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NMRA US Equity

Neumora Therapeutics, Inc.Health Care · Biological Products, (No Diagnostic Substances) · CIK 1885522 · FY ends Dec 31
$1.64
+0.00 (+0.00%)
USD · as of 2026-08-19 · marketstack
7 registered studies · 1 active

Studies where NMRA is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

7 interventional · 1 with posted results

Held by 11 tracked-famous managers (TWO SIGMA INVESTMENTS, LP, RENAISSANCE TECHNOLOGIES LLC, MARSHALL WACE, LLP, CITADEL ADVISORS LLC, MILLENNIUM MANAGEMENT LLC, +6 more) · FINRA short interest 11.0 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
Study to Assess the Safety and Effectiveness of NMRA-335140-501NCT06029439Safety and tolerability assessments based on Treatment Emergent Adverse Events (TEAEs) and validated clinical scalesOpen-label · TreatmentPhase 3Active, not recruitingDrug: NMRA-335140Major Depressive Disorder1,000Jun 2027≤ 314 d2026-06-09
Study to Assess the Effects of Oral NMRA-335140 Versus Placebo in Participants With Major Depressive DisorderNCT06058013Change from Baseline to Week 6 in the Montgomery-Asberg Depression Rating Scale (MADRS) total scoreRandomized · Quadruple-masked · TreatmentPhase 3CompletedDrug: NMRA-335140, PlaceboMajor Depressive Disorder4302026-05-06actual2026-07-06
Study to Assess the Effects of Oral NMRA-335140 in Participants With Major Depressive DisorderNCT06058039Change from Baseline to Week 6 in the Montgomery-Asberg Depression Rating Scale (MADRS) total scoreRandomized · Quadruple-masked · TreatmentPhase 3CompletedDrug: NMRA-335140, PlaceboMajor Depressive Disorder4222026-05-04actual2026-07-06
Study to Evaluate the Effects of NMRA-323511 Among Healthy Elderly and Adults With Agitation Associated With Dementia Due to Alzheimer's DiseaseNCT06546995Part A: Safety and Tolerability Assessments Based on Treatment Emergent Adverse Events (TEAEs) and Validated Clinical ScalesRandomized · Double-masked · TreatmentPhase 1CompletedDrug: NMRA-323511, PlaceboAlzheimer's Disease, Healthy Elderly872025-11-19actual2026-05-22
To Evaluate the Effects of NMRA-335140 on Symptoms of Major Depression in Participants With Bipolar II Disorder.NCT06429722Change from Baseline to Week 6 in the Montgomery-Asberg Depression Rating Scale (MADRS) total scoreRandomized · Quadruple-masked · TreatmentPhase 2CompletedDrug: NMRA-335140 80 mg, PlaceboMajor Depressive Episode Associated With Bipolar II Disorder182025-04-09actual2026-03-30
Study to Evaluate the Effects of Oral NMRA-335140 Versus Placebo in Participants With Major Depressive DisorderNCT06029426Change from Baseline to Week 6 in the Montgomery Asberg Depression Rating Scale (MADRS) total scoreRandomized · Quadruple-masked · TreatmentPhase 3CompletedDrug: NMRA-335140, PlaceboMajor Depressive Disorder3832024-12-03actual2025-11-26
Study in Major Depressive Disorder With NMRA-335140 (BTRX-335140) vs PlaceboNCT04221230results2025-05-29Change From Baseline in Hamilton Depression Rating Scale (HAMD-17) Total Score at Weeks 8Randomized · Triple-masked · TreatmentStudy Protocol · Statistical Analysis PlanPhase 2CompletedDrug: NMRA-335140, PlaceboMajor Depressive Disorder2042022-04-08actual2025-05-29

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19