Venlafaxine

Generic Name
Venlafaxine
Brand Names
Effexor
Drug Type
Small Molecule
Chemical Formula
C17H27NO2
CAS Number
93413-69-5
Unique Ingredient Identifier
GRZ5RCB1QG
Background

Venlafaxine is an antidepressant and a serotonin and norepinephrine reuptake inhibitor (SNRI). Its active metabolite, desvenlafaxine, works by blocking the reuptake of serotonin and norepinephrine, which are key neurotransmitters in mood regulation. Venlafaxine is officially approved to treat major depressive disorder (MDD), generalized anxiety disorder (GAD...

Indication

Venlafaxine is indicated for the management of major depressive disorder (MDD), generalized anxiety disorder (GAD), social anxiety disorder (SAD), and panic disorder.

Associated Conditions
Generalized Anxiety Disorder, Major Depressive Disorder (MDD), Migraine, Neuropathic Pain, Panic Disorder, Social Anxiety Disorder (SAD), Vasomotor Symptoms Associated With Menopause
Associated Therapies
-

CBT as an Adjunct to SRIs in the Treatment of BDD

First Posted Date
2005-09-21
Last Posted Date
2017-03-09
Lead Sponsor
Icahn School of Medicine at Mount Sinai
Target Recruit Count
17
Registration Number
NCT00211809
Locations
🇺🇸

Mount Sinai School of Medicine, New York, New York, United States

Pharmacological Intervention in Depression After Traumatic Brain Injury

Phase 4
Completed
Conditions
First Posted Date
2005-09-20
Last Posted Date
2017-03-17
Lead Sponsor
Virginia Commonwealth University
Target Recruit Count
100
Registration Number
NCT00205491
Locations
🇺🇸

Virginia Commonwealth University, Richmond, Virginia, United States

Venlafaxine for Hot Flashes After Breast Cancer

Phase 2
Completed
Conditions
First Posted Date
2005-09-20
Last Posted Date
2008-11-14
Lead Sponsor
Indiana University School of Medicine
Target Recruit Count
75
Registration Number
NCT00198250
Locations
🇺🇸

Indiana University Cancer Center, Indianapolis, Indiana, United States

Study Comparing Venlafaxine vs. Paroxetine in Panic Disorder

Phase 3
Completed
Conditions
First Posted Date
2005-09-19
Last Posted Date
2010-04-02
Lead Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Target Recruit Count
70
Registration Number
NCT00195598

Antidepressant Medication Plus Donepezil for Treating Late-life Depression

First Posted Date
2005-09-15
Last Posted Date
2013-02-06
Lead Sponsor
University of Pittsburgh
Target Recruit Count
220
Registration Number
NCT00177671
Locations
🇺🇸

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

Treatment of Geriatric Bipolar Mood Disorders: A Pilot Study

Phase 4
Completed
Conditions
First Posted Date
2005-09-15
Last Posted Date
2005-09-15
Lead Sponsor
University of Pittsburgh
Target Recruit Count
60
Registration Number
NCT00177567
Locations
🇺🇸

University of Pittsubrgh Medical Center, Pittsburgh, Pennsylvania, United States

🇺🇸

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States

Hippocampal Volume in Young Patients With Major Depression Before and After Combined Antidepressive Therapy

First Posted Date
2005-09-08
Last Posted Date
2020-12-14
Lead Sponsor
University of Erlangen-Nürnberg Medical School
Target Recruit Count
80
Registration Number
NCT00150839
Locations
🇩🇪

Department of Psychiatry and Psychotherapy, University Erlangen-Nuremberg, Erlangen, Bavaria, Germany

Free Venlafaxine Treatment for Marijuana Addiction and Depression - 1

Phase 2
Completed
Conditions
Interventions
First Posted Date
2005-08-18
Last Posted Date
2019-04-24
Lead Sponsor
New York State Psychiatric Institute
Target Recruit Count
123
Registration Number
NCT00131456
Locations
🇺🇸

New York State Psychiatric Institute, New York, New York, United States

A Comparison of Duloxetine Hydrochloride, Marketed Comparator, and Placebo in the Treatment of Generalized Anxiety Disorder

Phase 3
Completed
Conditions
First Posted Date
2005-07-22
Last Posted Date
2007-11-06
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
480
Registration Number
NCT00122850
Locations
🇺🇸

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Monday-Friday from 9:00 AM to 5:00 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician, Seattle, Washington, United States

A Comparison of Duloxetine Hydrochloride, Marketed Comparator, and Placebo in the Treatment of Generalized Anxiety Disorder

Phase 3
Completed
Conditions
First Posted Date
2005-07-22
Last Posted Date
2007-10-18
Lead Sponsor
Eli Lilly and Company
Target Recruit Count
560
Registration Number
NCT00122837
Locations
🇬🇧

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. test, Glasgow, Scotland, United Kingdom

© Copyright 2024. All Rights Reserved by MedPath