Biomarker and DNA Collection in Subjects Participating in Protocol 22003

Completed

Conditions studied: Fragile X Syndrome

In brief

The subjects that meet the inclusion and exclusion criteria and consent to participate in protocol 22003 will be offered participation in 22003A which will evaluate secreted protein before and after treatment with STX209 and placebo to determine if they correlate with effectiveness of treatment or susceptibility to treatment with STX209. These same subjects will also be asked to contribute a blood sample for DNA (deoxyribonucleic acid) collection. The investigators will study the DNA to determine if STX209 works better in people with specific gene variations, or to find new gene variations that predict how well STX209 works.

Key facts

Study ID

NCT00892580

Run by

Seaside Therapeutics, Inc.

People needed

32

Starts

2009-05-01

Last updated by the study team

2013-07-31

Who can join

Age: 6 and older, up to 17. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• The Autism Spectrum Disorder subjects that meet the inclusion and exclusion criteria and consent to participate in protocol 22003

You may not qualify if…

• The Autism Spectrum Disorder subjects that meet the inclusion and exclusion criteria and consent to participate in protocol 22003

Where it is running

• Southwest Autism Research & Resource Center — Phoenix, Arizona, United States
• University of California-Los Angeles Neuropsychiatric Institute — Los Angeles, California, United States
• Yale Child Study Center — New Haven, Connecticut, United States
• Riley Hospital for Children — Indianapolis, Indiana, United States
• University of North Carolina Neurosciences Hospital — Chapel Hill, North Carolina, United States
• Vanderbilt Kennedy Center — Nashville, Tennessee, United States
• Red Oaks Psychiatry Associates, PA — Houston, Texas, United States
• Seattle Children's Hospital — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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