Perampanel for Treatment of Adults With Refractory Focal Epilepsy : a Pilot Study.

Stopped early · Phase 4

Conditions studied: Epilepsy

In brief

The goal of the present study is to evaluate ("screen") a large number (12) of different dual therapies of perampanel + another AED ("PMP+") for a large, 75-100% seizure frequency reduction. The design of the study will differ from usual AED studies. The study will be (i) open label, with (ii) a small n per group, n=6, with (iii) outcome measures a 'blockbuster effect': (a) ≥75 seizure frequency reduction; and (b) seizure freedom.

Key facts

Study ID

NCT02727101

Run by

Mid-Atlantic Epilepsy and Sleep Center, LLC

People needed

8

Starts

2015-11-01

Expected to finish

2017-07-01

Last updated by the study team

2017-08-29

Who can join

Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Age 18-65
• Stable focal epilepsy, with partial complex seizures including partial complex seizures with or without secondary generalization, partial simple seizures with a clear motor component with or without secondary generalization, and partial simple seizures with secondary generalization.
• Stable dose for at least 30 days of the chosen background AED dose
• Epilepsy duration for > 2 years
• Past/current treatment with > 4 AEDs. Vagal nerve stimulator treatment will be allowed and will not count as an AED. VNS setting must be stable for 3 months prior to enrollment.
• Seizure frequency of ≥1/month

You may not qualify if…

• Primary generalized epilepsy
• Simple partial seizures without motor components or secondary generalization
• Non-epileptic seizures
• Progressive neurological disease including growing neoplasm, CNS degenerative disorders including Alzheimer's disease, other forms of dementia
• Any systemic illness or unstable medical condition that might pose additional risk, including renal or liver disease, clinically uncontrolled cardiac disease, other unstable metabolic or endocrine disturbances, and active systemic cancer
• Change in the dose of any Antiepileptic Drug within 30 days prior to enrollment
• Psychosis within six months of enrollment.
• Active drug or alcohol dependence or any other factors that, in the opinion of the site investigators would interfere with adherence to study requirements;
• Pregnancy
• Use of any CNS-active investigational drugs within 3 months of enrollment.
• Inability or unwillingness of subject or legal guardian/representative to give written informed consent.

Where it is running

• MidAtlantic Epilepsy and Sleep Center — Bethesda, Maryland, United States

Full record on ClinicalTrials.gov

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