Expired Study
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Montgomery, Alabama 36106


Purpose:

The purpose of the study is to evaluate the efficacy and safety of Desvenlafaxine Succinate (DVS) SR, in comparison to placebo for the treatment of Vasomotor Symptoms (VMS) in menopausal women.


Criteria:

Inclusion Criteria: - Generally healthy, postmenopausal women who seek treatment for hot flushes - Body Mass Index (BMI) less than or equal to 40 kg/m2 Exclusion Criteria: - Hypersensitivity to Venlafaxine - Myocardial infarction an/or unstable angina within 6 months of screening - History of seizure disorder


NCT ID:

NCT00683800


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Montgomery, Alabama 36106
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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