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This study is designed to evaluate the efficacy and safety in Social Anxiety Disorder (SAD)
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| BRL29060A | Drug | |||
| paroxetine hydrochloride hydrate | Drug |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change from baseline in the LSAS total score at week 52 (Score at week 52- Score at week 0) | 52 Weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Proportion of patients responding with a CGI Global Improvement Item. Change from baseline in the CGI Severity of Illness score. Change from baseline in the HAM-D total score. Proportion of patients continuing treatment. | 52 Weeks |
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Inclusion criteria:
Exclusion criteria:
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| Name | Affiliation | Role |
|---|---|---|
| GSK Clinical Trials | GlaxoSmithKline | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| GSK Investigational Site | Saitama | 332-0012 | Japan | |||
| GSK Investigational Site |
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| ID | Term |
|---|---|
| D000072861 | Phobia, Social |
| D001008 | Anxiety Disorders |
| D004194 | Disease |
| ID | Term |
|---|---|
| D010698 | Phobic Disorders |
| D001523 | Mental Disorders |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| Tokyo |
| 194-0022 |
| Japan |
| GSK Investigational Site |