An Open-label Study of XEN1101 in Epilepsy

Overview

About this study

The purpose of this study is to evaluate the long term safety, tolerability, PK, and efficacy of XEN1101 25 mg QD taken orally in subjects with Focal Onset Seizures (FOS) or Primary Generalized Tonic-Clonic Seizures (PGTCS) for the treatment of seizures for up to 3 years.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Subject must be properly informed of the nature and risks of the study and give informed consent in writing, prior to entering the study.
  • Subject must have successfully completed the DBP and have not terminated early from Study X-TOLE2, X-TOLE3, or X-ACKT, met all eligibility requirements, and had no important protocol deviations (in the opinion of the sponsor) or AEs (in the opinion of the investigator) that would preclude the subject's entry into the long-term extension study.
  • In the opinion of the investigator, the subject is able to understand verbal and written instructions and will adhere to all study schedules and requirements.
  • Subject is able to keep accurate seizure diaries.

Exclusion Criteria:

  • Subject met any of the withdrawal criteria while in Study X-TOLE2, X-TOLE3, or X-ACKT.
  • Subject has any medical condition, personal circumstance, or ongoing AE (from Study X-TOLE2, X-TOLE3, or X-ACKT) that, in the opinion of the investigator, exposes the subject to unacceptable risk by participating in the study, or prevents adherence to the protocol.
  • Subject is planning to enter a clinical study with a different investigational drug or planning to use any experimental device for treatment of epilepsy or any other medical condition during the study and until 28 days after completion of this study.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 10/22/2024. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Jacksonville, Fla.

Mayo Clinic principal investigator

William Tatum, D.O.

Contact us for the latest status

Contact information:

Alicia Kissinger-Knox Ph.D.

Kissinger-Knox.Alicia@mayo.edu

More information

Publications

Publications are currently not available