A Safety, Efficacy and Tolerability Trial of Pregabalin as Add-On Treatment in Pediatric and Adult Subjects With Primary Generalized Tonic-Clonic (i.e., Grand Mal) Seizures.



Status:Completed
Conditions:Neurology
Therapuetic Areas:Neurology
Healthy:No
Age Range:5 - 65
Updated:3/17/2019
Start Date:April 3, 2013
End Date:February 20, 2019

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A RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP, MULTI-CENTER TRIAL OF PREGABALIN AS ADJUNCTIVE THERAPY IN PEDIATRIC AND ADULT SUBJECTS WITH PRIMARY GENERALIZED TONIC-CLONIC SEIZURES - PROTOCOL A0081105

The study is designed to evaluate the safety, tolerability and efficacy of two doses of
pregabalin as add-on treatment in pediatric and adult subjects with Primary Generalized
Tonic-Clonic (PGTC) seizures as compared to placebo. It is hypothesized that both doses of
pregabalin will demonstrated superior efficacy when compared to placebo by reducing PGTC
seizure frequency and that pregabalin will be safe and well tolerated.


Inclusion Criteria:

- Seizures classified as Primary Generalized Tonic Clonic Seizures

- Must have at least 1 PGTC seizure in the 8 weeks prior to screening

- Must have a minimum of 3 PGTC seizures during the 8-week baseline phase and at least 1
PGTC in each 4-week period of the baseline phase

- Currently receiving adequate and stable dosage of 1 to 3 anti-epileptic treatments
(stable within 28 days of screening)

- Signed informed consent and assent if a minor

- Ability to comply with daily seizure and dosing diary requirements and all study
procedures

Exclusion Criteria:

- A current diagnosis of febrile seizures, or seizures related to an ongoing acute
medical illness

- Focal seizures (simple partial, complex partial, or partial becoming secondarily
generalized)

- Status Epilepticus within 1 year prior to screening

- Lennox-Gastaut syndrome, infantile spasms, Benign Epilepsy with Centrotemporal Spikes
(BECTS) and Dravet syndrome

- Seizures related to drugs, alcohol, or acute medical illness

- Any change in anti-epileptic treatment regimen (type of medication or dose; VNS
alteration) within 28 days of the screening visit or during the baseline phase

- Progressive or potentially progressive structural CNS lesion or a progressive
encephalopathy.

- Progressive inborn errors of metabolism.
We found this trial at
13
sites
7485 Sandlake Commons Blvd.
Orlando, Florida 32835
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Canton, OH
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Hoffman Estates, Illinois 60169
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1786 Moon Lake Boulevard
Hoffman Estates, Illinois 60169
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1555 North Barrington Road
Hoffman Estates, Illinois 60169
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Honolulu, Hawaii 96817
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Honolulu, HI
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Loxahatchee Groves, Florida 33470
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Loxahatchee Groves, FL
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Orlando, FL
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Port Charlotte, Florida 33952
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Port Charlotte, FL
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Renton, Washington 98057
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Renton, WA
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San Antonio, Texas 78258
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San Antonio, TX
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Santa Fe,
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Temple, TX
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