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Exploring the Safety And Tolerability of Doses of E2007 up to a Maximum of 12 mg In Patients With Refractory Partial Seizures

26 de junio de 2014 actualizado por: Eisai Co., Ltd.

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Explore the Safety And Tolerability of Doses of E2007 up to a Maximum of 12 mg In Patients With Refractory Partial Seizures

This is a randomized, double-blind, placebo-controlled, parallel group study to determine the maximum tolerated dose of E2007. Epilepsy patients with refractory partial seizures will be divided into two groups of 24 patients each. One group will be patients who take concomitant inducing AEDs (anti-epileptic drugs) and the second group will be patients who do not take concomitant inducing AEDs. In each group, 18 patients will receive E2007 (dose escalating to a maximum of 12 mg per day) and six will receive placebo.

Descripción general del estudio

Estado

Terminado

Condiciones

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Actual)

48

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Riga, Letonia, LV-1002
        • P. Stradina Clinical University Hospital
      • Riga, Letonia, LV-1038
        • Hospital Gailezers

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 70 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

INCLUSION CRITERIA

  1. Provide written informed consent signed by patient or legal guardian prior to entering the study or undergoing any study procedures.
  2. Are reliable and willing to make themselves available for the study period and are able to record seizures and report AEs themselves or have a caregiver who can record and report the events.
  3. Male and female patients will be eligible for enrollment. Females should be either of nonchildbearing potential as a result of surgery or menopause (1 year after onset), or of childbearing potential and practicing a medically acceptable method of contraception (e.g., abstinence, a barrier method plus spermicide, or intrauterine device [IUD]) for at least 1 month before Visit 1 (Screening) and for 1 month after the end of the study. They must also have a negative serum beta-human chorionic gonadotropin (B-hCG) at Screening. Those females using hormonal contraceptives must also be using an additional approved method of contraception (e.g., a barrier method plus spermicide or IUD) starting with the Baseline Phase and continuing throughout the entire study period.
  4. Are between the ages of 18 and 70 years of age, inclusive.
  5. Are of 40 kg (88 pounds) of weight or more.
  6. Have the diagnosis of epilepsy with partial seizures with or without secondarily generalized seizures according with the International League Against Epilepsy's Classification of Epileptic Seizures (1981). Diagnosis should have been established by clinical history, electroencephalogram and computed tomography/magnetic resonance imaging of the brain performed within the last 10 years and consistent with localization-related epilepsy.
  7. Have uncontrolled partial seizures despite having been treated with at least three different AEDs (given concurrently or sequentially) for at least 2 years.
  8. Have averaged at least three partial seizures per month, with no 21-day seizure-free period during the 2 months preceding randomization. This should be documented in the form of medical history, medical records, or photocopied records of the patient diary/patient chart. Simple partial seizures without motor signs will not be counted towards this inclusion criterion.
  9. Are currently being treated with one to three (maximum) marketed and approved AEDs and are known to take their medications as directed. Use of a vagal nerve stimulator is not considered an AED by this criterion.
  10. Are on a stable dose of the same AEDs for the 1 month prior to Visit 1.
  11. If using a vagal nerve stimulator, it must have been implanted at least 5 months prior to Visit 1. Stimulator parameters may not be changed for at least 1 month prior to Visit 1 or during the study. Magnet use will be allowed and documented throughout the study.

EXCLUSION CRITERIA

  1. Have participated in a study involving administration of an investigational compound within 3 months of Visit 1 (Screening), or within 5 half-lives of the previous investigational compound, whichever is longer, or who have been previously treated with E2007.
  2. Presence of nonmotor simple partial seizures only.
  3. Presence of primary generalized epilepsies or seizures, such as absences, myoclonic epilepsies, Lennox-Gastaut syndrome.
  4. History of status epilepticus in the past year or seizure clusters where individual seizures cannot be counted.
  5. Show evidence of clinically significant disease (cardiac, respiratory, gastrointestinal, renal disease, etc) that, in the opinion of the investigator, could affect either the patient's safety or the conduct of the study.
  6. Show evidence of significant, active, hepatic disease. Stable elevations of liver enzymes, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) due to concomitant medications will be allowed if they are less than 2 times the ULN.
  7. Show evidence of significant active hematological disease such as a white blood cell (WBC) count <= 2500/µL (2.50 1E+09/L), an absolute neutrophil count <= 1000/µL (1.00 1E+09/L), or a platelet count <100,000/mm^3.
  8. Patients with clinically significant ECG abnormality, including prolonged QTc (defined as QTc >=450 msec using Fridericia's correction).
  9. Presence of major active psychiatric disease. Patients taking a stable dose of selective serotonin reuptake inhibitor antidepressant (except fluvoxamine) will be allowed.
  10. Presence of a progressive central nervous system (CNS) disease, including degenerative CNS diseases and progressive tumors.
  11. Have a history of psychogenic seizures in the past 2 years.
  12. Pregnant or lactating females.
  13. Have a history of drug abuse in the past 2 years and/or positive finding on urinary drug screening, other than prescribed medication.
  14. Have a history of alcohol abuse in the past 2 years, and/or positive finding on urinary drug screen.
  15. Have had multiple drug allergies (dermatological, hematological, or organ toxicity) or one or more severe drug reactions.
  16. Allergy to lactose.
  17. Concomitant use of felbamate or use of felbamate within 2 months prior to Visit 1.
  18. Concomitant use or use within the 4 weeks prior to Visit 1 of neuroleptics, monoamine oxidase (MAO) inhibitors, barbiturates (except for seizure control indication), benzodiazepines (other than occasional intermittent use), and narcotic analgesics.
  19. Frequent need of rescue benzodiazepines (two or more times a month).

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: E2007
2 mg E2007 once daily for 2 weeks (Days 1 to 14), then 4 mg E2007 once daily for 2 weeks (Days 15 to 28), then 6 mg E2007 once daily for 2 weeks (Days 29 to 42), then 8 mg E2007 once daily for 2 weeks (Days 43 to 56), then 10 mg E2007 once daily for 2 weeks (Days 57 to 70), then 12 mg E2007 once daily for 6 weeks (Days 71 to 112).
Comparador de placebos: Placebo
Matching placebo once daily for 16 weeks (Days 1 to 112)

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Percentage of Responders During the Maintenance Phase
Periodo de tiempo: Day 85 through Day 112
A patient is a responder if she/he experiences a 50% or greater reduction in seizure frequency from the baseline phase.
Day 85 through Day 112

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Percentage Change in the 28-day Seizure Frequency From Baseline in the Maintenance LOCF
Periodo de tiempo: Baseline, Day 85 through Day 112
Baseline, Day 85 through Day 112

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Colaboradores

Investigadores

  • Director de estudio: Julia Yang, MD, MBA, Eisai Inc.

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de diciembre de 2006

Finalización primaria (Actual)

1 de febrero de 2008

Finalización del estudio (Actual)

1 de marzo de 2008

Fechas de registro del estudio

Enviado por primera vez

26 de diciembre de 2006

Primero enviado que cumplió con los criterios de control de calidad

26 de diciembre de 2006

Publicado por primera vez (Estimar)

27 de diciembre de 2006

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

11 de julio de 2014

Última actualización enviada que cumplió con los criterios de control de calidad

26 de junio de 2014

Última verificación

1 de agosto de 2013

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • E2007-G000-208
  • 2006-003702-26 (Número EudraCT)

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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