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NCT07172516Active, not recruitingPhase 3

A Randomized Study of Azetukalner Versus Placebo in Depressive Episodes Associated With Bipolar I or II Disorder (Bipolar Depression)

A Phase 3, Randomized, Double-blind, Placebo-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Azetukalner in Depressive Episodes Associated With Bipolar I or II Disorder (Bipolar Depression)

Source: ClinicalTrials.gov · Last updated 13 Oct 2026

Brief summary (registry, in English)

X-CEED is a Phase 3, multicenter, randomized, double-blind, placebo-controlled study to evaluate the efficacy and safety of azetukalner in adult participants diagnosed with bipolar I or II disorder who are currently in a depressive episode (bipolar depression).

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
400 (estimated)
First submitted
8 Sept 2025
Start date
8 Aug 2025
Primary completion date
Jun 2028
Lead sponsor
Xenon Pharmaceuticals Inc.
NCT number
NCT07172516

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 400
  • From 8 Aug 2025 to the primary completion date, Jun 2028
  • 44 sites in 4 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 substance use disorder (excluding tobacco) within the 6 months prior to screening visit.
  • Participant has a symptomatic eating disorder within the 12 months prior to screening visit.
  • Participant has been hospitalized for mania within the 30 days prior to screening visit.
  • Participant is considered treatment-resistant in the current bipolar depressive episode, defined as having treatment resistance (no remission) to ≥2 different medications approved by the regional regulatory authority at an adequate dose (per regulatory approved label) and for an adequate duration (at least 6 weeks).
  • Participant has had an active suicidal plan/intent within the 6 months prior to screening, presence of suicidal behavior in the last 12 months.
  • Participant has self-injurious behavior without intent to die in the 12 months prior to screening.
  • Participant has used antidepressants, mood stabilizers, anticonvulsants, antipsychotics, or other prohibited medications within the 1 week or within a period less than 5 times the drug's half-life, whichever is longer prior to randomization.

Other illness

  • Participant has any type of major depressive disorder (MDD) diagnosis, including MDD with psychotic features, MDD with catatonia, MDD with seasonal pattern, or postpartum depression.
  • Participant has any nonbipolar psychiatric diagnosis.
  • Participants with medical conditions that may interfere with the purpose or conduct of the study.

Other

  • Participant has a Young Mania Rating Scale (YMRS) score \>12 points at screening visit or randomization.
  • Participant is pregnant, breastfeeding, or planning to become pregnant.

Who the study is looking for

  • Adults ≥18 and ≤74 years of age who experienced their first major depressive episode (MDE) prior to 50 years of age.
  • Body Mass Index (BMI) ≥18 kg/m2 and ≤40 kg/m2.
  • Meets the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR) criteria for bipolar I or II disorder and is currently in a MDE, confirmed using the Mini International Neuropsychiatric Interview (MINI).
  • Current MDE must has a duration of ≥4 weeks and ≤12 months.

Age in the registry: 18 years to 74 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (44)

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

SiteCityCountrySite status
Multiprofile Hospital for Active Treatment "Dr. Hristo Stambolski"
Coordinator of this site? Confirm its status
KazanlakBulgariaUnknown status
State Psychiatric Hospital - Lovech
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LovechBulgariaUnknown status
Saint Naum Medical Center
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SofiaBulgariaUnknown status
Diagnostic and Consulting Center XI Sofia
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SofiaBulgariaUnknown status
Diagnostics-Consultative Center Mladost M Varna OOD
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VarnaBulgariaUnknown status
Universitätsklinikum Carl Gustav Carus, TU Dresden - Klinik und Poliklinik für Psychiatrie
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DresdenGermanyUnknown status
University Hospital Munster
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MünsterGermanyUnknown status
Instituto de Psiquiatría y Salud Mental Hospital General Universitario Gregorio Marañón
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MadridSpainUnknown status
Hospital Universitari Son Espases
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Palma de MallorcaSpainUnknown status
HU. Álvaro Cunqueiro
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PontevedraSpainUnknown status
Lehigh Center for Clinical Research
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AllentownUnited StatesUnknown status
Elevate Synapsis, LLC
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AtascocitaUnited StatesUnknown status
Synexus Clinical Research, Inc.
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AtlantaUnited StatesUnknown status
Atlanta Center for Medical Research
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AtlantaUnited StatesUnknown status
Clinical Innovations, Inc.
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BellflowerUnited StatesUnknown status
Integrative Clinical Trials, LLC
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BrooklynUnited StatesUnknown status
Neurobehavioral Research, Inc.
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CedarhurstUnited StatesUnknown status
DelRicht Research
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CharlotteUnited StatesUnknown status
Lumina Clinical Research Center
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Cherry HillUnited StatesUnknown status
PharmaSouth Research, LLC
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Coral GablesUnited StatesUnknown status
ProScience Research Group
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Culver CityUnited StatesUnknown status
CenExel iResearch
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DecaturUnited StatesUnknown status
Revival Research Institute
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ElginUnited StatesUnknown status
Core Clinical Research
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EverettUnited StatesUnknown status
Sarkis Clinical Research
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GainesvilleUnited StatesUnknown status
Memorial Hermann Village
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HoustonUnited StatesUnknown status
Clinical Neuroscience Solutions, LLC
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JacksonvilleUnited StatesUnknown status
Redbird Clinical Research, LLC
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Las VegasUnited StatesUnknown status
Woodland International Research Group
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Little RockUnited StatesUnknown status
Clinical Neuroscience Solutions, LLC.
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MemphisUnited StatesUnknown status
Central Miami Medical Institute
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MiamiUnited StatesUnknown status
Psychiatric Care and Research Center
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O'FallonUnited StatesUnknown status
NRC Research Institute
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OrangeUnited StatesUnknown status
ATP Clinical Research
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OrangeUnited StatesUnknown status
Clinical Neuroscience Solutions, LLC
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OrlandoUnited StatesUnknown status
Advanced Quality Medical Research
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Orland ParkUnited StatesUnknown status
Clinical Innovations, Inc.
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RiversideUnited StatesUnknown status
Woodland Research Northwest
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RogersUnited StatesUnknown status
Richmond Behavioral Associates
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Staten IslandUnited StatesUnknown status
Denali Health Atlanta, LLC
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Stone MountainUnited StatesUnknown status
Bio Behavioral Health
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Toms RiverUnited StatesUnknown status
Noble Clinical Research
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TucsonUnited StatesUnknown status
Sunwise Clinical Research
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Walnut CreekUnited StatesUnknown status
Grayline Research Center
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Wichita FallsUnited StatesUnknown status

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