Evaluation of Onfi Conversion Therapy Replacing Clonazepam in Patients With Medically Refractory Epilepsy



Status:Active, not recruiting
Conditions:Neurology
Therapuetic Areas:Neurology
Healthy:No
Age Range:18 - 70
Updated:4/21/2016
Start Date:February 2013
End Date:September 2016

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Evaluation of Onfi Conversion Therapy Replacing Clonazepam in Patients With Medically Refractory Epilepsy: Efficacy, Tolerability, Dosing Equivalence, and Retention Rate

The purpose of the study is to examine the clinical safety, tolerability, and efficacy of
clobazam (Onfi) when it replaces the pre-existing clonazepam therapy in patients with
refractory epilepsy.

The study is designed to answer frequently asked questions when clinicians replace existing
1,4-benzodiazepine to Onfi, as follows:

1. What should be the optimal equivalent doses for conversion?

2. How quickly should it be converted?

3. Would there be significant improvement of seizure control?

4. Should we expect difference in tolerability? If so, what are common adverse events?

5. Would the tolerance to the therapeutic effect differ with Onfi after conversion?

Inclusion Criteria:

- Subject has a confirmed diagnosis of medically refractory epilepsy with or without
secondary generalization for at least 12 months prior to the initial study visit.

- Currently taking stable dosing regimen of clonazepam (0.5-4mg daily) for seizure
control.

- Takes at least one additional Anti-epileptic drug besides benzodiazepine.

- Age 18-70 years, inclusive.

- In opinion of investigator, can be safely treated with Onfi.

- Minimum of 2 seizures, but no more than 24 complex partial or generalized seizures,
during the 8-week baseline period prior to study entry.

- Able to communicate effectively with study personnel and considered reliable, able,
willing, and cooperative with regard to complying with protocol-defined requirements,
including completion of study diary.

Exclusion Criteria:

- Clinically relevant current illness or history of that may interfere with the
subject's ability to complete the study as determined by the investigator.

- History of status epilepticus within 6 months prior to the initial study visit.

- History of suicidal attempts or suicidal ideation within 12 months of initial visit.
We found this trial at
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Phoenix, Arizona 85006
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Phoenix, AZ
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