OLIGOMED | Oligonucleotides for Medical Applications

Summary
The use of synthetic oligonucleotides (ONs, short DNA or RNA strands) in the treatment of genetic diseases is a rapidly growing field, and the most promising alternative to gene therapy or small molecules. Most pharmaceutical companies shift from in-house platform development to product-specific licensing and co-development to get ON based therapies past clinical trials. Therefore there is a growing and currently unmet need for a combined academic and industry-based multidisciplinary research to further advance the field by bringing together the separated and fragmented R&D efforts of diverse ON technologies.

OLIGOMED will address these needs by:
- uniting world-class academic and private sector expertise in ON chemistry, bio-analysis and medical applications
- developing a next generation ON platform technology based on combining tailored synthetic ONs with smart delivery
- optimising ON therapies through testing in medicinal environments

We will use these novel ON technologies to develop innovative treatment options for high-impact genetic diseases, i.e. Huntington’s disease, cardiovascular diseases and cancer.

Our European intersectoral and multidisciplinary research and training network for 15 Early Stage Researchers (ESRs) will deliver:
-highly skilled scientific staff required to fully exploit ON therapeutics for personalised medicine
-top-class training in organic and chemoenzymatic synthesis, ON analysis, and biomedical/medicinal testing
-transferable skills courses, specific industry relevant workshops and public engagement activities

This combination makes OLIGOMED a truly exciting programme for ESRs. The platform will immediately benefit to both European citizens and commercial partners. In the long term, OLIGOMED`s flexible platform technology will be taken forward by our private sector and research institutions for exploitation and will thus strengthen the European innovation capacity in the field of ON therapies.
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More information & hyperlinks
Web resources: https://cordis.europa.eu/project/id/956070
Start date: 01-01-2021
End date: 30-06-2025
Total budget - Public funding: 4 130 663,40 Euro - 4 130 663,00 Euro
Cordis data

Original description

The use of synthetic oligonucleotides (ONs, short DNA or RNA strands) in the treatment of genetic diseases is a rapidly growing field, and the most promising alternative to gene therapy or small molecules. Most pharmaceutical companies shift from in-house platform development to product-specific licensing and co-development to get ON based therapies past clinical trials. Therefore there is a growing and currently unmet need for a combined academic and industry-based multidisciplinary research to further advance the field by bringing together the separated and fragmented R&D efforts of diverse ON technologies.

OLIGOMED will address these needs by:
- uniting world-class academic and private sector expertise in ON chemistry, bio-analysis and medical applications
- developing a next generation ON platform technology based on combining tailored synthetic ONs with smart delivery
- optimising ON therapies through testing in medicinal environments

We will use these novel ON technologies to develop innovative treatment options for high-impact genetic diseases, i.e. Huntington’s disease, cardiovascular diseases and cancer.

Our European intersectoral and multidisciplinary research and training network for 15 Early Stage Researchers (ESRs) will deliver:
-highly skilled scientific staff required to fully exploit ON therapeutics for personalised medicine
-top-class training in organic and chemoenzymatic synthesis, ON analysis, and biomedical/medicinal testing
-transferable skills courses, specific industry relevant workshops and public engagement activities

This combination makes OLIGOMED a truly exciting programme for ESRs. The platform will immediately benefit to both European citizens and commercial partners. In the long term, OLIGOMED`s flexible platform technology will be taken forward by our private sector and research institutions for exploitation and will thus strengthen the European innovation capacity in the field of ON therapies.

Status

SIGNED

Call topic

MSCA-ITN-2020

Update Date

28-04-2024
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Horizon 2020
H2020-EU.1. EXCELLENT SCIENCE
H2020-EU.1.3. EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions (MSCA)
H2020-EU.1.3.1. Fostering new skills by means of excellent initial training of researchers
H2020-MSCA-ITN-2020
MSCA-ITN-2020