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| Sponsored by: |
Johnson & Johnson Pharmaceutical Research & Development, L.L.C. |
| Information provided by: | Johnson & Johnson Pharmaceutical Research & Development, L.L.C. |
| ClinicalTrials.gov Identifier: | NCT00063297 |
Purpose
This study is to determine the efficacy (how well the drug works), safety, and side effects of the study medication compared to placebo in the treatment of the negative symptoms of schizophrenia in adults.
| Condition | Intervention | Phase |
|
Schizophrenia |
Drug: R209130 |
Phase II |
| MedlinePlus related topics: | Schizophrenia |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study |
Eligibility
| Ages Eligible for Study: | 18 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion:
Exclusion:
Contacts and Locations![]() |
Show 30 Study Locations |
| Johnson & Johnson Pharmaceutical Research & Development, L.L.C. |
More Information
| Study ID Numbers: | R209130-SCH-202 |
| First Received: | June 25, 2003 |
| Last Updated: | June 23, 2005 |
| ClinicalTrials.gov Identifier: | NCT00063297 |
| Health Authority: | United States: Food and Drug Administration |
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