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
Sites (63)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Dr. Ivo Natsov Outpatient Clinic For Individual Practice For Specialized Medical Care In Psychiatry ET Coordinator of this site? Confirm its status | Cherven Bryag | Bulgaria | Completed |
| Medical Center Lifemed EOOD Coordinator of this site? Confirm its status | Kirdzhali | Bulgaria | Completed |
| Medical Center Akademica EOOD Coordinator of this site? Confirm its status | Sofia | Bulgaria | Completed |
| Medical Center Intermedica Ltd. Coordinator of this site? Confirm its status | Sofiya | Bulgaria | Completed |
| Diagnostic And Consultation Centre St.Vrach And St.St. Kuzma And Damian OOD Coordinator of this site? Confirm its status | Sofiya | Bulgaria | Completed |
| Multiprofile Hospital For Active Treatment - Targovishte AD Coordinator of this site? Confirm its status | Targovishte | Bulgaria | Completed |
| Diagnostics-Consultancy Center Mladost M Varna OOD Coordinator of this site? Confirm its status | Varna | Bulgaria | Completed |
| Brain-Soultherapy s.r.o. Coordinator of this site? Confirm its status | Kladno | Czechia | Completed |
| A-Shine s.r.o. Coordinator of this site? Confirm its status | Plzen 3 | Czechia | Completed |
| INEP medical s.r.o. Coordinator of this site? Confirm its status | Prague | Czechia | Completed |
| Nervenärztliche Praxis Frau Dr. Kirsten Hahn Coordinator of this site? Confirm its status | Berlin | Germany | Completed |
| Emovis GmbH Coordinator of this site? Confirm its status | Berlin | Germany | Completed |
| Charite Universitaetsmedizin Berlin KöR Coordinator of this site? Confirm its status | Berlin | Germany | Completed |
| Klinische Forschung Berlin-Mitte GmbH Coordinator of this site? Confirm its status | Berlin | Germany | Completed |
| Klinische Forschung Hamburg GmbH Coordinator of this site? Confirm its status | Hamburg | Germany | Completed |
| Lahdelma Consulting Oy Coordinator of this site? Confirm its status | Helsinki | Finland | Completed |
| Oulu Mentalcare Oy Coordinator of this site? Confirm its status | Oulu | Finland | Completed |
| Clinical Research Services Turku -CRST Oy Coordinator of this site? Confirm its status | Turku | Finland | Completed |
| Centre Hospitalier Universitaire D'Angers Coordinator of this site? Confirm its status | Angers | France | Completed |
| University Hospital Of Clermont-Ferrand Coordinator of this site? Confirm its status | Clermont Ferrand Cedex 1 | France | Completed |
| Desbonnet Recherche Coordinator of this site? Confirm its status | Douai | France | Completed |
| Centre Hospitalier Georges Mazurelle- EPSM Mazurelle Coordinator of this site? Confirm its status | La Roche sur Yon | France | Completed |
| Centre Hospitalier Universitaire De Montpellier Coordinator of this site? Confirm its status | Montpellier Cedex 5 | France | Completed |
| Centre Hospitalier Universitaire de Nîmes Coordinator of this site? Confirm its status | Nîmes | France | Completed |
| Centre Hospitalier Henri Laborit Coordinator of this site? Confirm its status | Poitiers Cedex | France | Completed |
| Prywatne Gabinety Lekarskie „Promedicus” Anna Agnieszka Tomczak Coordinator of this site? Confirm its status | Białystok | Poland | Completed |
| PROMENTE Sp. z o.o. Coordinator of this site? Confirm its status | Bydgoszcz | Poland | Completed |
| E4r&D Sp. z o.o. Coordinator of this site? Confirm its status | Gdansk | Poland | Completed |
| Centrum Medyczne Luxmed Sp.z. o.o. Coordinator of this site? Confirm its status | Lublin | Poland | Completed |
| Indywidualna Specjalistyczna Praktyka Lekarska Agnieszka Remlinger Molenda Coordinator of this site? Confirm its status | Suchy Las | Poland | Completed |
| Ginemedica Sp. z o.o. Coordinator of this site? Confirm its status | Wroclaw | Poland | Completed |
| ProbarE i Stockholm AB Coordinator of this site? Confirm its status | Lund | Sweden | Completed |
| ProbarE i Stockholm AB Coordinator of this site? Confirm its status | Stockholm | Sweden | Completed |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Austin | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Berlin | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Brandon | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Cerritos | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Charlotte | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Decatur | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | DeSoto | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Fort Worth | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Hialeah | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Irvine | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Jacksonville | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Long Beach | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Miami Beach | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Miami Springs | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | New Haven | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Omaha | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Palm Bay | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Pembroke Pines | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Plano | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Pompano Beach | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Saint Augustine | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | San Diego | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | San Francisco | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Savannah | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Springfield | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | Staten Island | United States | Unknown status |
| Neumora Investigator Site Coordinator of this site? Confirm its status | St Louis | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.