Evidence map›Paper›PMID 41055581›Full record

Trial reportThe international journal of neuropsychopharmacology2025

Adjunctive brexpiprazole in patients with major depressive disorder who show minimal or partial response to antidepressant treatment: post hoc analysis of randomized controlled trials.

Shivani Kapadia, Zhen Zhang, Ferhat Ardic, Mehul Patel, Michael E Thase, George I Papakostas

3 registry-linked trialsAbstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in The international journal of neuropsychopharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 3 registered trials, which are not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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.

NCT01360632 phase3completednot on this map

A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Trial of the Safety and Efficacy of Two Fixed Doses of OPDC-34712 as Adjunctive Therapy in the Treatment of Adults With Major Depressive Disorder, the Polaris Trial

TypeinterventionalSponsorOtsuka Pharmaceutical Development & Commercialization, Inc.Ran2011 to 2013Enrolled1,539ConditionsDepressive Disorder, Depression, Depressive Disorder, Major, Mood DisordersArmsOPC-34712 + ADT, Placebo + ADT
NCT01360645 phase3completednot on this map

A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Trial of the Safety and Efficacy of Fixed Dose OPC-34712 as Adjunctive Therapy in the Treatment of Adults With Major Depressive Disorder, the Pyxis Trial

TypeinterventionalSponsorOtsuka Pharmaceutical Development & Commercialization, Inc.Ran2011 to 2013Enrolled826ConditionsDepressive Disorder, Depression, Depressive Disorder, Major, Mood DisordersArmsOPC-34712 + ADT, Placebo + ADT
NCT02196506 phase3completednot on this map

A Phase 3, Multicenter, Randomized, Double-blind, Placebo-controlled Trial of the Safety and Efficacy of Fixed-dose Brexpiprazole (OPC-34712) as Adjunctive Therapy in the Treatment of Adults With Major Depressive Disorder With and Without Anxious Distress

TypeinterventionalSponsorOtsuka Pharmaceutical Development & Commercialization, Inc.Ran2014 to 2016Enrolled837ConditionsDepressive Disorder, Depression, Depressive Disorder, Major, Mood DisordersArmsPlacebo + ADT, Brexpiprazole +ADT
3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. 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

6 authors.

Shivani KapadiaMedical Affairs, Otsuka Pharmaceutical Development & Commercialization Inc., Princeton, NJ, United States.ORCID 0000-0002-1683-4742
Zhen ZhangMedical and Real-World Data Analytics, Otsuka Pharmaceutical Development & Commercialization Inc., Princeton, NJ, United States.
Ferhat ArdicMedical Affairs, H. Lundbeck A/S, Valby, Denmark.
Mehul PatelMedical Affairs, Otsuka Pharmaceutical Development & Commercialization Inc., Princeton, NJ, United States.
Michael E ThasePerelman School of Medicine, University of Pennsylvania and the Philadelphia Veterans Affairs Medical Center, Philadelphia, PA, United States.
George I PapakostasDepartment of Psychiatry, Clinical Trials Network and Institute, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United States.

Funding

Lundbeck LLC (Deerfield, IL)Otsuka Pharmaceutical Development & Commercialization Inc. (Princeton, NJ, USA)
6 · The paper itself

Abstract

introductionMany patients with major depressive disorder (MDD) have <50% symptom reduction on antidepressant treatment, and may benefit from an adjunctive atypical antipsychotic. This post hoc analysis aimed to investigate the efficacy and safety of adjunctive brexpiprazole in patients with minimal (>0% to <25%) and partial (≥25% to <50%) response to antidepressant treatment.

methodsData were pooled from three international, randomized, double-blind, placebo-controlled, Phase 3 trials. Adult outpatients with MDD and inadequate response to antidepressant treatments were enrolled. Patients were stratified post hoc into minimal and partial response subgroups based on their response over an 8-week prospective antidepressant treatment period. Adjunctive brexpiprazole 2-3 mg/day (versus adjunctive placebo) was investigated in a 6-week randomized treatment period. Efficacy was assessed using the Montgomery-Åsberg Depression Rating Scale (MADRS) and the Clinical Global Impressions - Severity of illness (CGI-S). Safety was assessed by treatment-emergent adverse events (TEAEs).

resultsIn patients with minimal response to antidepressant treatment (n = 663), least squares (LS) mean (SE) MADRS total score change over the randomized treatment period was -8.8 (0.3) points for antidepressant + brexpiprazole and -6.3 (0.3) points for antidepressant + placebo; the LS mean difference at Week 6 was -2.47 (95% CI, -3.38 to -1.55); P<.001; Cohen's d, 0.41. In patients with partial response to antidepressant treatment (n = 235), corresponding changes were -6.4 (0.5) and -4.9 (0.5) points; LS mean difference, -1.53 (-2.94 to -0.11); P = .035; Cohen's d, 0.28. CGI-S results aligned with MADRS results. In patients with minimal response to antidepressant treatment, the incidence of TEAEs was 196/328 (59.8%) for antidepressant + brexpiprazole and 160/335 (47.8%) for antidepressant + placebo. In patients with partial response to antidepressant treatment, corresponding values were 63/115 (54.8%) and 49/120 (40.8%).

conclusionsAdjunctive brexpiprazole may be efficacious in MDD regardless of whether patients show minimal or partial response to antidepressant treatment.

trial registrationPost hoc analysis of NCT01360645, NCT01360632, NCT02196506 (ClinicalTrials.gov). Significance Statement Depression is a common mental disorder associated with a constant feeling of sadness or lack of interest in daily life. Treatment with antidepressant medication can help to improve symptoms of depression. However, the amount of improvement varies from person to person. For people who still have symptoms on antidepressants, one option is to add brexpiprazole. Brexpiprazole is a medication that can help to improve symptoms of depression when taken with an antidepressant. Our study used data from clinical trials to look at the effects of brexpiprazole in people with either "minimal" or "partial" improvement on antidepressant. We found that, in both groups, people who added brexpiprazole had a greater improvement in symptoms than people who added a placebo (dummy drug). This means that adding brexpiprazole may help people with depression regardless of the amount of improvement they had on antidepressant alone.

Indexed as

Antidepressive AgentsMajor Depressive DisorderQuinolonesThiophenesAdultAgedDouble-Blind MethodDrug Therapy, CombinationFemaleHumansMaleMiddle AgedPsychiatric Status Rating ScalesRandomized Controlled Trials as TopicTreatment OutcomeAntidepressive AgentsbrexpiprazoleQuinolonesThiophenesclinical trialsdepressionsubgroup analysistreatment augmentationtreatment optimization

Identifiers

PMID41055581
PMCPMC12554155

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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.