Harness Therapeutics nominates HRN001 for Huntington’s disease
HRN001 is a first-in-class antisense oligonucleotide upregulating FAN1. The company forms a Clinical Advisory Board to guide clinical progression in 2027.
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Biotechnology company developing precision therapies for neurodegenerative diseases
harnesstx.comLast updated
In short: Harness Therapeutics nominated HRN001 for Huntington’s, launched MISBA Duo, and won an MJFF Parkinson’s grant.
HRN001 is a first-in-class antisense oligonucleotide upregulating FAN1. The company forms a Clinical Advisory Board to guide clinical progression in 2027.
She brings over 20 years of biopharma experience, including fundraising, partnerships, and leadership roles at Samsara Therapeutics and others. Her expertise supports growth in neurodegenerative therapeutics.
The platform enables simultaneous upregulation and downregulation of two targets. It collaborates with Ono Venture Investment on an R&D program for a rare triplet repeat disorder.
The SAB includes leaders in genetics, biology, and Huntington’s disease to guide HRN001 development and pipeline expansion. CTA-enabling studies for HRN001 start in 2025.
Dr Andy Billinton, CSO will present preclinical data at the upcoming CHDI Foundation Huntington’s Disease Therapeutics Conference · Cambridge, UK, 16 February 2026: Harness Therapeutics...
R&D programme with Ono Venture Investment builds on insights from first generation platform, and targets an undisclosed rare triplet repeat disorder Cambridge, UK, 06 October...
(MENAFN- GlobeNewsWire - Nasdaq) Dr Paulo Fontoura brings 20 years' experience of working in the pharma industry, with the most recent 16 years focusing on...
Cambridge, UK, April 24 2024: Harness Therapeutics, a biotechnology company focused on protein upregulation to develop next generation therapeutics for neurodegenerative diseases, today announced the...
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