Phase 2
N=248
Phase 2 Study of NV-5138 in Adults With Treatment Resistant Depression
Treatment Resistant Depression
Bottom Line
View on ClinicalTrials.gov: NCT05066672 ↗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
| Outcome | Result | p-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.
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.