MedPath

Desvenlafaxine

Generic Name
Desvenlafaxine
Brand Names
Pristiq
Drug Type
Small Molecule
Chemical Formula
C16H25NO2
CAS Number
93413-62-8
Unique Ingredient Identifier
NG99554ANW
Background

Desvenlafaxine (O-desmethylvenlafaxine) is the 0-demetyhlated active metabolite of venlafaxine. Like its parent drug, desvenlafaxine is also an antidepressant belonging to the class of serotonin-norepinephrine reuptake inhibitor (SNRI) class. It was approved by the FDA in 2008 for the treatment of adults with major depressive disorder (MDD).

MDD is a highly prevalent psychiatric disorder, with a lifetime prevalence estimate of 16% in the US alone and 12.8% in Europe. Although the exact mechanism of pathophysiology is still unknown, imbalances or deficiencies of monoamines have been heavily implicated, thus the rationale behind the use of SNRI to treat MDD. Desvenlafaxine has a very similar pharmacological, efficacy, and safety profile as venlafaxine. The major difference is the potential for drug interaction since venlafaxine is mainly metabolized by CYP2D6 while desvenlafaxine is conjugated by UGT; therefore, desvenlafaxine is less likely to cause drug-drug interaction when taken with medications affecting the CYP2D6 pathway.

Indication

Desvenlafaxine is indicated for the treatment of major depressive disorder in adults. It has also been used off-label to treat hot flashes in menopausal women.

Associated Conditions
Hot Flashes, Major Depressive Disorder (MDD)

Effectiveness of the Dual Serotonin Norepinephrine Reuptake Inhibitor Desvenlafaxine Succinate in Healthy Volunteers

Phase 1
Conditions
Healthy
Interventions
First Posted Date
2010-04-09
Last Posted Date
2011-08-08
Lead Sponsor
University of Ottawa
Target Recruit Count
20
Registration Number
NCT01101152
Locations
🇨🇦

University of Ottawa Institute of Mental Health Research, Ottawa, Ontario, Canada

Study Comparing Discontinuation Symptoms Of DVS SR In Subjects With Major Depressive Disorder (MDD)

First Posted Date
2010-01-26
Last Posted Date
2012-02-28
Lead Sponsor
Pfizer
Target Recruit Count
480
Registration Number
NCT01056289

Study Evaluating the Long-Term Safety of Desvenlafaxine Succinate Sustained-Release (DVS SR) in Subjects With Pain Associated With Diabetic Peripheral Neuropathy

Phase 3
Terminated
Conditions
Diabetic Neuropathy, Painful
Interventions
First Posted Date
2010-01-15
Last Posted Date
2023-12-11
Lead Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Target Recruit Count
237
Registration Number
NCT01050218

Study Evaluating the Effect of Desvenlafaxine on the Pharmacokinetics of Midazolam

Phase 4
Completed
Conditions
Major Depressive Disorder
Interventions
First Posted Date
2009-08-06
Last Posted Date
2011-08-15
Lead Sponsor
Pfizer
Target Recruit Count
28
Registration Number
NCT00952653
Locations
🇺🇸

Pfizer Investigational Site, New Haven, Connecticut, United States

Desvenlafaxine Succinate (DVS) for Major Depressive Disorder (MDD) in Midlife Men and Women

Phase 3
Conditions
Major Depressive Disorder
Menopausal Staging and Vasomotor Symptoms (for Females)
Interventions
First Posted Date
2009-04-28
Last Posted Date
2012-02-08
Lead Sponsor
Hamilton Health Sciences Corporation
Target Recruit Count
90
Registration Number
NCT00888862
Locations
🇨🇦

Women's Health Concerns Clinic, Hamilton, Ontario, Canada

Relapse Prevention Study Of Desvenlafaxine Succinate Sustained Release In Outpatients With Major Depressive Disorder

Phase 3
Completed
Conditions
Major Depressive Disorder
Interventions
First Posted Date
2009-04-23
Last Posted Date
2014-11-21
Lead Sponsor
Pfizer
Target Recruit Count
874
Registration Number
NCT00887224
Locations
🇿🇦

Pfizer Investigational Site, Paarl, South Africa

Study Evaluating Desvenlafaxine Succinate Sustained Release In Adults With Major Depressive Disorder

Phase 3
Completed
Conditions
Major Depressive Disorder
Interventions
First Posted Date
2009-03-18
Last Posted Date
2011-05-06
Lead Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Target Recruit Count
682
Registration Number
NCT00863798
Locations
🇺🇸

Pfizer Investigational Site, Waukesha, Wisconsin, United States

Study Evaluating Long-Term Safety of Desvenlafaxine Succinate Sustained Release With Japanese Adult Subjects in Major Depressive Disorder (MDD)

Phase 3
Completed
Conditions
Major Depressive Disorder
Interventions
First Posted Date
2009-01-29
Last Posted Date
2018-12-07
Lead Sponsor
Pfizer
Target Recruit Count
304
Registration Number
NCT00831415
Locations
🇯🇵

Pfizer Investigational Site, Tokyo, Japan

Study Evaluating Desvenlafaxine Succinate Sustained Release In Outpatients With Major Depressive Disorder

Phase 3
Completed
Conditions
Depressive Disorder, Major
Interventions
First Posted Date
2009-01-16
Last Posted Date
2011-03-10
Lead Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Target Recruit Count
437
Registration Number
NCT00824291

Study Evaluating the Safety, Tolerability and Pharmacokinetics of Desvenlafaxine Succinate SR in Healthy Chinese Male and Females

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2009-01-07
Last Posted Date
2013-01-29
Lead Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Target Recruit Count
36
Registration Number
NCT00818155
© Copyright 2025. All Rights Reserved by MedPath