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

NCT00416195 | Completed Phase 2 Results

• 2 other identifiers: E2007-G000-2082006-003702-26
• Study Type: interventional
• Target: 48
• Locations: 1 country
• Sites: 2

Brief Summary

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.

Conditions

Epilepsy

Outcome Measures

Primary Outcomes (1)

• Percentage of Responders During the Maintenance Phase

  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

Secondary Outcomes (1)

• Percentage Change in the 28-day Seizure Frequency From Baseline in the Maintenance LOCF

  Baseline, Day 85 through Day 112

Study Arms (2)

E2007

EXPERIMENTAL

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).

Drug: E2007

Placebo

PLACEBO COMPARATOR

Matching placebo once daily for 16 weeks (Days 1 to 112)

Drug: Placebo

Interventions

E2007 DRUG

E2007

Placebo DRUG

Placebo

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Provide written informed consent signed by patient or legal guardian prior to entering the study or undergoing any study procedures.
• 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.
• 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.
• Are between the ages of 18 and 70 years of age, inclusive.
• Are of 40 kg (88 pounds) of weight or more.
• 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.
• Have uncontrolled partial seizures despite having been treated with at least three different AEDs (given concurrently or sequentially) for at least 2 years.
• 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.
• Are on a stable dose of the same AEDs for the 1 month prior to Visit 1.
• 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.

You may not qualify if:

• 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.
• Presence of nonmotor simple partial seizures only.
• Presence of primary generalized epilepsies or seizures, such as absences, myoclonic epilepsies, Lennox-Gastaut syndrome.
• History of status epilepticus in the past year or seizure clusters where individual seizures cannot be counted.
• 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.
• 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.
• 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.
• Patients with clinically significant ECG abnormality, including prolonged QTc (defined as QTc \>=450 msec using Fridericia's correction).
• Presence of major active psychiatric disease. Patients taking a stable dose of selective serotonin reuptake inhibitor antidepressant (except fluvoxamine) will be allowed.
• Presence of a progressive central nervous system (CNS) disease, including degenerative CNS diseases and progressive tumors.
• Have a history of psychogenic seizures in the past 2 years.
• Pregnant or lactating females.
• Have a history of drug abuse in the past 2 years and/or positive finding on urinary drug screening, other than prescribed medication.
• Have a history of alcohol abuse in the past 2 years, and/or positive finding on urinary drug screen.
• Have had multiple drug allergies (dermatological, hematological, or organ toxicity) or one or more severe drug reactions.

Sponsors & Collaborators

• Eisai Co., Ltd.: lead
• Eisai Limited: collaborator

Study Sites (2)

P. Stradina Clinical University Hospital

Riga, LV-1002, Latvia

Location

Hospital Gailezers

Riga, LV-1038, Latvia

Location

Related Publications (2)

• Bresnahan R, Hill RA, Wang J. Perampanel add-on for drug-resistant focal epilepsy. Cochrane Database Syst Rev. 2023 Apr 14;4(4):CD010961. doi: 10.1002/14651858.CD010961.pub2.

  PMID: 37059702 DERIVED

• Maguire M. Response to "Perampanel and pregnancy: Could experience be a gloomy lantern that does not even illuminate its bearer?". Epilepsy Behav. 2022 Apr;129:108654. doi: 10.1016/j.yebeh.2022.108654. Epub 2022 Mar 16. No abstract available.

  PMID: 35305920 DERIVED

MeSH Terms

Conditions

Epilepsy

Interventions

perampanel

Condition Hierarchy (Ancestors)

Brain Diseases; Central Nervous System Diseases; Nervous System Diseases

Results Point of Contact

• Title: Eisai Inc.
• Organization: Eisai Call Center

888-422-4743

Study Officials

• Julia Yang, MD, MBA

  Eisai Inc.

  STUDY DIRECTOR

Publication Agreements

• PI is Sponsor Employee: No
• Restrictive Agreement: No

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 26, 2006
• First Posted: December 27, 2006
• Study Start: December 1, 2006
• Primary Completion: February 1, 2008
• Study Completion: March 1, 2008
• Last Updated: July 11, 2014
• Results First Posted: November 22, 2012

Record last verified: 2013-08

Locations

LA (2)