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Observational Study in Infants Who Are Prescribed Treatment With Keppra® (Levetiracetam) Oral Solution

Completed
Conditions
Epilepsy
Registration Number
NCT01210690
Lead Sponsor
UCB Pharma
Brief Summary

The purpose of this observational study is to broaden the knowledge of the known safety and efficacy profile of Keppra® (Levetiracetam) oral solution in epileptic infants younger than 12 months when treated according to routine clinical practice. Their data will be collected until they reach the age of 13 months.

Detailed Description

This non-interventional sentinel sites post-authorization safety study (PASS) aims to collect additional data on use of Keppra® (Levetiracetam) oral solution in clinical practice, and on efficacy and safety of Keppra® (Levetiracetam) in infants younger than12 months. Epileptic patients between the age of 1 month and 11 months inclusive can be invited for participation to the non-interventional sentinel sites PASS, after the physician has decided to initiate therapy with Keppra® (Levetiracetam) oral solution (100 mg/ml bottle) and patient has so far been treated with Keppra® (Levetiracetam) for no longer than 10 days. The patients will be followed and their data will be collected until they reach the age of 13 months.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
101
Inclusion Criteria
  • diagnosis of epilepsy
  • being treated with Keppra® Oral Solution
  • aged between 1 month and 11 months inclusive at study baseline
Exclusion Criteria
  • none

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Treatment-Emergent Adverse Events (TEAEs) From Baseline Through Safety Follow-up VisitFrom Baseline through the Safety Follow-up Visit (maximum Treatment Period is 12 months plus 2-week safety follow-up)

Number of patients with any Treatment-Emergent Adverse Events (TEAEs) as reported by the patient's parent and/or caregiver or observed by the treating physician during the study (maximum Treatment Period is 12 months plus 2-week safety follow-up).

Secondary Outcome Measures
NameTimeMethod
Presence of Deviation From the Normal Milestones of Psychomotor Development From Baseline to the Last Treatment VisitFrom Baseline to the last Treatment Visit (maximum 12 months)

Number of patients with presence of deviation from the normal milestones of psychomotor development during the Treatment Period (maximum 12 months). The treating physician evaluated at each visit, as part of standard clinical practice, the psychomotor development of the patient. The evaluation of the patient's psychomotor development was categorized by the motor development, the social development and the language development.

Incidence of Overall Serious Treatment-Emergent Adverse Events (TEAEs) From Baseline Through the Safety Follow-upFrom Baseline through the Safety Follow-up Visit (maximum Treatment Period is 12 months plus 2-weeks safety follow-up)

Number of patients with any serious Treatment-Emergent Adverse Events (TEAEs) during the study (maximum Treatment Period is 12 months plus 2-week safety follow-up).

Number of Patients Who Withdraw Due to Lack or Loss of Efficacy During the Treatment PeriodFrom Baseline through the last Treatment Visit (maximum 12 months)

Number of patients who withdraw due to lack or loss of efficacy during the Treatment Period (maximum 12 months).

Incidence of Treatment-Emergent Adverse Events (TEAEs) Leading to Temporary or Permanent Discontinuation of Keppra® (Levetiracetam) From Baseline Through the Last VisitFrom Baseline through the last Treatment Visit (maximum 12 months)

Number of patients with any Treatment-Emergent Adverse Events (TEAEs) leading to temporary or permanent discontinuation of Keppra® (Levetiracetam) during the Treatment Period (maximum 12 months).

Mean Change From Baseline in Standardized Body Weight Scores at the Safety Follow-up VisitFrom Baseline to the safety follow-up visit (maximum treatment period is 12 months plus 2-week safety follow-up)

For each visit, body weight was measured and standardization for gender and age was performed based on WHO growth charts to obtain z-scores. For this outcome measure, the mean of the differences of individual body weight z-scores from Safety Follow-up Visit to Baseline was determined.

Mean Change From Baseline in Standardized Head Circumference Scores at the Safety Follow-up VisitFrom Baseline to the Safety Follow-up Visit (maximum Treatment Period is 12 months plus 2-week safety follow-up)

For each visit, head circumference was measured and age standardization was performed based on WHO growth charts to obtain z-scores. For this outcome measure, the difference of head circumference z-scores from Safety Follow-up Visit to Baseline was determined and averaged across the study population.

Number of Patients With Abnormalities Noted During Neurological Examination From Baseline to the Last Treatment VisitFrom Baseline to the last Treatment Visit (maximum 12 months)

The Number of Patients With Abnormalities Noted During Neurological Examination cannot be given because abnormality frequencies were only determined for single parameters of the neurological examination and therefore a subject might have been counted several times.

Global Evaluation Scale of Epilepsy Severity (GES)From Baseline to the last Treatment Visit (maximum time frame is 12 months)

Global evaluation scale of epilepsy severity (GES): physician's assessment of the change from Baseline of the epilepsy severity at the last Treatment Visit (maximum 12 months). The GES is a 7-point scale that assesses change in the severity of the patient's illness. The GES is a 7-point scale with the following options:

7=Marked improvement

6=Moderate improvement

5=Slight improvement

4=No Change

3=Slight worsening

2=Moderate worsening

1=Marked worsening

As a variant of this variable, a 3-class variable was derived as follows

* "Marked improvement," "Moderate improvement," and "Slight improvement" were defined as "Improved."

* "No change" was defined as "Stable."

* "Slight worsening," "Moderate worsening," and "Marked worsening" were defined as "Worsened."

Mean Change From Baseline in Standardized Body Length Scores at the Safety Follow-up VisitFrom Baseline to the Safety Follow-up Visit (maximum Treatment Period is 12 months plus 2-week safety follow-up)

For each visit, body length was measured and age standardization was performed based on WHO growth charts to obtain z-scores. For this outcome measure, the difference of body length z-scores from Safety Follow-up Visit to Baseline was determined and averaged across the study population.

Number of Patients With Abnormalities Noted During Physical Examination From Baseline to the Last Treatment VisitFrom Baseline to the last Treatment Visit (maximum 12 months)

Number of patients with abnormalities noted during physical examination over the Treatment Period (maximum 12 months). Any abnormal findings during the physical examination during the study were reported as Adverse Events (AEs).

The Number of Patients With Abnormalities Noted During Physical Examination From Baseline to the Last Treatment Visit cannot be given because abnormalities at Screening are listed only and worsening after Screening were handled as AEs and tabulated along with the other AEs.

Global Evaluation Scale of the Psychomotor Development (GES)From Baseline to the last Treatment Visit (maximum 12 months)

Global evaluation scale of the psychomotor development (GES): physician's assessment of the change from Baseline in the psychomotor development at the last Treatment Visit (maximum timeframe is 12 months). The GES is a 7-point scale with the following options:

7=Marked improvement

6=Moderate improvement

5=Slight improvement

4=No Change

3=Slight worsening

2=Moderate worsening

1=Marked worsening

As a variant of this variable, a 3-class variable was derived as follows

* "Marked improvement," "Moderate improvement," and "Slight improvement" were defined as "Improved."

* "No change" was defined as "Stable."

* "Slight worsening," "Moderate worsening," and "Marked worsening" were defined as "Worsened."

Trial Locations

Locations (27)

065

🇵🇱

Gdansk, Poland

032

🇮🇹

Milano, Italy

027

🇩🇪

Berlin, Germany

022

🇩🇪

Muenster, Germany

012

🇫🇷

Amiens, France

057

🇬🇧

Birmingham, United Kingdom

063

🇵🇱

Szczecin, Poland

071

🇬🇷

Patras, Greece

031

🇮🇹

Calambrone, Italy

035

🇮🇹

Verona, Italy

045

🇪🇸

Madrid, Spain

024

🇩🇪

Bielefeld, Germany

043

🇪🇸

Barcelona, Spain

023

🇩🇪

Kiel, Germany

044

🇪🇸

Madrid, Spain

026

🇩🇪

Heidelberg, Germany

072

🇬🇷

Athens, Greece

037

🇮🇹

Bologna, Italy

021

🇩🇪

Kehl Kork, Germany

034

🇮🇹

Roma, Italy

010

🇫🇷

Bron, France

011

🇫🇷

Paris, France

051

🇬🇧

London, United Kingdom

046

🇪🇸

Murcia, Spain

052

🇬🇧

Liverpool, United Kingdom

064

🇵🇱

Lodz, Poland

062

🇵🇱

Warszawa, Poland

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