An Open-label Study of Azetukalner in Bipolar I or II Depression (X-CEED-OLE)

Prior treatment

• Participant met any of the withdrawal criteria, discontinued study drug early, or was terminated early from an antecedent study.
• 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.

Other illness

• 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.

Other

• Participant had any protocol deviations in an antecedent study that, in the opinion of the investigator, would preclude participation in this study.
• Participant is pregnant, breastfeeding, or planning to become pregnant.
• 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 others.

• 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.