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ANAVEX2-73 Study in Pediatric Patients With Rett Syndrome — EXCELLENCE  

Rett Syndrome Clinical Trial

Official title:
ANAVEX2-73-RS-003 is a Phase 2/3, Double-blind, Randomized, Placebo-controlled Safety and Efficacy Study in Pediatric Patients With RTT

Clinical Trial Summary

ANAVEX2-73-RS-003 is a Phase 2/3, double-blind, randomized, placebo-controlled dose escalation safety, tolerability and efficacy study in patients 5-17 years of age with RTT using endpoints including multiple clinical and exploratory molecular and biochemical measures.

Clinical Trial Description

This Phase 2/3 efficacy study is designed as a double-blind, randomized, placebo-controlled study. This is a 12-week placebo-controlled study of ANAVEX2-73 oral solution for the treatment of patients with RTT 5-17 years of age. A voluntary option will be offered for all patients who meet the exposure criteria for ANAVEX2-73 to continue a 48-week open label extension. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04304482
Study type Interventional
Source Anavex Life Sciences Corp.
Contact
Status Completed
Phase Phase 2/Phase 3
Start date July 1, 2020
Completion date June 30, 2023
View Details
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