CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 51 enrolled
Drug / intervention
GSK2402968 3mg/kg/week +3 moredrug
Likely dose
GSK2402968 3mg/kg/weekfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01462292
NCT01462292Phase 2Completed

An Exploratory Study to Assess Two Doses of GSK2402968 in the Treatment of Ambulant Boys With Duchenne Muscular Dystrophy

GlaxoSmithKline·interventional·Posted Oct 31, 2011·Updated Oct 16, 2017

In Brief

A Phase 2 clinical trial evaluating GSK2402968 3mg/kg/week, GSK2402968 6 mg/kg/week, and 2 other interventions for Muscular Dystrophies. Completed, enrolled 51 participants across 14 sites.

Detailed Summary

The purpose of this study is to determine if GSK2402968 is effective in the treatment of ambulant boys with Duchenne muscular dystrophy resulting from a mutation thought to be corrected by exon 51 skipping. Two doses of GSK2402968 and placebo will be used in this study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedOct 31, 2011
Enrollment StartOct 26, 2011
Primary CompletionMay 21, 2013
Study CompletionNov 4, 2013
TodayJul 2, 2026
Enrollment to primary: 1.6 yearsPosted 14.7 years ago

Interventions

GSK2402968 3mg/kg/weekdrug

Comparison of 2 doses of GSK2402968

GSK2402968 6 mg/kg/weekdrug

Comparison of 2 doses of GSK2402968

Placebo to match GSK2402968 3 mg/kg/weekdrug

Matched placebo

Placebo to match GSK2402968 6 mg/kg/weekdrug

Matched Placebo