A study of the efficacy and safety of RO4917523 in patients with Fragile X Syndrome

Registry ID
EUCTR2011-004349-42
Source registry
EUCTR
Status
Completed
Phase
PHASE2
Sponsor
F. Hoffmann-La Roche Ltd.
Start date
2012-05-23
Completion date
2014-04-04
Last update
2026-08-16

Conditions

Summary

• To evaluate the efficacy of 12-week treatment with RO4917523 in patients with Fragile X Syndrome (FXS) as measured by the ADAMS total score • To evaluate the safety and tolerability of 12-week treatment with RO4917523 in patients with FXS

Locations

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