Opportunity Overview
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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Start FreeSolicitation Details
| Issuing agency | MRC |
|---|---|
| Country | United Kingdom |
| Category | Research Development |
| Published | September 30, 2022 |
| Procurement stage | Active solicitation |
| Response due | September 29, 2026 |
| Status | Open — accepting responses |
| Official source | View original notice |
| Last verified | August 12, 2026 |
Source: UK Research and Innovation (UKRI) — Open Government Licence v3.0.
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