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Safety, Tolerability and Efficacy of the Transdermal System in Elderly Subjects With Major Depression

Major Depression Clinical Trial

Official title:
A Phase III, Open-Label Study of the Safety, Tolerability and Efficacy of the Selegiline Transdermal System in Elderly Subjects With Major Depression

Clinical Trial Summary

Objective of this 16-week, open-label study is to assess the safety and tolerability of once daily application of three doses of STS during continuous dosing in the treatment of elderly subjects with major depression. Subjects will have study visits (clinic visits) at beginning of study (baseline) and study weeks 1, 3, 5, 8, 12, and 16.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00285766
Study type Interventional
Source Somerset Pharmaceuticals
Contact
Status Completed
Phase Phase 3
Start date August 2002
Completion date July 2005
View Details
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