drugset / Trial / NCT01942590

Safety and Efficacy of Clenbuterol in Individuals With Late-onset Pompe Disease and Receiving Enzyme Replacement Therapy

NCT01942590

Phase 1/2 Completed 17 enrolled Dwight Koeberl, M.D., Ph.D.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Funding Source- FDA OOPD The purpose of this study is to investigate the safety and efficacy of clenbuterol on motor function in individuals with late-onset Pompe disease (LOPD) who are treated with enzyme replacement therapy (ERT).

Timeline

Start
2013-09
Primary completion
2016-09-02
Completion
2016-09-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Clenbuterol Small molecule 80 ug Oral