopsy diagnosis.

Audience

Who needs this

Vaccine manufacturersNeurological diagnostic labsBiopharmaceutical companiesPoint-of-care device developers
Business applications

Who can put this to work

Pharmaceuticals
mid-size
Target: Biotech vaccine developer

If you are a biotech vaccine developer dealing with low immune responses in traditional vaccines — this project developed the WISIT platform that uses skin dendritic cells to create stronger, more specific responses with fewer adjuvants.

Medical Diagnostics
SME
Target: Point-of-care testing provider

If you are a diagnostic provider dealing with the lack of early Parkinson's detection — this project developed an extracellular vesicle (EV)-based biomarker assay that enables early diagnosis via liquid biopsies.

Healthcare Services
enterprise
Target: Neurology clinic network

If you are a clinic network dealing with the high financial burdens of 8.5 million PD patients — this project developed a disease-modifying treatment and diagnostic tool to intervene before irreversible brain damage occurs.

Frequently asked

Quick answers

What is the estimated cost of the treatment?

Based on available project data, the objective is to achieve a 'cheap and effective' disease-modifying treatment, though specific price points are not listed.

Can this be produced at an industrial scale?

The project includes the manufacture of GMP-grade constructs, which is a requirement for industrial-scale pharmaceutical production.

Who owns the IP and how is it licensed?

The project utilizes the proprietary WISIT platform owned by the coordinator; however, specific licensing terms for the 12 partners are not provided in the dataset.

What is the timeline for market entry?

The project runs from 2023-04-01 to 2027-03-31, aiming to translate results into first-in-human Phase I/Ib clinical trials.

How does this integrate into current clinical workflows?

The EV-based biomarker assay is designed for liquid biopsies and is specifically intended to be suitable for point-of-care use.

Consortium

Who built it

The consortium is heavily industry-weighted with 8 industrial partners (67% ratio), 7 of which are SMEs. This strong commercial presence, spanning 6 countries (AT, DE, FR, HU, NL, UK), suggests a high focus on commercial translation and GMP manufacturing rather than purely academic research.

How to reach the team

Contact TRIDEM BIOSCIENCE GMBH & CO KG in Austria

Next steps

Talk to the team behind this work.

Contact us to explore licensing opportunities for the WISIT platform.

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