Oligonucleotide Therapy for Spinal and Bulbar Muscular Atrophy @UniversityHospitals
Oligonucleotide Therapy for Spinal and Bulbar Muscular Atrophy  @UniversityHospitals
Uploaded April 2026 | Updated September 2026, 1 week ago
Carlo Rinaldi, MA, MD, PhD, University of Oxford, 2024 Oxford-Harrington Rare Disease Scholar, is developing a splice-switching oligonucleotide therapy to target mutant androgen receptor in spinal and bulbar muscular atrophy, aiming to slow disease progression and improve quality of life for affected patients. The Oxford-Harrington Rare Disease Centre is a transatlantic initiative dedicated to accelerating breakthrough treatments and cures for rare diseases. Learn more: OxfordHarrington.org.
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Oligonucleotide Therapy for Spinal and Bulbar Muscular Atrophy

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