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Clinical Trial Summary

This study is designed to provide 6-months continuous dosing with the study medication, called HT-100, on participants who successfully completed the predecessor study (HALO-DMD-01). The main purpose of this study is to assess chronic safety, tolerability, pharmacodynamic activity (testing the drug's effect on DMD) and population pharmacokinetics (measuring how much drug is in the bloodstream) in participants with a broad spectrum of Duchenne muscular dystrophy (DMD).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01978366
Study type Interventional
Source Processa Pharmaceuticals
Contact
Status Terminated
Phase Phase 2
Start date October 2013
Completion date April 30, 2016

See also
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