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Clinical Trial Summary

This is a prospective, open-label, follow up study to protocol 101/2 - continued treatment by IPL344 IV administered once a day in up to 15 participants with ALS. The study is designed to determine the safety, tolerability and initial efficacy of IPL344, administered once a day, by IV infusion for up to 36 months


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03755167
Study type Interventional
Source Immunity Pharma Ltd.
Contact
Status Suspended
Phase Phase 2
Start date December 9, 2018
Completion date February 2026

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