An Open-label Study of Azetukalner in Bipolar I or II Depression (X-CEED-OLE) (NCT07217860) | Clinical Trial Compass
By InvitationPhase 3
An Open-label Study of Azetukalner in Bipolar I or II Depression (X-CEED-OLE)
United States400 participantsStarted 2025-10-30
Plain-language summary
X-CEED-OLE is a Phase 3, multicenter, open-label study to evaluate the long-term safety, tolerability, and efficacy of azetukalner in adult participants who successfully completed an antecendent Phase 3 azetukalner bipolar depression study.
Who can participate
Age range18 Years – 75 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Participant successfully completed the treatment period in a Phase 3 antecedent study evaluating azetukalner in participants with bipolar depression.
* Participant provides written informed consent to participate in the study, is able to understand the procedures and study requirements, and agrees to abide by them.
* Participant is willing to comply with the contraception requirements.
Exclusion Criteria:
* Participant met any of the withdrawal criteria, discontinued study drug early, or was terminated early from an antecedent study.
* Participant had any protocol deviations in an antecedent study that, in the opinion of the investigator, would preclude participation in this study.
* Participant has any medical condition, personal circumstance, or ongoing AE (from an antecedent study) that, in the opinion of the investigator, exposes the participant to unacceptable risk by participating in the study or prevents adherence to the protocol.
* Participant is pregnant, breastfeeding, or planning to become pregnant.
* Participant is planning to enter a clinical study with a different investigational drug or planning to use any experimental device for the treatment of any medical condition during the study or within 28 days after completion of this study.
* Participant is judged by the investigator to have a significant risk for self-harm or suicidal behavior during their participation in the study or is considered to be an imminent danger to themself or oth…
What they're measuring
1
Severity and frequency of treatment-emergent adverse events, serious adverse events, adverse events of special interest, and events of clinical interest
Timeframe: From the start of treatment in the open-label extension study through 8 weeks after the last dose