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Completed Phase 3 Interventional

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

ClinicalTrials.gov ID: NCT00285766

Public ClinicalTrials.gov record NCT00285766. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 4, 2026, 3:55 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT00285766
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Somerset Pharmaceuticals
Industry
Enrollment
300 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
65 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2002
Primary completion
Not listed
Completion
Jun 30, 2005
Last update posted
Apr 21, 2008

2002 – 2005

United States locations

U.S. sites
15
U.S. states
7
U.S. cities
14
Facility City State ZIP Site status
Mohammed Bari, M.D. Chula Vista California 91910
Charles Meredith, M.D. San Diego California 92108
Daniel Zimbroff, M.D. Upland California 94589
Kathleen Toups, M.D. Walnut Creek California 94589
Abbey Strauss, M.D. Boynton Beach Florida 33437
Barry Baumel, M.D. Miami Beach Florida 33154
Margarita Nunez, M.D. St. Petersburg Florida 33702
Mildred Farmer, M.D. St. Petersburg Florida 33710
Larry Eisner, M.D. Tamarack Florida 33321
Andrew Cutler, M.D. Winter Park Florida 32789
Robert Riesenberg, M.D. Atlanta Georgia 30308
James Hartford, M.D. Florence Kentucky 41042
Mitchel Kling, M.D. Baltimore Maryland 21201
Louise Beckett, M.D. Oklahoma City Oklahoma 73103
Penny Barnhart, M.D. Wichita Falls Texas 76309

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00285766, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 21, 2008 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00285766 live on ClinicalTrials.gov.

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