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Clinical Trial Summary

The aim of this study is to utilize neurophysiologic assessments, behavioral measures and clinical measures to assess how much deficits associated with Fragile X Syndrome from pre-dose to post-dose using pharmacology.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05418049
Study type Interventional
Source Children's Hospital Medical Center, Cincinnati
Contact Hannah J. Sachs, MPA
Phone 513-636-2592
Email hannah.sachs@cchmc.org
Status Recruiting
Phase Phase 2
Start date September 8, 2022
Completion date June 30, 2025

See also
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