drugset / Trial / NCT01494701

An Open-label Safety, Tolerability, and Dose-range Finding Study of Nusinersen (ISIS 396443) in Participants With Spinal Muscular Atrophy (SMA)

NCT01494701

Phase 1 Completed 28 enrolled Biogen
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This objectives of this study are to evaluate the safety, tolerability, and pharmacokinetics of a single dose of nusinersen (ISIS 396443) administered intrathecally to participants with Spinal Muscular Atrophy (SMA).

Timeline

Start
2011-11-30
Primary completion
2013-01-31
Completion
2013-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Nusinersen Antisense oligonucleotide Intrathecal