Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:10 AM
Ignite Modification Date:
2025-12-25 @ 3:10 AM
NCT ID:
NCT01338805
Eligibility Criteria:
Inclusion Criteria:
* Completed study CBGG492A2207, cooperated with the study procedures and did not experience persistent tolerability issues
* Outpatients ≥ 45 kg (99 lb) of weight
* Patient would like to continue BGG492 treatment and the investigator believes a reasonable benefit from the long-term administration of BGG492 may be expected
* Treated with a stable dose of one or a maximum of three licensed Antiepileptic drugs (AEDs)and are known to take their medication(s) as directed
* Will make themselves available for the study period and are able to record seizures and report adverse events themselves or have a caregiver who can record and report the events
* Provided written informed consent before any extension assessment is performed
Exclusion Criteria:
* Status epilepticus or seizure clusters occurring during study CBGG492A2207 or in the period between the end of study the double blind study and the start of study CBGG492A2212 for patients experiencing a treatment gap
* Have been treated with:
* Felbamate, unless treatment has been continuous for ≥ 2 years
* Vigabatrin during the 26 weeks prior to the first dose of open-label medication in the extension study
* Monoamine oxidase (MAO) inhibitors, tricyclic-antidepressants and narcotic analgesics
* L-Dopa formulations
* Use of concomitant medication that are potential inhibitors of Organic anion-transporting polypeptide (OATP) transporters
* No physical examination changes suggestive of progressive neurological changes during Study CBGG492A2207
* Used another investigational drug (other than BGG492) either at the time of enrollment in this extension study or within 5 half-lives prior to enrollment in this extension study
* History of hypersensitivity to the study drug or to drugs of similar chemical classes (e.g. sulfonamides) or had multiple drug allergies or one or more severe drug reactions to an Antiepileptic drugs (AEDs), including dermatological reactions
* Pregnant or nursing (lactating) women
Other protocol-defined inclusion/exclusion criteria may apply
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
66 Years
Study:
NCT01338805
Study Brief:
Protocol Section:
NCT01338805