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Clinical trial

A 24-Week, Multicenter, Double-Blind, Randomized, Parallel-Group, Dose Ranging Study of the Efficacy and Safety of 3 Oral Doses of AVE1625 and Placebo on Top of Either Olanzapine, Risperidone/Paliperidone, Quetiapine or Aripiprazole in the Treatment of Cognitive Impairment in Schizophrenia.

NCT00439634 is registered in ClinicalTrials.gov with Sanofi as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A 24-Week, Multicenter, Double-Blind, Randomized, Parallel-Group, Dose Ranging Study of the Efficacy and Safety of 3 Oral Doses of AVE1625 and Placebo on Top of Either Olanzapine, Risperidone/Paliperidone, Quetiapine or Aripiprazole in the Treatment of Cognitive Impairment in Schizophrenia.
Lead sponsor
Sanofi
Phase
Phase 2
Overall status
Terminated
Start date
February 28, 2007
Completion date
September 30, 2009
Enrollment
873 (actual)
Sites
2

Conditions

As the registry lists them; a condition with its own page is linked.