Overview

Safety, Tolerability and Efficacy Study of STX209 in Subjects With Fragile X Syndrome

Status:
Completed
Trial end date:
2010-05-01
Target enrollment:
Participant gender:
Summary
The study objective is to explore the efficacy, safety and tolerability of STX209 for treatment of irritability in subjects with FSX. We hypothesize that STX209 will improve irritability and other typical problem behaviors associated with fragile X syndrome. We also hypothesize that STX209 will be safe and well tolerated.
Phase:
Phase 2
Details
Lead Sponsor:
Seaside Therapeutics, Inc.