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Clinical Trial Summary

This is an OLE study conducted to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and clinical effects of WVE-004 in adult patients with ALS, FTD, or mixed ALS/FTD phenotype with a documented mutation in the C9orf72 gene. To participate in the study, patients must have successfully completed Phase 1b/2a WVE-004-001 study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05683860
Study type Interventional
Source Wave Life Sciences Ltd.
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date December 14, 2022
Completion date June 30, 2023

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