Characterising the biology of neurofilament light protein as a translational biomarker for Huntington's disease

MRC · United Kingdom government procurement

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September 29, 2026
Response Due
Active
Status

Opportunity Overview

Huntington's disease (HD) is a fatal neurodegenerative disorder characterized by a multitude of severe motor, cognitive, and psychiatric symptoms. It is caused by the inheritance of an expanded CAG repeat in the huntingtin gene1. Symptoms typically manifest between the ages of 30 and 50 years old, with underlying pathological changes occurring decades prior to onset2. These landmarks have been utilized alongside later cognitive, motor and functional markers to develop the HD Integrated Staging System (HD-ISS), a framework for characterising mutant huntingtin (mHTT) gene carriers for clinical trials and research purposes3.

Whilst there are currently no disease-modifying therapies available, numerous potential drug candidates exist within the developmental pipeline. However, the success of these potential treatments may be limited by the absence of biological tools to sensitively measure clinical benefit across short time periods. Prior to clinical manifestation, disease progression in HD is marked solely by MRI measurements of brain atrophy within the caudate and putamen of the basal ganglia3. Accurate measurement of potential therapeutic efficacy is challenging due to the slow rate of brain atrophy, the posited irreversible nature of brain loss in the earliest phases of the disease, and the small trial sample size in rare diseases such as HD. Moreover, atrophy is thought to be preceded by pathological changes at the molecular level4. The validation of an accessible, sensitive molecular biomarker would prove extremely useful both as a means of enriching the HD-ISS to add granularity to the early premanifest stages, and as a potential surrogate endpoint for future disease modifying clinical trials. Neurofilament light (NfL) has emerged as a promising candidate for this; it serves as an indicator of neuronal damage, measurable in both CSF and blood, and is significantly correlated with multiple clinical severity scores in HD5. Moreover, NfL levels in CSF have been...

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Solicitation Details

Issuing agencyMRC
CountryUnited Kingdom
CategoryResearch Development
PublishedSeptember 30, 2022
Procurement stageActive solicitation
Response dueSeptember 29, 2026
StatusOpen — accepting responses
Official sourceView original notice
Last verifiedAugust 12, 2026

Source: UK Research and Innovation (UKRI) — Open Government Licence v3.0.

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