Pridopidine in Amyotrophic Lateral Sclerosis (EAP 2)

Status Available

Clinical Trial Summary

This EAP will provide access to pridopidine for up to 200 patients with ALS who are ineligible for clinical trials. Pridopidine will be given at a dose of 45 mg twice daily p.o. (or via feeding tube). Each patient will be followed for 2 years with regularly scheduled visits. The screening and baseline visits will be performed in person; subsequent visits may occur in person or remotely. Recommended in-person visits will occur at Weeks 12, 52, 78, and end of treatment (Week 104 or early termination). If the patient is unable to complete the visits in person, these visits may also be completed remotely.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06069934
Study type	Expanded Access
Source	Prilenia
Contact	Victoria Wang
Phone	+1-857-282
Email	vjwang@mgh.harvard.edu
Status	Available
Phase

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