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.
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
- Conditions the study is for
- Depressive Disorder, Depression, Depressive Disorder, Major
- 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
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
Poland7 sites
Study site
Bełchatów
Study site
Bydgoszcz
Study site
Gdynia
Study site
Kielce
Study site
Lublin
Study site
Tuszyn
Study site
Wroclaw
France6 sites
Study site
Dijon
Study site
Douai
Study site
Élancourt
Study site
Jarnac
Study site
Montepellier
Study site
Orvault
Serbia5 sites
Study site
Belgrade, 11000
Study site
Belgrade
Study site
Kragujevac
Study site
Niš
Study site
Novi Kneževac
Germany4 sites
Study site
Achim
Study site
Mittweida
Study site
Stralsund
Study site
Würzburg
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.
- Conditions
- Depressive Disorder, Depression, Depressive Disorder, Major, Mood Disorders, Mental Disorders
- 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 group | Role | What they receive |
|---|---|---|
| Placebo + ADT | Placebo comparator | Matching Placebo and assigned ADT Receives: Drug: Placebo |
| Brexpiprazole + ADT | Experimental | Brexpiprazole, flexible dose and assigned ADT Receives: Drug: Brexpiprazole |
| Seroquel XR + ADT | Active comparator | Seroquel 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.
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)
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).
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)
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).
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).
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).
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).
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.
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.
- First posted16 Nov 2012 (estimated)
- Study startDec 2012
- Primary completion17 Oct 2016
- Study completion10 Nov 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Depressive DisorderStudies of the same condition, open and under way.
- More trials run by Otsuka Pharmaceutical Development & Commercialization, Inc.The sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Mary Hobart, Study director, Otsuka Pharmaceutical Development & Commercialization, Inc.
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
- Results posted
- Yes, on ClinicalTrials.gov
- 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 31577867Hobart 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
Study at a glance
From the registry record, last updated by the sponsor on 8 Jun 2018. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT01727726
- Acronym / sponsor ID
- 331-12-282
- Conditions
- Depressive Disorder, Depression, Depressive Disorder, Major, Mood Disorders, Mental Disorders
- Keywords
- OPC-34712, brexpiprazole, Major Depressive Disorder, Adjunctive Treatment
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 2,182 participants (actual)
- Lead sponsor
- Otsuka Pharmaceutical Development & Commercialization, Inc.Industry (pharma, biotech, devices)
- Study start
- Dec 2012
- Primary completion
- 17 Oct 2016 (actual)
- Study completion
- 10 Nov 2016 (actual)
- First posted
- 16 Nov 2012 (estimated)
- Results
- Posted 8 Jun 2018
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Placebo + ADT | Placebo comparator | Drug: PlaceboMatching Placebo and assigned ADT |
| Brexpiprazole + ADT | Experimental | Drug: BrexpiprazoleBrexpiprazole, flexible dose and assigned ADT |
| Seroquel XR + ADT | Active comparator | Drug: Seroquel XRSeroquel XR, flexible dose and assigned ADT |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- 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.
Key exclusion criteria (11 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| BrexpiprazoleAlso: OPC-34712tablet/capsule | Drug | Brexpiprazole + ADT |
| Seroquel XRtablet/capsule | Drug | Seroquel XR + ADT |
| Placebotablet/capsule | Drug | Placebo + ADT |
Primary outcome
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).
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.
8 secondary outcomes
Sheehan Disability Scale (SDS)
Time frame: Randomization Visit (week 8 or week 10) to End of Double-Blind Treatment (week 14 or week 16).
Change From End of Phase A in MADRS Total Score for Trial Week 2 and Week 4.
Time frame: Change from baseline to week 2 and week 4 in Phase B (week 10/12 and week 12/14)
Clinical Global Impression Score
Time frame: From randomization to Phase B week 6 (14/16 weeks after randomization).
MADRS Response at Week 6
Time frame: Phase B week 6 (14/16 weeks after randomization).
Number of Participants With MADRS
Time frame: Phase B week 6 (14/16 weeks after randomization).
CGI-I Response Rate
Time frame: Phase B week 6 (14/16 weeks after randomization).
Number of Participants With Adverse Events
Time frame: From screening (Day -28 to Day-1) upto post treatment follow-up.
Sheehan Disability Scale (SDS) Individual Item Scores.
Time frame: Randomization Visit (week 8 or week 10) to End of Double-Blind Treatment (week 14 or week 16).
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Jun 2018.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 31577867Newcomer 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.
- Derived from this study: PubMed 30508090Hobart 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Mary Hobart study director
Otsuka Pharmaceutical Development & Commercialization, Inc.
76 sites in 7 countries: see every site and its status.
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.