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Study Evaluating DVS-233 SR And Venlafaxine ER In Adult Outpatients With Major Depressive Disorder

Last updated on March 15, 2019

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Study Location
Contact
1-800-718-1021
Eligibility criteria
Condition
The disease, disorder, syndrome, illness, or injury that is being studied.
Major Depressive Disorder
Sex
Females and Males
Age
Pediatric Trials: 0-17 Years
Adult Trials: 18+ Years
18-75 years
Inclusion criteria
The factors, or reasons, that allow a person to participate in a clinical study.
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- Men and women 18 to 75 years of age, inclusive.

- Sexually active individuals participating in the study must use a medically acceptable
form of contraception during the study and for at least 15 days after the last dose of
test article

- Subjects must have a primary diagnosis of major depressive disorder

Exclusion criteria
The factors, or reasons, that prevent a person from participating in a clinical study.
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- Treatment with DVS-233 SR at any time in the past

- Treatment with venlafaxine (immediate release [IR] or extended release [ER]) within 90
days of study day 1

- Known hypersensitivity to venlafaxine (IR or ER)

NCT00090649
Pfizer
Completed
Study Evaluating DVS-233 SR And Venlafaxine ER In Adult Outpatients With Major Depressive Disorder

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Pfizer Clinical Trials Contact Center

1-800-718-1021

[email protected]

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Major Depressive Disorder
NCT02548949
All Genders
19+
Years
Multiple Sites

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Contact a representative by phone, email, or visiting the study website. Please see the references below:

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Pfizer Clinical Trials Contact Center

1-800-718-1021

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[email protected]

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