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NCT06058039CompletedPhase 3

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

A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Effects of Oral NMRA-335140 Versus Placebo in Participants With Major Depressive Disorder

Source: ClinicalTrials.gov · Last updated 6 Jul 2026

Brief summary (registry, in English)

This randomized, double-blind, placebo-controlled, multicenter study will evaluate the effects of NMRA-335140 (formerly BTRX-335140) on symptoms of depression in participants with Major Depressive Disorder (MDD). The study design consists of a Screening Period (up to 35 days), and a 6-week Treatment Period (during which participants will receive either NMRA-335140 or placebo). At the completion of the 6-week Treatment Period, participants who complete the study, provide informed consent, and meet the eligibility criteria may enter an open-label extension study (NMRA-335140-501).

Status (registry)
Completed
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
422 (actual)
First submitted
21 Sept 2023
Start date
21 Dec 2023
Primary completion date
4 May 2026
Lead sponsor
Neumora Therapeutics, Inc.
Diseases
Depression
NCT number
NCT06058039
EU CT number
2023-506335-15-00

What you commit to

  • Study type: Interventional · Phase 3
  • Participants enrolled: 422
  • From 21 Dec 2023 to the primary completion date, 4 May 2026
  • 63 sites in 8 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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.

Other illness

  • 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).

Other

  • Have failed 2 or more courses of antidepressant treatment at sufficient doses for at least 6 to 8 weeks for the current MDD episode.

Who the study is looking for

  • 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%.

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (63)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Dr. Ivo Natsov Outpatient Clinic For Individual Practice For Specialized Medical Care In Psychiatry ET
Coordinator of this site? Confirm its status
Cherven BryagBulgariaCompleted
Medical Center Lifemed EOOD
Coordinator of this site? Confirm its status
KirdzhaliBulgariaCompleted
Medical Center Akademica EOOD
Coordinator of this site? Confirm its status
SofiaBulgariaCompleted
Medical Center Intermedica Ltd.
Coordinator of this site? Confirm its status
SofiyaBulgariaCompleted
Diagnostic And Consultation Centre St.Vrach And St.St. Kuzma And Damian OOD
Coordinator of this site? Confirm its status
SofiyaBulgariaCompleted
Multiprofile Hospital For Active Treatment - Targovishte AD
Coordinator of this site? Confirm its status
TargovishteBulgariaCompleted
Diagnostics-Consultancy Center Mladost M Varna OOD
Coordinator of this site? Confirm its status
VarnaBulgariaCompleted
Brain-Soultherapy s.r.o.
Coordinator of this site? Confirm its status
KladnoCzechiaCompleted
A-Shine s.r.o.
Coordinator of this site? Confirm its status
Plzen 3CzechiaCompleted
INEP medical s.r.o.
Coordinator of this site? Confirm its status
PragueCzechiaCompleted
Nervenärztliche Praxis Frau Dr. Kirsten Hahn
Coordinator of this site? Confirm its status
BerlinGermanyCompleted
Emovis GmbH
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BerlinGermanyCompleted
Charite Universitaetsmedizin Berlin KöR
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BerlinGermanyCompleted
Klinische Forschung Berlin-Mitte GmbH
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BerlinGermanyCompleted
Klinische Forschung Hamburg GmbH
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HamburgGermanyCompleted
Lahdelma Consulting Oy
Coordinator of this site? Confirm its status
HelsinkiFinlandCompleted
Oulu Mentalcare Oy
Coordinator of this site? Confirm its status
OuluFinlandCompleted
Clinical Research Services Turku -CRST Oy
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TurkuFinlandCompleted
Centre Hospitalier Universitaire D'Angers
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AngersFranceCompleted
University Hospital Of Clermont-Ferrand
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Clermont Ferrand Cedex 1FranceCompleted
Desbonnet Recherche
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DouaiFranceCompleted
Centre Hospitalier Georges Mazurelle- EPSM Mazurelle
Coordinator of this site? Confirm its status
La Roche sur YonFranceCompleted
Centre Hospitalier Universitaire De Montpellier
Coordinator of this site? Confirm its status
Montpellier Cedex 5FranceCompleted
Centre Hospitalier Universitaire de Nîmes
Coordinator of this site? Confirm its status
NîmesFranceCompleted
Centre Hospitalier Henri Laborit
Coordinator of this site? Confirm its status
Poitiers CedexFranceCompleted
Prywatne Gabinety Lekarskie „Promedicus” Anna Agnieszka Tomczak
Coordinator of this site? Confirm its status
BiałystokPolandCompleted
PROMENTE Sp. z o.o.
Coordinator of this site? Confirm its status
BydgoszczPolandCompleted
E4r&D Sp. z o.o.
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GdanskPolandCompleted
Centrum Medyczne Luxmed Sp.z. o.o.
Coordinator of this site? Confirm its status
LublinPolandCompleted
Indywidualna Specjalistyczna Praktyka Lekarska Agnieszka Remlinger Molenda
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Suchy LasPolandCompleted
Ginemedica Sp. z o.o.
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WroclawPolandCompleted
ProbarE i Stockholm AB
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LundSwedenCompleted
ProbarE i Stockholm AB
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StockholmSwedenCompleted
Neumora Investigator Site
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AtlantaUnited StatesUnknown status
Neumora Investigator Site
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AustinUnited StatesUnknown status
Neumora Investigator Site
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BerlinUnited StatesUnknown status
Neumora Investigator Site
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BrandonUnited StatesUnknown status
Neumora Investigator Site
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CerritosUnited StatesUnknown status
Neumora Investigator Site
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CharlotteUnited StatesUnknown status
Neumora Investigator Site
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DecaturUnited StatesUnknown status
Neumora Investigator Site
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DeSotoUnited StatesUnknown status
Neumora Investigator Site
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Fort WorthUnited StatesUnknown status
Neumora Investigator Site
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HialeahUnited StatesUnknown status
Neumora Investigator Site
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IrvineUnited StatesUnknown status
Neumora Investigator Site
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JacksonvilleUnited StatesUnknown status
Neumora Investigator Site
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Long BeachUnited StatesUnknown status
Neumora Investigator Site
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MiamiUnited StatesUnknown status
Neumora Investigator Site
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Miami BeachUnited StatesUnknown status
Neumora Investigator Site
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Miami SpringsUnited StatesUnknown status
Neumora Investigator Site
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New HavenUnited StatesUnknown status
Neumora Investigator Site
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New YorkUnited StatesUnknown status
Neumora Investigator Site
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OmahaUnited StatesUnknown status
Neumora Investigator Site
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Palm BayUnited StatesUnknown status
Neumora Investigator Site
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Pembroke PinesUnited StatesUnknown status
Neumora Investigator Site
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PlanoUnited StatesUnknown status
Neumora Investigator Site
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Pompano BeachUnited StatesUnknown status
Neumora Investigator Site
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Saint AugustineUnited StatesUnknown status
Neumora Investigator Site
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San DiegoUnited StatesUnknown status
Neumora Investigator Site
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San FranciscoUnited StatesUnknown status
Neumora Investigator Site
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SavannahUnited StatesUnknown status
Neumora Investigator Site
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SpringfieldUnited StatesUnknown status
Neumora Investigator Site
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Staten IslandUnited StatesUnknown status
Neumora Investigator Site
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St LouisUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.