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ANAVEX2-73 Study in Patients With Rett Syndrome — AVATAR  

Rett Syndrome Clinical Trial

Official title:
A Double-Blind, Randomized, Placebo-Controlled, Safety and Efficacy Study of ANAVEX2-73 in Patients With Rett Syndrome

Clinical Trial Summary

ANAVEX2-73-RS-002 is a Phase 3, double-blind, randomized, placebo-controlled dose escalation safety, tolerability and efficacy study in patients 18 years and older with RTT using endpoints including multiple clinical and exploratory molecular and biochemical measures.

Clinical Trial Description

This Phase 3 safety, tolerability and efficacy study is designed as a double-blind, randomized, placebo-controlled study. This is a 7-week placebo-controlled study of ANAVEX2-73 oral solution for the treatment of patients with RTT 18 years or older. A voluntary option will be offered for all patients to continue a 48-week open label extension. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03941444
Study type Interventional
Source Anavex Life Sciences Corp.
Contact
Status Completed
Phase Phase 3
Start date May 6, 2019
Completion date September 30, 2021
View Details
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