Evidence map›Paper›PMID 29608461›Full record

Trial reportInternational clinical psychopharmacology2018

Vilazodone efficacy in subgroups of patients with major depressive disorder: a post-hoc analysis of four randomized, double-blind, placebo-controlled trials.

Susan Kornstein, Cheng-Tao Chang, Carl P Gommoll, John Edwards

4 registry-linked trialsOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in International clinical psychopharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00285376 phase3completednot on this map

A Randomized, Double-Blind, Placebo Controlled Study Assessing the Efficacy and Safety of Vilazodone and Discovering Genetic Markers Associated With Response in Patients With Major Depressive Disorder

TypeinterventionalSponsorGenaissance PharmaceuticalsRan2006 to 2007Enrolled410ConditionsDepressive Disorder, MajorArmsvilazodone
NCT00683592 phase3completednot on this map

A Randomized, Double-blind, Placebo Controlled Study Assessing the Efficacy and Safety of Vilazodone 40 mg qd and Evaluating Genetic Biomarkers Associated With Treatment Response in Patients With Major Depressive Disorder (MDD)

TypeinterventionalSponsorForest LaboratoriesRan2008 to 2009Enrolled481ConditionsMajor Depressive DisorderArmsvilazodone, placebo
NCT01473381 phase4completednot on this map

A Double-blind, Placebo- and Active-controlled, Fixed-dose Study of Vilazodone in Patients With Major Depressive Disorder

TypeinterventionalSponsorForest LaboratoriesRan2011 to 2013Enrolled1,162ConditionsMajor Depressive DisorderArmsVilazodone, Placebo to citalopram, Placebo to vilazodone, Citalopram
NCT01473394 phase4completednot on this map

A Double-blind, Placebo-controlled, Fixed-dose Study of Vilazodone in Patients With Major Depressive Disorder

TypeinterventionalSponsorForest LaboratoriesRan2011 to 2013Enrolled518ConditionsMajor Depressive DisorderArmsDose-matched placebo, Vilazodone
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 1 country.

Susan KornsteinDepartment of Psychiatry, Virginia Commonwealth University, Richmond, Virginia.
Cheng-Tao ChangDepartment of Biostatistics, Allergan, Irvine, California.
Carl P GommollDepartment of Clinical Development, Allergan, Madison, New Jersey, USA.
John EdwardsDepartment of Clinical Development, Allergan, Madison, New Jersey, USA.
Allergan (United States) · USVirginia Commonwealth University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The efficacy of antidepressants to treat major depressive disorder (MDD) varies by patient characteristics. This post-hoc analysis evaluated the effects of vilazodone across patient subgroups in adults with MDD. Data were pooled from four trials of vilazodone (NCT00285376, NCT00683592, NCT01473394, and NCT01473381). Mean change from baseline to week 8 in Montgomery-Åsberg Depression Rating Scale (MADRS) total score, MADRS response (≥50% total score improvement), and MADRS remission (total score≤10) were analyzed in the pooled intent-to-treat population (vilazodone=1254, placebo=964) and in subgroups of patients categorized by sex, age, MDD duration, recurrent episodes, baseline MADRS total score, and current episode duration. MADRS total score improvement was significantly greater with vilazodone versus placebo in the intent-to-treat population and in all patient subgroups (P<0.001). MADRS response and remission rates significantly separated from placebo (P<0.05) regardless of age, sex, MDD duration, recurrent MDD, and baseline symptom severity [except remission in patients with very severe baseline symptoms (MADRS score≥35)] and in patients with a shorter current episode duration (≤12 months). Despite the limitations associated with analyzing uncommon outcomes (e.g. MADRS remission) in small subgroups, vilazodone was an effective treatment in multiple patient populations, including those where reduced efficacy has previously been reported: males, older individuals, patients with a longer duration of MDD, and patients with recurrent depression.

Indexed as

AdolescentAdultAgedAged, 80 and overAntidepressive AgentsDouble-Blind MethodFemaleHumansMajor Depressive DisorderMaleMiddle AgedPatient Health QuestionnairePsychiatric Status Rating ScalesTreatment OutcomeVilazodone HydrochlorideYoung AdultAntidepressive AgentsVilazodone Hydrochloride

Identifiers

PMID29608461
PMCPMC5991171
OpenAlexW2795227990

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.