Study to Assess the Effects of Oral NMRA-335140 in Participants With Major Depressive Disorder

Launched by NEUMORA THERAPEUTICS, INC. · Sep 21, 2023

Keywords

ClinConnect Summary

This clinical trial is studying a new medication called NMRA-335140 to see how well it helps people with Major Depressive Disorder (MDD) feel better. The trial is in its third phase, meaning it is testing the medication in a larger group of people to gather more information about its effectiveness and safety. To participate, individuals must be diagnosed with MDD and have had symptoms for at least four weeks. They should also have a specific score on a depression scale to qualify.

Participants in this trial will go through a screening process to confirm their eligibility and then enter a 6-week treatment period. During this time, they will receive either NMRA-335140 or a placebo (a pill with no active medication) without knowing which one they are getting. At the end of the study, those who complete the trial and meet certain criteria may have the option to continue receiving the medication in a follow-up study. This is an important opportunity for those struggling with depression to potentially access new treatment options while contributing to medical research.

Gender

ALL

Eligibility criteria

• Key Inclusion Criteria:
• • Have a primary Diagnostic and Statistical Manual of Mental Disorders Fifth Edition Text Revised (DSM-5-TR) diagnosis of MDD without psychotic features confirmed by Structured Clinical Interview for DSM 5 Disorders, Clinical Trials Version (SCID 5 CT) at screening (this may be a first or recurrent episode).
• • Participant's current major depressive episode must be confirmed by independent assessment.
• • The symptoms of the current MDD episode have been present for more than 4 weeks prior to the Screening Visit, but no longer than 12 months prior to the Screening Visit.
• • Have a MADRS total score of 25 or higher at Screening and Baseline.
• • A change in MADRS total score between Screening and Baseline of ≤20%.
• Key Exclusion Criteria:
• • Have failed 2 or more courses of antidepressant treatment at sufficient doses for at least 6 to 8 weeks for the current MDD episode.
• • Currently or in the past year have been diagnosed with a personality disorder per the DSM-5-TR or in the past 3 years have been diagnosed with any of the following DSM-5-TR disorders: anorexia nervosa, bulimia nervosa, or binge eating disorder. Participants with comorbid generalized anxiety disorder, social anxiety disorder, simple phobias, or panic disorder for whom MDD is considered the primary diagnosis are not excluded.
• • Have a lifetime diagnosis of bipolar 1 or 2, schizophrenia, schizoaffective, schizophreniform, obsessive compulsive disorder, or post-traumatic stress disorder (PTSD).
• • Have moderate to severe substance or alcohol use disorder, per DSM-5-TR criteria, within the 12 months prior to screening (excluding nicotine).
• • Are actively suicidal (eg, any suicide attempts within the past 12 months) or are at serious suicidal risk as indicated by any current suicidal intent, including a plan, as assessed by the Columbia Suicide Severity Rating Scale (C-SSRS) (score of "YES" on suicidal ideations Item 4 or 5 within 3 months prior to Visit 1 \[Screening\]) and/or based on clinical evaluation by the Investigator; or are homicidal, in the opinion of the Investigator. Participants who are currently hospitalized for MDD symptoms or suicidality are not allowed into the study. If there is a recent history (within 3 months of screening) of hospitalization due to MDD symptoms, the participant should be discussed with the Medical Monitor for eligibility.