Extension Study Evaluating The Safety And Tolerability of AMX0035

Status Enrolling by invitation

Clinical Trial Summary

The primary objective is to evaluate the safety and tolerability of AMX0035 over 108 weeks of open label treatment for participants previously enrolled in Study A35-004 (PHOENIX).

Clinical Trial Description

All participants will receive open-label treatment with AMX0035, starting on Day 1 with twice a day oral dosing (once in the morning and once in the evening) for the duration of the study. After the Baseline Visit (Day 1), enrolled participants will complete visits approximately every 12 weeks (± 2 weeks), until Week 108 or the end of treatment (EOT) visit, followed by a safety follow-up approximately 28 days after the last dose. A survival follow-up assessment will be completed every 12 weeks following the EOT visit until time of death or end of study (EOS). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05619783
Study type	Interventional
Source	Amylyx Pharmaceuticals Inc.
Contact
Status	Enrolling by invitation
Phase	Phase 3
Start date	December 29, 2022
Completion date	August 2026

View Details

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