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NCT07076407Active, not recruitingPhase 3

A Randomized Study of Azetukalner Versus Placebo in Major Depressive Disorder (X-NOVA3)

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 15 Oct 2026

Brief summary (registry, in English)

X-NOVA3 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
14 Jul 2025
Start date
8 Jul 2025
Primary completion date
31 May 2027
Lead sponsor
Xenon Pharmaceuticals Inc.
Diseases
Depression
NCT number
NCT07076407

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 450
  • From 8 Jul 2025 to the primary completion date, 31 May 2027
  • 50 sites in 7 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

  • 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

Full criteria on ClinicalTrials.gov

Sites (50)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Charite - Universitatsmedizin Berline
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BerlinGermanyUnknown status
Boehm-Peters PartGmbB - Praxis fur Psychiatrie, Psychotherapie, Neurologie
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RosenheimGermanyUnknown status
Hospital Universitari Vall d'Hebron
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BarcelonaSpainUnknown status
Hospital Universitario Son Espases
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Palma de MallorcaSpainUnknown status
Suomen Terveystalo Oy
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HelsinkiFinlandUnknown status
Oulu Mentalcare Oy
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OuluFinlandUnknown status
In- Vivo Sp. z o. o.
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BydgoszczPolandUnknown status
Clinical Medical Research Sp. z o.o.
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KatowicePolandUnknown status
Specjalistyczna Praktyka Lekarska, Filip Rybakowski
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PoznanPolandUnknown status
Praktyka Lekarska Malgorzata Wojtanowska-Bogacka
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PoznanPolandUnknown status
Centru De Evaluare Si Tratament A Toxicodependentenlor Pentru Tineri Sf. Stelian
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BucharestRomaniaUnknown status
Clinica Nutrimed Cercetare Sr
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BucharestRomaniaUnknown status
Institutul Privat De Cercetari Melchisedec (ICPM) Pentru Boli Autoimune Ereditare si Rare - ICPM
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CraiovaRomaniaUnknown status
Dana Ignjatovićová, spol. s r.o
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Banská BystricaSlovakiaUnknown status
Liptovska Nemocnica S Poliklinikou Mudr. Ivana Stodolu Liptovsky Mikulas
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Liptovský MikulášSlovakiaUnknown status
Emory University - Brain Health Center
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AtlantaUnited StatesUnknown status
DelRicht Research
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AtlantaUnited StatesUnknown status
Austin Clinical Trial Partners
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AustinUnited StatesUnknown status
Pharmasite Research, Inc.
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BaltimoreUnited StatesUnknown status
Clinical Innovations, Inc.
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BellflowerUnited StatesUnknown status
Pillar Clinical Research
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BentonvilleUnited StatesUnknown status
Adams Clinical Boston
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BostonUnited StatesUnknown status
SanRo Clinical Research Group
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BryantUnited StatesUnknown status
Magnolia Clinical Research LLC
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CaryUnited StatesUnknown status
Lumina Clinical Research Center
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Cherry HillUnited StatesUnknown status
Harmonex Neuroscience Research
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DothanUnited StatesUnknown status
Gulfcoast Clinical Research Center
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Fort MyersUnited StatesUnknown status
Sarkis Clinical Trials
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GainesvilleUnited StatesUnknown status
Institute of Living
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HartfordUnited StatesUnknown status
University of Alabama at Birmingham, Huntsville Regional Medical Campus
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HuntsvilleUnited StatesUnknown status
Insight Clinical Trials
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IndependenceUnited StatesUnknown status
Smart Trials, LLC
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JeffersonUnited StatesUnknown status
Center for Neurohealth
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La JollaUnited StatesUnknown status
Activmed Practices & Research, Llc - Methuen
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MethuenUnited StatesUnknown status
Bioscience Research LLC
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Mount KiscoUnited StatesUnknown status
Fieve Clinical Research, Inc
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New YorkUnited StatesUnknown status
IMA Clinical Research
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New YorkUnited StatesUnknown status
Psychiatric Care and Research Center
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O'FallonUnited StatesUnknown status
Sooner Clinical Research
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Oklahoma CityUnited StatesUnknown status
Advanced Quality Medical Research
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Orland ParkUnited StatesUnknown status
Princeton Medical Institute
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PrincetonUnited StatesUnknown status
Boeson Research
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ProvoUnited StatesUnknown status
Equipath Health and Research Tampa Bay, Llc
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RiverviewUnited StatesUnknown status
St. Charles Psychiatric Associates - Midwest Research Group
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Saint CharlesUnited StatesUnknown status
Artemis Institute for Clinical Research
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San DiegoUnited StatesUnknown status
California Neuroscience Research
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Sherman OaksUnited StatesUnknown status
Bio Behavioral Health
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Toms RiverUnited StatesUnknown status
Pacific Clinical Research Management Group
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UplandUnited StatesUnknown status
Adams Clinical Watertown
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WatertownUnited StatesUnknown status
Vitalix Clinical, Inc
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WorcesterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.