A Study of Aticaprant 10 Milligrams (mg) as Adjunctive Therapy in Adult Participants With MDD With Moderate-to-severe Anhedonia and Inadequate Response to Current Antidepressant Therapy (VENTURA-2)
Depressive Disorder, Major, Anhedonia
About this trial
This is an interventional treatment trial for Depressive Disorder, Major
Eligibility Criteria
Inclusion Criteria:
- Be medically stable on the basis of physical examination, medical history, vital signs, and 12-lead electrocardiogram (ECG) performed at screening and baseline
- Have a Hamilton depression rating Scale 17 item (HDRS-17) total score of 20 or higher at the first and second screening interviews and must not demonstrate a clinically significant improvement (that is, an improvement of more than 20 percent [%] on their HDRS-17 total score) between the first and the second independent HDRS-17 assessments
- Meet Diagnostic and Statistical Manual of Mental Disorders-5th edition (DSM-5) diagnostic criteria for recurrent or single episode major depressive disorder (MDD), without psychotic features, based upon clinical assessment and confirmed by the structural interview for DSM-5 Axis I disorders-clinical trials version (SCID-CT). Participants 65 years of age or older must have had the first onset of depression prior to 55 years of age
- Is currently receiving and tolerating well any one of the following selective serotonin reuptake inhibitor (SSRI) or serotonin-norepinephrine reuptake inhibitor (SNRI) for depressive symptoms at screening, in any formulation and available in the participating country/territory: citalopram, duloxetine, escitalopram, fluvoxamine, fluoxetine, milnacipran, levomilnacipran, paroxetine, sertraline, venlafaxine, desvenlafaxine at a stable dose (at a therapeutic dose level per Massachusetts General Hospital Antidepressant Treatment Response Questionnaire [MGH-ATRQ] for at least 6 weeks and with some minor to moderate symptomatic improvement greater than [>] 25%). The current antidepressant cannot be the first antidepressant treatment for the first lifetime episode of depression
- Participant's current major depressive episode, and antidepressant treatment response in the current depressive episode, must all be confirmed by the Site Independent Qualification Assessment
Exclusion Criteria:
- Participant has lack of clinically meaningful improvement (less than or equal to [<=] 25% improvement) to the current SSRI/SNRI) (that is, the one presumed to be continued in the treatment phase) assessed using the MGH-ATRQ
- Has a history or evidence of clinically meaningful noncompliance with current antidepressant therapy
- Has a history of moderate-to-severe substance use disorder including alcohol use disorder according to diagnostic and statistical manual of mental disorders-5th edition (DSM-5) criteria within 6 months before screening
- Has within the last 5 years received any prior antidepressant treatment with ketamine/esketamine, electroconvulsive therapy (that is, at least 7 treatments), vagal nerve stimulation, or a deep brain stimulation device
- Has current, or a history (past 6 months), of seizures
- Has a current homicidal ideation/intent, per the investigator's clinical judgment, or has suicidal ideation with some intent to act within 3 months prior to the start of the Screening Phase, per the investigator's clinical judgment or based on the Columbia Suicide Severity Rating Scale (C-SSRS), corresponding to a response of "Yes" on Item 4 (active suicidal ideation with some intent to act, without specific plan) or Item 5 (active suicidal ideation with specific plan and intent), or a history of suicidal behavior within the past 6 months prior to the start of the Screening Phase. Participants reporting suicidal ideation with intent to act or suicidal behavior at baseline should be excluded
- Has one or more of the following diagnoses: a) A diagnostic and statistical manual of mental disorders-5th edition (DSM-5) diagnosis (which has been the primary focus of psychiatric treatment within the past 2 years) of any of the following: panic disorder, generalized anxiety disorder social anxiety disorder, specific phobia; b) A current (in the past year) DSM-5 diagnosis of: obsessive-compulsive disorder (OCD), post-traumatic stress disorder (PTSD), anorexia nervosa, bulimia nervosa; c) A current or prior (lifetime) DSM-5 diagnosis of: a psychotic disorder or major depressive disorder (MDD) with psychotic features, bipolar or related disorders, intellectual disability, autism spectrum disorder, borderline personality disorder, antisocial personality disorder, histrionic personality disorder, narcissistic personality disorders, somatoform disorders
Sites / Locations
- University of Alabama at BirminghamRecruiting
- Prospective Research Innovations, Inc.Recruiting
- CMB Clinical TrialsRecruiting
- California Neuroscience ResearchRecruiting
- Next Level Clinical Trials, LLCRecruiting
- MCB Clinical Research Centers, LLCRecruiting
- CNS Clinical Research GroupRecruiting
- Sarkis Clinical TrialsRecruiting
- Vital Care ResearchRecruiting
- Global Medical InstitutesRecruiting
- LCC Medical Research Institute, IncRecruiting
- Florida Research Center Inc.Recruiting
- Ezy Medical ResearchRecruiting
- Felicidad Medical ResearchRecruiting
- Bravo Health Care CenterRecruiting
- APG Research, LLCRecruiting
- Combined Research OrlandoRecruiting
- CDC Research Institute LLCRecruiting
- Tandem Clinical ResearchRecruiting
- CBH HealthRecruiting
- Revive Research InstituteRecruiting
- Midwest Research GroupRecruiting
- Premier Psychiatric Research Institute, LLCRecruiting
- Erie County Medical CenterRecruiting
- Manhattan Behavioral MedicineRecruiting
- New Hope Clinical ResearchRecruiting
- Monroe Biomedical ResearchRecruiting
- Wexner Medical Center at the Ohio State UniversityRecruiting
- Conrad Clinical ResearchRecruiting
- Paradigm Research Professionals, LLCRecruiting
- Lehigh Center for Clinical ResearchRecruiting
- Global Medical InstitutesRecruiting
- R and H Clinical ResearchRecruiting
- Cedar PsychiatryRecruiting
- Core Clinical ResearchRecruiting
- Fundacion para el Estudio y Tratamiento de las Enfermedades MentalesRecruiting
- MHC - Sofia, EOODRecruiting
- DCC 'Sv. Vrach and Sv. Sv. Kuzma and Damyan', OODRecruiting
- Medical Center Hera EOODRecruiting
- Medical Center Intermedica, OODRecruiting
- Diagnostic Consulting Center Mladost - M VarnaRecruiting
- Psychiatricka ambulance, MUDr. Marta Holanova
- Neuroterapie KH, s.r.o.Recruiting
- Medical Services Prague s.r.o.Recruiting
- Institut Neuropsychiatricke peceRecruiting
- CHU Clermont-Ferrand - Hopital Gabriel MontpiedRecruiting
- Cabinet Medical des Drs Prizac-Desbonnet ScottezRecruiting
- CHU de Nantes hotel-DieuRecruiting
- Hopital Sainte AnneRecruiting
- CHRU de Tours Clinique Psychiatrique UniversitaireRecruiting
- Centrum Medyczne Care Clinic KatowiceRecruiting
- Filip Rybakowski Specjalistyczna Praktyka LekarskaRecruiting
- Indywidualna Specjalistyczna Praktyka Lekarska Agnieszka Remlinger MolendaRecruiting
- Psychomed-Svatosavsky, s.r.o.Recruiting
- Nemocnica s poliklinikou Prievidza so sidlom v BojniciachRecruiting
- Psychiatricka Ambulancia Mentum S.R.O.Recruiting
- Liptovska Nemocnica S Poliklinikou Mudr. Ivana StodoluRecruiting
- Psychiatricka Ambulancia Psycholine S.R.O.Recruiting
- Cape Town Clinical Research CentreRecruiting
- Gert Bosch - Pretoria South AfricaRecruiting
- Somerset West Clinical Research UnitRecruiting
- Taipei Veterans General HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Aticaprant
Placebo
Participants will receive Aticaprant 10 milligrams (mg) tablet orally, once daily for 42 days during double-blind (DB) treatment phase in addition to their current antidepressant selective serotonin reuptake inhibitor/serotonin-norepinephrine reuptake inhibitor (SSRI/SNRI) therapy. Participants who will complete the DB treatment phase (Day 43) may be eligible to participate in a separate 52-week open-label long-term safety study 67953964MDD3003.
Participants will receive matching placebo tablet orally, once daily for 42 days during DB treatment phase in addition to their current antidepressant SSRI/SNRI therapy. Participants who will complete the DB treatment phase (Day 43) may be eligible to participate in a separate 52-week open-label long-term safety study 67953964MDD3003.