
Shares of Sarepta Therapeutics SRPT.O 3% at $20.92 premarket
Drugmaker says it received approval in New Zealand to begin first human study of SRP‑1005 for Huntington's disease, a rare fatal brain disorder
Co's SRP‑1005 is an experimental treatment designed to target the genetic cause of the condition - SRPT
Early‑stage trial to enroll about 24 participants and focus on safety and tolerability; study expected to start in Q2 2026, per co
Huntington's disease is a rare inherited disorder that damages nerve cells in the brain, causing worsening movement and thinking problems
Shares down ~82% in 2025