NCT06775379Active, not recruitingPhase 3
A Randomized Study of Azetukalner Versus Placebo in Major Depressive Disorder
A Phase 3, Randomized, Double-blind, Placebo-Controlled, Multicenter Study to Evaluate Azetukalner in Moderate-to-Severe Major Depressive Disorder
Source: ClinicalTrials.gov · Last updated 13 Oct 2026
Brief summary (registry, in English)
X-NOVA2 is a Phase 3, multicenter, randomized, double-blind, placebo-controlled study to evaluate the clinical efficacy, safety, and tolerability of azetukalner as a monotherapy in adult participants diagnosed with Major Depressive Disorder (MDD)
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 450 (estimated)
- First submitted
- 9 Jan 2025
- Start date
- 20 Dec 2024
- Primary completion date
- Oct 2026
- Lead sponsor
- Xenon Pharmaceuticals Inc.
- Diseases
- Depression
- NCT number
- NCT06775379
What you commit to
- Study type: Interventional · Phase 3
- Planned participants: 450
- From 20 Dec 2024 to the primary completion date, Oct 2026
- 45 sites in 1 country
- 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
- Participant has a current diagnosis of any of the following: MDD with seasonal pattern; Depression with peripartum or perimenopausal onset; Post traumatic stress disorder; Antisocial or borderline personality disorder (or presence of clinically significant borderline personality traits); Panic disorder and/or agoraphobia; ADHD treated with a psychostimulant, diagnosed during the current MDE, or with unstable symptoms, as judged by the investigator.
- Participant has a substance (excluding tobacco) or alcohol use disorder within the 12 months prior to screening.
- Participant has had an active suicidal plan/intent within the 6 months prior to screening, presence of suicidal behavior in the last 2 years, or \>1 suicide attempt \>24 years of age.
- Participant has a history of non-suicidal self-harm behavior in the 12 months prior to screening.
- Participant has used antidepressants or other prohibited medications (including benzodiazepines), within the 2 weeks (4 weeks for fluoxetine) or within a period less than 5 times the drug's half-life, whichever is longer, prior to randomization.
Other illness
- Participant has a primary diagnosis of a mood disorder other than MDD.
- Participant has a history of any of the following: MDD with psychotic or catatonic features; MDD with mixed features; Bipolar I or II disorder; Obsessive-compulsive disorder; Schizophrenia, primary thought disorder, or other psychotic disorder.
- Participant has a history of non-response to ≥2 antidepressant drugs of adequate dose and duration in the current MDE as determined by the Antidepressant Treatment Response Questionnaire (ATRQ).
- Participants with medical conditions that may interfere with the purpose or conduct of the study
Other
- Participant is pregnant, breastfeeding, or planning to become pregnant.
Who the study is looking for
- Adults ≥18 and ≤74 years of age and experienced their first major depressive episode (MDE) prior to 50 years of age
- Body Mass Index (BMI) ≤40 kg/m2
- Meets the Diagnostic and Statistical Manual of Mental Disorders Fifth Edition Text Revised (DSM-5-TR) criteria for current major depressive disorder and is currently in an MDE, confirmed using the Mini International Neuropsychiatric Interview (MINI)
- Participant's current MDE has a duration of ≥6 weeks and ≤24 months.
Age in the registry: 18 years to 74 years · Sex: All · Does not accept healthy volunteers
Sites (45)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Lehigh Center for Clinical Research Coordinator of this site? Confirm its status | Allentown | United States | Unknown status |
| Synexus - Atlanta Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| Advanced Discovery Research Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| Northwest Clinical Trials, Inc. Coordinator of this site? Confirm its status | Boise | United States | Unknown status |
| Boston Clinical Trials Llc Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| Integrative Clinical Trials Coordinator of this site? Confirm its status | Brooklyn | United States | Unknown status |
| New Hope Clinical Research Coordinator of this site? Confirm its status | Charlotte | United States | Unknown status |
| IMA Clinical Research Coordinator of this site? Confirm its status | Chicago | United States | Unknown status |
| CNS Clinical Research Group Coordinator of this site? Confirm its status | Coral Springs | United States | Unknown status |
| Ct Clinical Research Associates Coordinator of this site? Confirm its status | Cromwell | United States | Unknown status |
| CenExel iResearch Coordinator of this site? Confirm its status | Decatur | United States | Unknown status |
| Core Clinical Research Coordinator of this site? Confirm its status | Everett | United States | Unknown status |
| NeoClinical Research Coordinator of this site? Confirm its status | Hialeah | United States | Unknown status |
| Irvine Clinical Research Coordinator of this site? Confirm its status | Irvine | United States | Unknown status |
| Clinical Neuroscience Solutions, LLC Coordinator of this site? Confirm its status | Jacksonville | United States | Unknown status |
| Accel Research Sites Lakeland Coordinator of this site? Confirm its status | Lakeland | United States | Unknown status |
| Accel Research Sites St Petersburg-Largo Coordinator of this site? Confirm its status | Largo | United States | Unknown status |
| IMA Clinical Research - Las Vegas Coordinator of this site? Confirm its status | Las Vegas | United States | Unknown status |
| Redbird Research Coordinator of this site? Confirm its status | Las Vegas | United States | Unknown status |
| Woodland International Research Group Coordinator of this site? Confirm its status | Little Rock | United States | Unknown status |
| CalNeuro Research Group, Inc Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| Psych Atlanta, Pc Coordinator of this site? Confirm its status | Marietta | United States | Unknown status |
| Clinical Neuroscience Solutions, LLC. Coordinator of this site? Confirm its status | Memphis | United States | Unknown status |
| PharmaSouth Research Coordinator of this site? Confirm its status | Miami | United States | Unknown status |
| Quantum Clinical Trials Coordinator of this site? Confirm its status | Miami Beach | United States | Unknown status |
| Neuro-Behavioral Clinical Research Coordinator of this site? Confirm its status | North Canton | United States | Unknown status |
| Harmony Clinical Research Inc Coordinator of this site? Confirm its status | North Miami Beach | United States | Unknown status |
| Excell Research, Inc. Coordinator of this site? Confirm its status | Oceanside | United States | Unknown status |
| Pahl Pharmaceutical Professionals Llc Coordinator of this site? Confirm its status | Oklahoma City | United States | Unknown status |
| ATP Clinical Research Coordinator of this site? Confirm its status | Orange | United States | Unknown status |
| NRC Research Institute Coordinator of this site? Confirm its status | Orange | United States | Unknown status |
| Clinical Neuroscience Solutions, LLC Coordinator of this site? Confirm its status | Orlando | United States | Unknown status |
| Combined Research Orlando Phase I-IV Coordinator of this site? Confirm its status | Orlando | United States | Unknown status |
| Panhandle Research and Medical Clinic Coordinator of this site? Confirm its status | Pensacola | United States | Unknown status |
| Adams Clinical Philadelphia Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| IMA Clinical Research Phoenix Coordinator of this site? Confirm its status | Phoenix | United States | Unknown status |
| Delricht Research - Plano Coordinator of this site? Confirm its status | Plano | United States | Unknown status |
| Woodland Research Northwest Coordinator of this site? Confirm its status | Rogers | United States | Unknown status |
| Cenexel Iresearch - Savannah Coordinator of this site? Confirm its status | Savannah | United States | Unknown status |
| ELIXIA Coordinator of this site? Confirm its status | Springfield | United States | Unknown status |
| Richmond Behavioral Associates Coordinator of this site? Confirm its status | Staten Island | United States | Unknown status |
| CenExel CNS-TO (Collaborative Neuroscience Research) Coordinator of this site? Confirm its status | Torrance | United States | Unknown status |
| Sunwise Clinical Research Coordinator of this site? Confirm its status | Walnut Creek | United States | Unknown status |
| Kinetic Clinical Research, LLC Coordinator of this site? Confirm its status | West Covina | United States | Unknown status |
| Grayline Research Center Coordinator of this site? Confirm its status | Wichita Falls | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.