Study Evaluating Desvenlafaxine Succinate Sustained-Release Tablets (DVS SR) In The Treatment Of Child and Adolescent Outpatients With Major Depressive Disorder

Completed · Phase 2

Conditions studied: Depressive Disorder, Major Depressive Disorder

In brief

The primary purpose of this study is to evaluate the long-term safety and tolerability of Desvenlafaxine Succinate Sustained-Release (DVS SR) in child and adolescent outpatients with major depressive disorder. A secondary aim is to evaluate the efficacy of DVS SR in the treatment of child and adolescent outpatients with major depressive disorder in an exploratory manner.

Key facts

Study ID

NCT00669110

Run by

Wyeth is now a wholly owned subsidiary of Pfizer

People needed

40

Starts

2008-05-01

Expected to finish

2010-05-01

Last updated by the study team

2021-08-19

Who can join

Age: 7 and older, up to 18. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Outpatients who have completed 8-weeks of treatment in the preceding study, 3151A6-2000, and who, in the opinion of the investigator, would benefit from long-term treatment.
• Study participants who are not surgically sterile or postmenopausal must agree and commit to the use of a reliable method of birth control for the duration of the study and for 15 days after the last dose of test article. Sexually active study participants must agree and commit to the use of condoms in addition to other contraceptive methods.

You may not qualify if…

• Clinically important abnormalities on baseline physical examination or any clinically significant abnormality on electrocardiogram (ECG), laboratory test results, or vital signs recorded before the final study day (day 56 visit) of the preceding study 3151A6-2000.
• Unresolved clinically significant adverse events or serious adverse events in the preceding study 3151A6-2000.
• Poor compliance with the preceding study 3151A6-2000, as assessed by the investigator and the medical monitor.
• Other exclusion criteria apply.

Where it is running

• Pfizer Investigational Site — Little Rock, Arkansas, United States
• Pfizer Investigational Site — North Miami, Florida, United States
• Pfizer Investigational Site — Terre Haute, Indiana, United States
• Pfizer Investigational Site — Wichita, Kansas, United States
• Pfizer Investigational Site — New Orleans, Louisiana, United States
• Pfizer Investigational Site — New York, New York, United States
• Pfizer Investigational Site — Cleveland, Ohio, United States
• Pfizer Investigational Site — Hershey, Pennsylvania, United States
• Pfizer Investigational Site — Houston, Texas, United States

Full record on ClinicalTrials.gov

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