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Phase 2 N=248 Randomized Triple-blind Treatment

Phase 2 Study of NV-5138 in Adults With Treatment Resistant Depression

Treatment Resistant Depression

Enrolled (actual)
248
Serious AEs
1.2%
Results posted
Apr 2026
Primary outcome: Primary: Change From Baseline to Week 4 in the Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score. — -12.2; -11.6 units on a scale — p=0.7941

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
NV-5138 (Drug); matched placebo (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Navitor Pharmaceuticals, Inc.
Primary completion
Jan 2025

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline to Week 4 in the Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score.
-12.2; -11.6 0.7941
SECONDARY
Change From Baseline to Each Scheduled Week in the Montgomery-Åsberg Depression Rating Scale (MADRS) Total Score.
-7.3; -5.8; -8.6; -8.9; -10.5; -10.3 0.1727
SECONDARY
Change From Baseline to Each Scheduled Week in the Clinical Global Impression - Severity of Illness Score (CGI-S).
-0.7; -0.6; -0.9; -0.9; -1.2; -1.0 0.6304
SECONDARY
Change From Baseline to Each Scheduled Week in the The Hamilton Depression Rating Scale - 6 Items (HAM-D6) Total Score.
-2.5; -2.0; -3.0; -3.1; -3.9; -3.9 0.2689
SECONDARY
Suicidal Ideation and Behavior as Measured by the Columbia-Suicide Severity Rating Scale (C-SSRS)
16; 13; 0; 0; 11; 7

Summary

This study will evaluate the efficacy and safety of NV-5138 in adults with TRD

Eligibility Criteria

Inclusion Criteria

  • Male or female, aged 18 to 70 years at Screening.
  • Diagnosis of Major Depressive Disorder (MDD) according to the Diagnostic and Statistical Manual of Mental Disorders, 5th Edition (DSM-5) for either recurrent or single episode MDD without psychotic features that is confirmed by the Mini International Neuropsychiatric Interview (MINI).
  • Montgomery-Asberg Depression Rating Scale (MADRS) Total Score of ≥24 for the current MDE at all Screening visits and Baseline (Day 1).
  • CGI-S score of ≥4 (moderately ill or worse) at the Screening visits and Baseline.
  • History of inadequate response to ≥1 but ≤4 prior ADT therapies (including the current ADT for the current MDE) ≥ 2 weeks at Screening and ≥ 8 weeks at Baseline.
  • Stable therapeutic dose of one of the following ADTs for the current MDE for ≥2 weeks prior to Screening and maintain the therapeutic dose throughout the study: citalopram, escitalopram, paroxetine, fluoxetine, sertraline, duloxetine, venlafaxine (IR or XR), desvenlafaxine, vilazodone, levomilnacipran, vortioxetine, bupropion or dextromethorphan//bupropion.
  • Detectable blood level of the approved ADT at Visits 1 and 2 of the Screening Period.

Exclusion Criteria

  • MADRS Total Score improvement of ≥25% from the highest to the lowest score during the Screening Period and Baseline.
  • Clinically significant abnormal laboratory profiles, vital signs, or electrocardiograms (ECGs), per Investigator judgment.
  • Judged by the Investigator to be at significant risk for suicide or answers 'Yes' to items 4 or 5 on the Suicidal Ideation section of the C-SSRS in the 1 year before Screening; a history of suicide attempt in the last 2 years; or more than 2 lifetime suicide attempts.
  • History of psychotic disorder, including but not limited to schizophrenia, MDD with psychotic features, or bipolar I/II disorder with and without psychotic features.
  • Diagnosis within 12 months before Screening or current diagnosis of PTSD, OCD, panic disorder, intellectual disability, autism, acute stress disorder, or Cluster A or B personality disorder (per DSM-5 criteria).
  • History of substance use disorder within 6 months prior to Screening or currently using or had positive results (UDS) at Screening or Baseline for drugs of abuse.
  • History of alcohol and cannabis use disorder within 6 months prior to Screening and had a positive alcohol test at Baseline or a positive UDS for cannabis at Screening.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05066672). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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