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Clinical Trials/NCT01063764
NCT01063764
Completed
Phase 3

An Open Label, Single-Arm, Multi-Center Study on the Efficacy, Safety and Pharmacokinetics of Levetiracetam in Pediatric Patients (4 to 16 Years) With Partial Seizures Despite Treatment With 1 or 2 Anti-Epileptic Drugs

UCB Japan Co. Ltd.29 sites in 1 country73 target enrollmentStarted: January 2010Last updated:

Overview

Phase
Phase 3
Status
Completed
Enrollment
73
Locations
29
Primary Endpoint
Incidence of Treatment-Emergent Adverse Events (TEAEs) During the Second Period (up to Three Years Until the Time of Approval Granted)

Overview

Brief Summary

Objective of the First Period: To evaluate the efficacy of Levetiracetam dry syrup at doses up to a maximum of 60 mg/kg/day or 3000 mg/day used as an adjunctive therapy in Japanese pediatric patients (4 to 16 years) with uncontrolled partial seizures despite treatment with 1 or 2 anti-epileptic drug(s).

Detailed Description

Objectives of the Second Period: To provide the Levetiracetam treatment to subjects who are judged by the investigators to benefit from the long-term treatment and who are willing to continuously receive this drug. To continuously evaluate the safety of the Levetiracetam long-term administration at doses ranging from 20 mg/kg/day or 1000 mg/day to 60 mg/kg/day or 3000 mg/day in subjects who completed the First Period of this study.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
4 Years to 16 Years (Child)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • The patient has partial Epilepsy and the diagnosis must be confirmed in the last 6 months
  • The patients must be on a stable 1 or 2 anti-epileptic drug(s) treatment during the 4 weeks prior to Baseline and must have at least 8 partial seizures during the 8-week prospective Baseline Period
  • Patient at the age of 4 to 16 years, and at the body weight of 11 to 82 kg

Exclusion Criteria

  • The patient has a treatable seizure etiology
  • The patient has Epilepsy secondary to a progressive cerebral disease or any other progressively neurodegenerative disease, including Rasmussen and Landau-Kleffner diseases
  • The patient has a history of status Epilepticus during the 3 months prior to Visit 1
  • The patient has a past and present history of pseudo seizures
  • The patient has a current diagnosis of Lennox-Gastaut syndrome

Arms & Interventions

Levetiracetam

Experimental

Open-label, single-arm

Intervention: Levetiracetam (Drug)

Outcomes

Primary Outcomes

Incidence of Treatment-Emergent Adverse Events (TEAEs) During the Second Period (up to Three Years Until the Time of Approval Granted)

Time Frame: During the second Period from Visit 8 (Week 22) to the end of the Follow-up Period (up to three years until the time of approval granted)

An Adverse Event (AE) is any untoward medical occurrence in a clinical investigation subject administered a pharmaceutical product which does not necessarily have a causal relationship with the pharmaceutical product. Incidence of treatment-emergent AEs is reported by the percentage of subjects with at least one treatment-emergent AE.

Change From Baseline in Partial Seizure Frequency Per Week Over the 14-weeks Treatment Period

Time Frame: From Baseline (Week 0-8) to the 14-weeks Treatment Period (First Period: 4 weeks Up-titration (Week 8-12) and 10 weeks Evaluation (Week 12-22)); Week 0-22

The change in partial seizure frequency from Baseline (B) over the Treatment Period (T) is given as a percentage reduction computed as: (B values- T values) / B values x 100. Positive values in percent reduction mean that the value decreased from Baseline during the first 14-week Period. Frequency per week of partial seizures = (Total number of partial seizures in a certain Period/number of observation days in the Period) x 7. Partial seizures can be classified into: * Simple partial seizures * Complex partial seizures * Partial seizures evolving to secondarily generalized seizures.

Secondary Outcomes

  • Partial Seizure Frequency Per Week Over the 10-weeks Evaluation Period(10-weeks Evaluation Period (Part of the first Period: Week 12 to Week 22))
  • Number of Seizure-free Subjects Over the 10-weeks Evaluation Period(10-weeks Evaluation Period (Part of the first Period: Week 12 to Week 22))
  • Incidence of Treatment-emergent Adverse Drug Reactions (ADRs) During the Second Period (up to Three Years Until the Time of Approval Granted)(During the second Period from Visit 8 (Week 22) to the end of the Follow-up Period (up to three years until the time of approval granted))
  • Percentage of Partial Seizures 50 % Responders Over the 10-weeks Evaluation Period(10-weeks Evaluation Period (Part of the first Period: Week 12 to Week 22))
  • Partial Seizure Frequency Per Week Over the 14-weeks Treatment Period(14-weeks Treatment Period (First Period: 4 weeks Up-titration (Week 8-12) and 10 weeks Evaluation (Week 12-22)))
  • Change From Baseline in Partial Seizure Frequency Per Week for the Second Period (up to Three Years From Informed Consent Until the Time of Approval Granted)(From Baseline (Week 0-8) until the time of approval granted (up to three years from date of informed consent (Week 0); without 6-weeks Withdrawal Period))
  • Change From Baseline in Partial Seizure Frequency Per Week Over the 10-week Evaluation Period(From Baseline (Week 0-8) to the 10-weeks Evaluation Period (Part of the first Period: Week 12 to Week 22))
  • Percentage of Partial Seizures 50 % Responders Over the 14-weeks Treatment Period(14-weeks Treatment Period (First Period: 4 weeks Up-titration (Week 8-12) and 10 weeks Evaluation (Week 12-22)))
  • Number of Seizure-free Subjects Over the 14-weeks Treatment Period(14-weeks Treatment Period (First Period: 4 weeks Up-titration (Week 8-12) and 10 weeks Evaluation (Week 12-22)))

Investigators

Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (29)

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