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Clinical Trial Summary

This is an open label, off label study, to provide interested ALS patients with Ciprofloxacin/Celecoxib fixed dose combination, while assessing safety and tolerability, routine disease progression measures (ALSFRS-R and Vital Capacity).


Clinical Trial Description

Patients will be prescribed a fixed dose combination of Ciprofloxacin and Celecoxib to be taken twice daily, and will be monitored for safety and tolerability. Additionally, routine progression measures will be assessed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04090684
Study type Interventional
Source NeuroSense Therapeutics Ltd.
Contact
Status Completed
Phase Phase 1
Start date December 9, 2019
Completion date January 20, 2022

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