AGN-241751 in the Treatment of Major Depressive Disorder

Phase 2

Completed

Conditions: Depressive Disorder, Major

Interventions: Drug: AGN-241751
Drug: Placebo

Registration Number: NCT03586427

Lead Sponsor: Gate Neurosciences, Inc

Brief Summary: The purpose of this study is to evaluate the efficacy at 1 day post initial oral dose of AGN-241751 compared with placebo in participants with Major Depressive Disorder (MDD).

Detailed Description: Not available

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 251

Inclusion Criteria

Written informed consent from the participant has been obtained prior to any study -related procedures (as described in Appendix 3).
Male or female participants must be 18 to 65 years of age, inclusive, at the time of signing the informed consent.
Meet Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) criteria for MDD (based on confirmation from the modified Structured Clinical Interview for DSM disorders [SCID]), with a current major depressive episode of at least 8 weeks and not exceeding 18 months in duration at Visit 1.
Have a minimum score of 26 on the rater-administered Montgomery-Asberg depression rating scale (MADRS) and a minimum score of 24 on the computer-administered MADRS at both Visit 1 (Screening) and Visit 2 (Baseline).
Have a difference of no greater than 7 points between the rater-administered MADRS and computer-administered MADRS at both Visit 1 (Screening) and Visit 2 (Baseline).
Have a clinical global impression-severity (CGI-S) score ≥ 4 at both Visit 1 (Screening) and Visit 2 (Baseline).
Have a negative serum β-human chorionic gonadotropin (β-hCG) pregnancy test if a woman of childbearing potential (WOCBP).
Female participants willing to minimize the risk of becoming pregnancy for the duration of the clinical study and follow-up period. A female participant is eligible to participate if she is not pregnant, not breastfeeding, and at least one of the following conditions applies:
not a WOCBP OR
A WOCBP who agrees to follow the contraceptive guidance in Appendix 5 of protocol during the treatment period and for at least 5 terminal half-lives after the last dose of study treatment.
Male participants willing to minimize the risk of inducing pregnancy for the duration of the clinical study and follow-up period. A male participant must agree to use contraception as detailed in Appendix 5 of this protocol during the treatment period and for at least 5 terminal half-lives after the last dose of study treatment and refrain from donating sperm during this period.
Able, as assessed by the investigator, and willing to follow study instructions and likely to complete all required study visits.
Normal physical-examination findings, clinical-laboratory test results, and electrocardiogram (ECG) results from Visit 1 (Screening) or abnormal results that are determined to be not clinically significant by the investigator.
Body mass index (BMI) within the range 18 and 40 kg/m^2 (inclusive).
Eligibility confirmed through a formal adjudication process (see Section 9 Diagnostic Assessments).

Exclusion Criteria

Psychiatric and Treatment-Related Criteria

DSM-5-based diagnosis of any disorder other than MDD that was the primary focus of treatment within 6 months before Visit 1. Comorbid generalized anxiety disorder, social anxiety disorder, or specific phobias are acceptable provided they play a secondary role in the balance of symptoms and are not the primary driver of treatment decisions.
Lifetime history of meeting DSM-5 criteria for:
Schizophrenia spectrum or other psychotic disorder
Bipolar or related disorder
Major neurocognitive disorder
Neurodevelopmental disorder of greater than mild severity or of a severity that impacts the participant's ability to consent, follow study directions, or otherwise safely participate in the study
Dissociative disorder
Posttraumatic stress disorder
MDD with psychotic features
History of meeting DSM-5 criteria for alcohol or substance use disorder (other than nicotine or caffeine) within the 6 months before Visit 1.
DSM-5-based diagnosis of any personality disorder of sufficient severity to interfere with participation in this study in the opinion of the investigator.
History (based on participant report and/or medical records, and investigator judgment) of:
Inadequate response to electroconvulsive therapy (ECT), a monoamine oxidase inhibitor, ketamine, or adjunctive treatment with an antipsychotic
Treatment with clozapine or any depot antipsychotic
ECT, vagus nerve stimulation, transcranial magnetic stimulation, or any experimental central nervous system treatment during the current episode or in the 6 months before Visit 1 (whichever is longer)
Tardive dyskinesia, serotonin syndrome, or neuroleptic malignant syndrome
Having received:
Anticonvulsant/mood stabilizer, within 1 year prior to Visit 1
Antipsychotic in the current episode, with the exception of quetiapine given for insomnia ≤ 50 mg/day provided it can be safely discontinued prior to Visit 2
Combination therapy of 2 or more antidepressant therapies (ADTs) in the current episode if given for depression at adequate dose and duration
ADT augmentation agent in the current episode
Lifetime history of nonresponse to ≥ 2 antidepressants after adequate trials (adequate treatment is defined as at least 6 weeks at an adequate dose(s) based on approved package insert recommendations) or a non-response to an antidepressant after adequate treatment for the current major depressive episode.
Positive result at Visit 1 from the urine drug screen (UDS) test for any prohibited medication. Exception: participants with a positive UDS at Visit 1 for opiates, cannabinoids, or episodic use of benzodiazepines may be allowed in the study provided:
The drug was used for a legitimate medical purpose;
The drug can be discontinued prior to participation in the study (except for episodic use of benzodiazepines which may be continued); and
A repeat UDS is negative for these substances prior to enrollment (except for episodic use of benzodiazepines which may be continued)
Suicide risk, as determined by meeting any of the following criteria:
A suicide attempt within the past year
Significant risk, as judged by the investigator, based on the psychiatric interview or information collected in the C-SSRS at Visit 1 (Screening) or Visit 2 (Baseline)
MADRS Item 10 score ≥ 5 at Visit 1 (Screening) or Visit 2 (Baseline) on the MADRS
At imminent risk of injuring self or others or causing significant damage to property, as judged by the investigator.
Requiring concomitant treatment with any of the prohibited medications, supplements, or herbal products listed in Appendix 6 of protocol, including any psychotropic drug or any drug with psychotropic activity, except as described in Section 7.7.2. of protocol.
Prior participation in any investigational study of AGN-241751.
Initiation or termination of psychotherapy for depression within the 3 months preceding Visit 1, or plans to initiate, terminate, or change such therapy during the course of the study. (Support meetings or counselling [eg, marital counselling] are allowed provided they are no more frequent than weekly and do not have treatment of depression as their objective).
Ongoing treatment with phototherapy, or termination of phototherapy within 1 month of Visit 1.
Known allergy or sensitivity to the study medication or its components.

Other Medical Criteria

BMI < 18 kg/m^2 or > 40 kg/m^2 at screening.
Females who are pregnant, breastfeeding, or planning to become pregnant or breastfeed during the study.
WOCBP and male partners of WOCBP, not using a reliable means of contraception (Appendix 5 of protocol).
Participant has a condition or is in a situation which, in the investigator's opinion, may put the participant at significant risk, may confound the study results, or may interfere significantly with the participant's participation in the study.
Any cardiovascular disease that is clinically significant, unstable, or decompensated.
Heart rate (supine) of ≤ 45 beats per minute (bpm) or ≥ 120 bpm, or any heart rate that is clinically symptomatic at Visit 1 or Visit 2 based upon vital signs.
Any systolic and/or diastolic blood pressure (BP) that is symptomatic or clinically significant in the opinion of the investigator.
History of congenital QTc prolongation or QTc prolongation (screening ECG with QTcF ≥ 450 msec for men and QTcF ≥ 470 msec for women).
Hypothyroidism or hyperthyroidism, unless stabilized on appropriate pharmacotherapy with no change in dosage for at least 1 month before Visit 1.
History of seizure disorder, stroke, significant head injury, tumor of the central nervous system, or any other condition that predisposes to seizure.
Known human immunodeficiency virus (HIV) infection.
Positive hepatitis C antibody on screening, with the exception of participants for whom the reflex hepatitis C virus ribonucleic acid (HCV RNA) test is negative.
Positive test for hepatitis B surface antigen and/or hepatitis B core antibody immunoglobulin M.
Screening liver enzyme test (aspartate aminotransferase [AST] and/or alanine aminotransferase [ALT]) results > 2 times the upper limit of normal (ULN).

Other Criteria

Current enrollment in an investigational drug or device study or participation in such a study within 6 months of entry into this study.
Employee, or immediate relative of an employee, of the sponsor, any of its affiliates or partners, or the study center.
Inability to speak, read, and understand the English language sufficiently to understand the nature of the study, to provide written informed consent, or to allow the completion of all study assessments.

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
AGN-241751 Dose 1	AGN-241751	AGN-241751 Dose 1 administered as 1 tablet taken orally every day
AGN-241751 Dose 2	AGN-241751	AGN-241751 Dose 2 administered as 1 tablet taken orally every day
AGN-241751 Dose 4	AGN-241751	AGN-241751 Dose 4 administered as 1 tablet taken orally every day
AGN-241751 Dose 3	AGN-241751	AGN-241751 Dose 3 administered as 1 tablet taken orally every day
Placebo	Placebo	Placebo administered as 1 tablet taken orally every day

Primary Outcome Measures

Name	Time	Method
Change From Baseline in Montgomery-Asberg Depression Rating Scale (MADRS) Total Score	Baseline to Day 1	The MADRS is a clinician-rated scale to assess depressive symptomatology during the preceding week. Participants are rated on 10 items (feelings of sadness, lassitude, pessimism, inner tension, suicidality, reduced sleep or appetite, difficulty concentrating, and lack of interest) each on a 7-point scale from 0 (no symptoms) to 6 (symptoms of maximum severity). The total score ranges from 0 to 60 with a higher score indicating more depression. A negative change score indicates improvement.

Secondary Outcome Measures

Name	Time	Method
Change From Baseline in MADRS Total Score at Week 3	Baseline to Week 3	The MADRS is a clinician-rated scale to assess depressive symptomatology during the preceding week. Participants are rated on 10 items (feelings of sadness, lassitude, pessimism, inner tension, suicidality, reduced sleep or appetite, difficulty concentrating, and lack of interest) each on a 7-point scale from 0 (no symptoms) to 6 (symptoms of maximum severity). The total score ranges from 0 to 60 with a higher score indicating more depression. A negative change score indicates improvement.

Trial Locations

Locations (24): Wake Research - Pharmacology Research Institute
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Newport Beach, California, United States
Collaborative Neuroscience Network
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Torrance, California, United States
Synexus US - Atlanta
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Atlanta, Georgia, United States
FutureSearch Trials of Dallas, LP
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Dallas, Texas, United States
Synexus US - Queens
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Jamaica, New York, United States
Finger Lakes Clinical Research
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Rochester, New York, United States
Neurobehavioral Research, Inc
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Cedarhurst, New York, United States
Clinical Neuroscience Solutions, Inc - Memphis, TN
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Memphis, Tennessee, United States
Atlanta Center for Medical Research
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Atlanta, Georgia, United States
North County Clinical Research, Inc.
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Oceanside, California, United States
Hassman Research Institute
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Berlin, New Jersey, United States
Neuro-Behavioral Clinical Research, Inc
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North Canton, Ohio, United States
Pacific Research Partners, LLC
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Oakland, California, United States
Health Initiatives Research PLLC
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Fayetteville, Arkansas, United States
Synexus US - Cerritos
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Cerritos, California, United States
Pillar Clinical Research
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Lincolnwood, Illinois, United States
Elite Clinical Trials, Inc.
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Wildomar, California, United States
Boston Clinical Trials
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Boston, Massachusetts, United States
Eastside Comprehensive Medical Center
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New York, New York, United States
Center for Emotional Fitness
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Cherry Hill, New Jersey, United States
Research Strategies of Memphis, LLC
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Memphis, Tennessee, United States
Northwest Clinical Research Center
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Bellevue, Washington, United States
IPS Research
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Oklahoma City, Oklahoma, United States
Donald J. Garcia, Jr., MD, PA
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Austin, Texas, United States