Safety and Efficacy of an Anti-Psychotic in Patients With Schizophrenia
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|ClinicalTrials.gov Identifier: NCT00074477|
Recruitment Status : Completed
First Posted : December 15, 2003
Last Update Posted : May 24, 2011
|Condition or disease||Intervention/treatment||Phase|
|Schizophrenia||Drug: R092670||Phase 2|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||250 participants|
|Intervention Model:||Parallel Assignment|
|Official Title:||A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of 50 and 100 Mg-eq of Paliperidone Palmitate in Patients With Schizophrenia|
|Study Start Date :||October 2003|
|Study Completion Date :||July 2004|
- The change in total PANSS score from the start of the double-blind treatment period to the end of the double-blind treatment period.
- Changes from the start of to the end of the double-blind treatment period in CGI-S and in the PANSS subscales for specific symptoms. Incidence of adverse events, labs and ECGs throughout study.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00074477
|Study Director:||Johnson & Johnson Pharmaceutical Research & Development, L.L. C. Clinical Trial||Johnson & Johnson Pharmaceutical Research & Development, L.L.C.|