A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study of NIDO-361 in Patients With Spinal and Bulbar Muscular Atrophy (SBMA)
Latest Information Update: 29 Oct 2024
At a glance
- Drugs NIDO-361 (Primary)
- Indications X-linked bulbo-spinal atrophy
- Focus Adverse reactions; Therapeutic Use
- Acronyms PIONEER KD
- Sponsors Nido Biosciences
Most Recent Events
- 26 Oct 2024 Planned End Date changed from 1 Aug 2025 to 1 Oct 2025.
- 26 Oct 2024 Planned primary completion date changed from 1 Aug 2025 to 1 Oct 2025.
- 22 Oct 2024 According to a Nido Biosciences media release, European Medicines Agency (EMA) has granted Orphan Drug Designation to their lead clinical candidate NIDO-361, for the treatment of Spinal and Bulbar Muscular Atrophy (SBMA), this designation is awarded as the company has completed enrollment for a phase 2 study of the drug.