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Clinical Trial Summary

This is an open-label, multi-center study designed to extend the evaluation of the safety, tolerability, and clinical effects of oral administration of KNS-760704 in patients with ALS.


Clinical Trial Description

Patients who complete the Part 2 Week 28 visit in study KNS-760704-CL201 and patients with ALS who were actively receiving RTPB [(6R)-4,5,6,7-tetrahydro-N6-propyl-2,6-benzothiazolediamine dihydro-chloride monohydrate] under Research IND #60,948 were eligible to participate in this study. Eligible patients received 1 tablet of KNS-760704 (150 mg) every 12 hours (Q12H) (300 mg total daily dose) for up to 180 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00931944
Study type Interventional
Source Knopp Biosciences
Contact
Status Completed
Phase Phase 2
Start date July 2009
Completion date July 2013

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