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Clinical Trial Summary

This is a single dose, placebo-controlled study. Male subjects aged 18 to 40 years (inclusive) with a diagnosis of FXS. Eligible subjects may enroll in this study comprised of two in home and two in clinic visits each 14 days apart, for a total of four visits. Subjects will be given single dose gaboxadol (10 mg) or matched placebo at each of these visits to take orally. Thus, all enrolled subjects will receive placebo at home and in clinic and receive gaboxadol at home and in clinic in a blinded fashion.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06334419
Study type Interventional
Source Children's Hospital Medical Center, Cincinnati
Contact Ashley Dapore
Phone 513-517-1580
Email ashley.dapore@cchmc.org
Status Recruiting
Phase Phase 2
Start date January 29, 2024
Completion date September 30, 2024

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