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Press releaseGlobeNewswire· February 16, 2026

Harness Therapeutics Nominates HRN001, a First-in-Class Drug Candidate for Huntington’s Disease and Establishes Clinical Advisory Board

View original at globenewswire.com
Harness Therapeutics Nominates HRN001, a First-in-Class Drug Candidate for Huntington’s Disease and Establishes Clinical Advisory Board HRN001 is a potent and specific antisense oligonucleotide designed to drive controlled upregulation of FAN1, a genetically validated target in Huntington’s disease Clinical Advisory Bo…
Opening lines of the source · GlobeNewswire · short snapshot — read the full document at the original

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  • There are currently no approved disease-modifying treatments available for Huntington's disease.

    80% confidence
  • Harness is exploring the potential of the MISBA® platform in other triplet repeat disorders and across a broader pipeline of neurodegenerative disorders.

    80% confidence
  • FAN1 nuclease has emerged as one of the most compelling targets to suppress somatic expansion, demonstrating the strongest genetic association to disease onset in genome-wide association studies.

    80% confidence
  • HD is caused by the expansion of CAG repeats in the huntingtin (HTT) gene. Ongoing somatic expansion of these repeats is now recognised as a key driver of disease onset and progression.

    80% confidence
  • HRN001 has demonstrated robust upregulation of FAN1 and slowing of somatic expansion in models of HD, as well as favourable PK and tolerability characteristics.

    80% confidence
  • The nomination of HRN001 represents a pivotal milestone for Harness and underscores commitment to the Huntington's disease community. HRN001 represents a differentiated, first-in-class therapeutic approach for addressing somatic expansion.

    80% confidence
  • FAN1 is one of the most compelling and consistently validated genetic modifiers of Huntington's disease identified to date, with a clear mechanistic link to somatic expansion and disease progression. Harness' approach with HRN001 offers a novel and highly targeted way to therapeutically modulate this pathway.

    80% confidence
  • HD leads to progressive cognitive, psychiatric and motor decline, with death often occurring within 15 years of symptom onset.

    80% confidence

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