Open Label Study Investigating Safety and Efficacy of NPL2009 50 mg - 150 mg on Prepulse Inhibition Tests and Continuous Performance Tasks, Adults With Fragile X Syndrome
This study has been completed.
Sponsor:
Neuropharm
Information provided by (Responsible Party):
Neuropharm
ClinicalTrials.gov Identifier:
NCT00637221
First received: March 3, 2008
Last updated: April 26, 2012
Last verified: April 2012
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No Study Results Posted on ClinicalTrials.gov for this Study
| Study Status: | This study has been completed. |
|---|---|
| Study Completion Date: | April 2008 |
| Primary Completion Date: | April 2008 (Final data collection date for primary outcome measure) |