Efficacy of YKP3089 in Patients With Photosensitive Epilepsy (NCT00616148) | Clinical Trial Compass
CompletedPhase 2
Efficacy of YKP3089 in Patients With Photosensitive Epilepsy
United States11 participantsStarted 2007-08
Plain-language summary
The aim of this study is to evaluate the ability of a single oral dose of YKP3089 to abolish or clearly reduce the IPS-induced photo-paroxysmal EEG response in photosensitive epilepsy patients, and to measure the onset and duration of the effect. Several cohorts will be used, to sequentially investigate different doses.
Who can participate
Age range16 Years – 60 Years
SexALL
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Inclusion Criteria:
* Male or female age 18-60 years.
* A diagnosis and history of epilepsy for which patients are on 0-2 concomitant antiepileptic drugs.
* If the patient is taking two concomitant medications, the second drug must be levetiracetam, gabapentin or pregabalin.
* A reproducible IPS-induced photo-paroxysmal response (PPR) on EEG of at least 3 points on a frequency assessment scale (See Section 6.16) in at least one eye condition and no change of more than 3 frequencies in 2 repeated measurements recorded over the 2 months prior to study entry in at least one eye condition.
* Patients in otherwise good health (with the exception of epilepsy), as determined by the PI via the medical history, a physical examination and screening laboratory investigations.
* A body mass index (BMI) between 18 and 35.
* Able and willing to provide written informed consent to participate in the study in accordance with the ICH, GCP guidelines.
Exclusion Criteria:
* A history of non epileptic seizures (e.g. metabolic, structural or pseudo-seizures).
* Women who are pregnant or lactating.
* Women of reproductive potential who do not agree to use effective birth-control methods.
* Patients taking medications that are known substrates of CYP2B6 and CYP2C19 including but not limited to phenytoin, Phenobarbital, omeprazole, fluvoxamine and efavirenz.
* Any clinically significant laboratory abnormality which, in the opinion of the investigator, will exclude the patient from the study.
* An…
What they're measuring
1
Determine if YKP3089 will reduce or abolish the photosensitivity response as compared to placebo.