drugset / Trial / NCT06914609

REVEAL: A Phase 3 Study of ION582 in Angelman Syndrome

NCT06914609 ↗

Phase 3 Recruiting 158 enrolled Ionis Pharmaceuticals, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of ION582 in children and adults with Angelman syndrome caused by a deletion or mutation of the UBE3A gene.

Timeline

Start
2025-06-10
Primary completion
2027-08
Completion
2030-04

Drugs

EvaluationDrugModalityDoseRoute
Subject OBUDANERSEN SODIUM Unknown 40 mg Intrathecal
Subject OBUDANERSEN SODIUM Unknown 80 mg Intrathecal

Indications