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Depressive DisorderPhase 3NCT01727726

A Study of Flexible-dose Brexpiprazole as Adjunctive Therapy in the Treatment of Adults With Major Depressive Disorder, the Delphinus Trial

A Phase 3 study testing Brexpiprazole and Seroquel XR in people with Depressive Disorder and Depression, run by Otsuka Pharmaceutical Development & Commercialization, Inc. at 76 sites in 7 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

To compare the efficacy of brexpiprazole (flexible dose) with placebo as adjunctive therapy to an assigned open label antidepressant therapy (ADT) in the proposed subject population with MDD. Read more about this study

Who is it for?
Ages 18 to 65 years
What is being tested?
Brexpiprazole and Seroquel XR
Type of treatment
Pill or oral medicine
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
2,182 participants
Where
76 sitesin 7 countries
Study dates
Dec 2012to 10 Nov 2016
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Male and female outpatients 18 to 65 years of age, inclusive, at the time of informed consent.
  • Subjects with both a diagnosis of MDD, and in a current major depressive episode, as defined by DSM-IV-TR criteria
  • Subjects willing to discontinue all prohibited psychotropic medications to meet protocol-required washouts prior to and during the trial period.

Who cannot join

  • Females who are breast-feeding and/or who have a positive pregnancy test result during screening prior to receiving trial medication
  • Subject has a current Axis I (DSM-IV-TR) diagnosis of: dementia, Schizophrenia, Bipolar, Eating disorder , Obsessive-compulsive disorder, Panic disorder, Posttraumatic stress disorder
  • Subjects experiencing hallucinations, delusions or any psychotic symptomatology in the current major depressive episode.
  • Subjects who have met DSM-IV-TR criteria for substance abuse or dependence within the past 180 days
  • Subjects currently treated with insulin for diabetes.
  • Subjects with uncontrolled hypertension
Show all 11Show fewer
  • Subjects with known ischemic heart disease or history of myocardial infarction, congestive heart failure, angioplasty, stenting, or coronary artery bypass Surgery
  • Subjects with a positive drug screen for cocaine, marijuana, or other illicit drugs
  • Inability to swallow tablets or tolerate oral medication
  • Abnormal laboratory test results, vital signs and ECG results
  • Subjects who previously participated in any prior brexpiprazole clinical trial.

Trial locations and contacts

76 sites in 7 countries.

76 sites in 7 countries

United States44 sites
  • Study site

    Baltimore, Maryland

  • Study site

    Bellevue, Washington

  • Study site

    Bellflower, California

  • Study site

    Belmont, Massachusetts

  • Study site

    Beverly Hills, California

  • Study site

    Birmingham, Alabama

  • Study site

    Brown Deer, Wisconsin

  • Study site

    Columbus, Ohio

  • Study site

    Costa Mesa, California, 92626

  • Study site

    Creve Coeur, Missouri

  • Study site

    Dallas, Texas

  • Study site

    Dayton, Ohio

  • Study site

    Decatur, Georgia

  • Study site

    Edmond, Oklahoma, 73013

  • Study site

    Gainesville, Florida

  • Study site

    Glendale, California

  • Study site

    Herndon, Virginia

  • Study site

    Irvine, California

  • Study site

    Jacksonville, Florida

  • Study site

    Jacksonville Beach, Florida

  • Study site

    Kirkland, Washington

  • Study site

    Lake Charles, Louisiana

  • Study site

    Lebanon, New Hampshire

  • Study site

    Leesburg, Florida

  • Study site

    Little Rock, Arkansas

  • Study site

    Melbourne, Florida

  • Study site

    Miami, Florida, 33015

  • Study site

    Miami, Florida, 33145

  • Study site

    Murray, Utah

  • Study site

    New York, New York, 10003

  • Study site

    New York, New York, 10168

  • Study site

    Oakland Park, Florida

  • Study site

    Orange City, Florida

  • Study site

    Orlando, Florida

  • Study site

    Phoenix, Arizona

  • Study site

    Portland, Oregon

  • Study site

    Redlands, California

  • Study site

    Richmond, Virginia

  • Study site

    Roslindale, Massachusetts

  • Study site

    Salem, Oregon

  • Study site

    San Diego, California

  • Study site

    Seattle, Washington

  • Study site

    Upland, California

  • Study site

    Watertown, Massachusetts, 02472

Other trials in United States

Russia9 sites
  • Study site

    Arkhangelsk, 163530

  • Study site

    Moscow, 107076

  • Study site

    Moscow, 127083

  • Study site

    Saint Petersburg, 190020

  • Study site

    Saint Petersburg, 191040

  • Study site

    Saint Petersburg, 192019

  • Study site

    Saint Petersburg, 199034

  • Study site

    Smolensk

  • Study site

    Tonnelniy

Other trials in Russia

Poland7 sites
  • Study site

    Bełchatów

  • Study site

    Bydgoszcz

  • Study site

    Gdynia

  • Study site

    Kielce

  • Study site

    Lublin

  • Study site

    Tuszyn

  • Study site

    Wroclaw

Other trials in Poland

France6 sites
  • Study site

    Dijon

  • Study site

    Douai

  • Study site

    Élancourt

  • Study site

    Jarnac

  • Study site

    Montepellier

  • Study site

    Orvault

Other trials in France

Serbia5 sites
  • Study site

    Belgrade, 11000

  • Study site

    Belgrade

  • Study site

    Kragujevac

  • Study site

    Niš

  • Study site

    Novi Kneževac

Other trials in Serbia

Germany4 sites
  • Study site

    Achim

  • Study site

    Mittweida

  • Study site

    Stralsund

  • Study site

    Würzburg

Other trials in Germany

Canada1 site
  • Study site

    Penticton, British Columbia

Other trials in Canada

About this study

Official title: A Phase 3, Multicenter, Randomized, Double-blind, Placebo and Active Comparator Controlled Trial of Flexible-dose Brexpiprazole (OPC-34712) as Adjunctive Therapy in the Treatment of Adults With Major Depressive Disorder, the Delphinus Trial

To compare the efficacy of brexpiprazole (flexible dose) with placebo as adjunctive therapy to an assigned open label antidepressant therapy (ADT) in the proposed subject population with MDD.

Read the detailed description

This is a trial designed to assess the safety and efficacy of brexpiprazole (flexible dose) as adjunctive therapy to an assigned known anti-depressant in depressed subjects. The trial consists of a continuous 18-week double-blind treatment period with a 30-day follow-up. Subjects who complete all trial visits through the Week 18 visit may be offered entry into an optional open-label rollover trial.

Being tested
Brexpiprazole, Seroquel XR, Placebo
Keywords
OPC-34712, brexpiprazole, Major Depressive Disorder, Adjunctive Treatment
Medical subject headings
Depressive Disorder, Depression, Depressive Disorder, Major, Mood Disorders, Mental Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • BrexpiprazoleDrug

    Also called OPC-34712

    tablet/capsule

  • Seroquel XRDrug

    tablet/capsule

  • PlaceboDrug

    tablet/capsule

Study groups in NCT01727726
Study groupRoleWhat they receive
Placebo + ADTPlacebo comparatorMatching Placebo and assigned ADT
Receives: Drug: Placebo
Brexpiprazole + ADTExperimentalBrexpiprazole, flexible dose and assigned ADT
Receives: Drug: Brexpiprazole
Seroquel XR + ADTActive comparatorSeroquel XR, flexible dose and assigned ADT
Receives: Drug: Seroquel XR

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Montgomery Asberg Depression Rating Scale (MADRS)

    To determine the efficacy of brexpiprazole (flexible dose) with placebo as adjunctive therapy by assessment of MADRS total score. The MADRS depression rating scale was used to assess the subject's level of depression by utilizing the structured interview guide for the MADRS (SIGMA). The MADRS consisted of 10 items (apparent sadness, reported sadness, inner tension, reduced sleep, reduced appetite, concentration difficulties, lassitude, inability to feel, pessimistic thoughts and suicidal thoughts), each rated 0 to 6. The overall score ranged from 0 (symptoms absent) to 60 (severe depression). Lower score indicated decreased severity of depression.

    Measured: Randomization Visit (week 8 or week 10) to End of Double-Blind Treatment (week 14 or week 16).

Secondary outcomes (8)
  1. Sheehan Disability Scale (SDS)

    To evaluate mean change in SDS score from randomization (End of Phase A) to end of Phase B. The Sheehan Disability Scale is a measurement of functional disability and impairment due to psychiatric symptoms. The SDS is a visual analogue scale that uses spatio-visual, numeric, and verbal descriptive anchors simultaneously to assess disability across the three domains ( work/social life/family life/home responsibilities). The number most representative of how much each area was disrupted by symptoms is marked along the line from 0 = not at all, to 10 = extremely. Scores of 5 and above are associated with significant functional impairment. Additionally, SDS included 2 questions related to productivity losses due to the psychiatric symptoms and impairment.

    Measured: Randomization Visit (week 8 or week 10) to End of Double-Blind Treatment (week 14 or week 16).

  2. Change From End of Phase A in MADRS Total Score for Trial Week 2 and Week 4.

    Change from end of Phase A in MADRS Total Score. The MADRS was used to assess the subject's level of depression by utilizing the structured interview guide for the MADRS (SIGMA). The MADRS depression rating scale was used to assess the subject's level of depression by utilizing the structured interview guide for the MADRS (SIGMA). The MADRS consisted of 10 items (apparent sadness, reported sadness, inner tension, reduced sleep, reduced appetite, concentration difficulties, lassitude, inability to feel, pessimistic thoughts and suicidal thoughts), each rated 0 to 6. The overall score ranged from 0 (symptoms absent) to 60 (severe depression). Lower score indicated decreased severity of depression.

    Measured: Change from baseline to week 2 and week 4 in Phase B (week 10/12 and week 12/14)

  3. Clinical Global Impression Score

    Mean change from end of Phase A in Clinical Global Impression - Severity of Illness scale (CGI-S) score and Improvement scale (CGI-I) during double-blind randomized Phase B treatment. CGI-S score assessed how mentally ill the patient was at that time. CGI-S score is calculated from 0 to 7 (0 indicates not assessed 1 = normal, not at all ill; 2 = borderline mentally ill; 3 = mildly ill; 4 = moderately ill; 5 = markedly ill; 6 = severely ill; and7 indicated among the most extremely ill patient). CGI-I score is compared to his/her condition at baseline, how much has the patient changed. CGI-I score is calculated from 0 to 7 (0 indicates not assessed and 7 indicates very much worse).

    Measured: From randomization to Phase B week 6 (14/16 weeks after randomization).

  4. MADRS Response at Week 6

    MADRS Response Rate, where response was defined as 50% reduction in MADRS Total Score, during double-blind randomized Phase B treatment.

    Measured: Phase B week 6 (14/16 weeks after randomization).

  5. Number of Participants With MADRS

    MADRS Remission Rate, where remission was defined as MADRS Total Score ≤ 10 and 50% reduction in MADRS Total Score, for every trial week visit during double-blind randomized Phase B treatment.

    Measured: Phase B week 6 (14/16 weeks after randomization).

  6. CGI-I Response Rate

    CGI-I Response rate, where response was defined as a CGI-I score of 1 or 2 (very much improved or much improved), during double-blind randomized Phase B treatment.

    Measured: Phase B week 6 (14/16 weeks after randomization).

  7. Number of Participants With Adverse Events

    To evaluate the safety and tolerability of brexpiprazole (flexible dose) as adjunctive therapy to ADT in the proposed subject population with MDD as AE variables.

    Measured: From screening (Day -28 to Day-1) upto post treatment follow-up.

  8. Sheehan Disability Scale (SDS) Individual Item Scores.

    To evaluate mean change in SDS score from randomization (End of Phase A) to end of Phase B. The Sheehan Disability Scale (a self rated questionnaire) was used for measurement of functional disability and impairment due to psychiatric symptoms. The SDS is a visual analogue scale that uses spatio-visual, numeric, and verbal descriptive anchors simultaneously to assess disability across the three domains (work/school work, social life/leisure activities and family life/home responsibilities). All domains were rated on a score scale ranged from 0 (no impairment) to 10 (most severe). Score of 5 and above indicated significant functional impairment. A total score was addition of the 3 individual scores and the total score ranged from 0 (no impairment) to 30 (most severe).

    Measured: Randomization Visit (week 8 or week 10) to End of Double-Blind Treatment (week 14 or week 16).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Nov 2012 (estimated)
  2. Study startDec 2012
  3. Primary completion17 Oct 2016
  4. Study completion10 Nov 2016

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
2,182 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01727726
Sponsor's protocol ID
331-12-282
Status last verified
May 2018
First submitted
31 Oct 2012
Last updated
8 Jun 2018
Data monitoring committee
No

Publications

  • Newcomer JW, Eriksson H, Zhang P, Meehan SR, Weiss C. Changes in Metabolic Parameters and Body Weight in Patients With Major Depressive Disorder Treated With Adjunctive Brexpiprazole: Pooled Analysis of Phase 3 Clinical Studies. J Clin Psychiatry. 2019 Oct 1;80(6):18m12680. doi: 10.4088/JCP.18m12680.

    PubMed 31577867
  • Hobart M, Zhang P, Weiss C, Meehan SR, Eriksson H. Adjunctive Brexpiprazole and Functioning in Major Depressive Disorder: A Pooled Analysis of Six Randomized Studies Using the Sheehan Disability Scale. Int J Neuropsychopharmacol. 2019 Mar 1;22(3):173-179. doi: 10.1093/ijnp/pyy095.

    PubMed 30508090

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Brexpiprazole and Seroquel XR in people with Depressive Disorder and Depression, run by Otsuka Pharmaceutical Development & Commercialization, Inc. at 76 sites in 7 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 11 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Jun 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 76 sites in United States, Russia, Poland, France, Serbia and 2 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 8 Jun 2018). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Montgomery Asberg Depression Rating Scale (MADRS) (time frame: Randomization Visit (week 8 or week 10) to End of Double-Blind Treatment (week 14 or week 16).). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01727726, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Jun 2018.

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