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Efficacy, Safety and Tolerability of AFQ056 in Fragile X Patients

Fragile X Syndrome Clinical Trial

Official title:
A Multi-centre, Randomized, Double-blind, Placebo Controlled, Two-period, Crossover Proof-of-concept Study in Male Patients With Fragile X Syndrome to Assess the Efficacy, Safety and Tolerability of Multiple Oral Doses of AFQ056

Clinical Trial Summary

This study will evaluate the safety, tolerability and efficacy of multiple doses of AFQ056 in patients with Fragile X Syndrome. The dose range will be 50 to 150 mg b.i.d. The primary read-out of efficacy is reduction in Aberrant-Behavior Checklist score.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00718341
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 2
Start date June 2008
View Details
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