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| ID | Type | Description | Link |
|---|---|---|---|
| 2007-003517-13 | EudraCT Number |
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Keppra injection is approved in the US as adjunctive therapy in the treatment of partial onset seizures in adults with epilepsy. The objective of the current study is to assess the safety, tolerability, and pharmacokinetics, of this formulation in children aged 1 month to 4 years.
The primary objective of this study was to evaluate the safety and tolerability of levetiracetam intravenous 15-minute infusion administered every 12 hours, either as adjunctive treatment or monotherapy in children (1 month to 4 years old) with epilepsy (except status epilepticus), either after switching from the equivalent levetiracetam oral dose administration or as a new antiepileptic treatment.
The evaluation period was to be considered as one complete set of 4 pharmacokinetic (PK) samples for a maximum of 4 days;
For children already taking levetiracetam oral solution prior to entering the study, the levetiracetam intravenous (LEV IV) dose will be equivalent (mg-for-mg) to their oral dose (always in twice daily regimen) within the following dose range, calculated on the basis of their age and weight:
The first intravenous (IV) infusion was to be administered 12 hours after the last oral dose of levetiracetam.
For children not taking levetiracetam oral solution prior to entering the study, the intravenous (IV) dose will correspond to their age and weight as follows:
However, when necessary for the safety of the subject or when the investigator deemed it appropriate the levetiracetam intravenous (LEV IV) dose could be modified after one day.
Subjects were hospitalized for the duration of the levetiracetam intravenous (LEV IV) treatment.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Levetiracetam | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Levetiracetam | Drug | Intravenous 100 mg/mL, twice a day, maximum of 4 days Subjects on oral levetiracetam at study entry receive the same intravenous (IV) dosage (mg-for-mg) to their oral dose within the following dose range, calculated on the basis of their age and weight:.
For subjects not taking levetiracetam oral solution prior to entering the study, the intravenous (IV) dosage corresponded to their age and weight as follows:
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of Subjects Reporting at Least 1 Treatment-Emergent Adverse Event (TEAE) During the Treatment Period (up to 4 Days) | Treatment period (up to 4 days) |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Subjects Who Received High-dose Levetiracetam Intravenous (LEV IV) (More Than 28 mg/kg/Day for Subjects <6 Months; >40mg/kg/Day for Subjects ≥6 Months) During the Treatment Period (up to 4 Days) | Treatment period (up to 4 days) | |
| Number of Consecutive Levetiracetam Intravenous (LEV IV) Doses Received |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| UCB Clinical Trial Call Center | +1 877 822 9493 (UCB) | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| San Diego | California | United States | ||||
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 23533164 | Result | Weinstock A, Ruiz M, Gerard D, Toublanc N, Stockis A, Farooq O, Dilley D, Karmon Y, Elgie MJ, Schiemann-Delgado J. Prospective Open-Label, Single-Arm, Multicenter, Safety, Tolerability, and Pharmacokinetic Studies of Intravenous Levetiracetam in Children With Epilepsy. J Child Neurol. 2013 Nov;28(11):1423-1429. doi: 10.1177/0883073813480241. Epub 2013 Mar 26. |
| Label | URL |
|---|---|
| FDA Safety Alerts and Links | View source |
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Participant Flow refers to the Intent-to-treat (ITT) Population, consisting of all subjects who received at least 1 dose of study medication.
Subjects were recruited from sites in the United States, Belgium, Germany, France, Mexico, and Turkey. The study began in May 2008 and continued until March 2010, with the last subject's visit occurring in March of 2010.
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| ID | Title | Description |
|---|---|---|
| FG000 | Levetiracetam | Intravenous 100 mg/mL, twice a day, maximum of 4 days Subjects on oral levetiracetam at study entry receive the same intravenous (IV) dosage (mg-for-mg) to their oral dose within the following dose range, calculated on the basis of their age and weight:.
For subjects not taking levetiracetam oral solution prior to entering the study, the intravenous (IV) dosage corresponded to their age and weight as follows:
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| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| Treatment period (up to 4 days) |
| Buffalo |
| New York |
| United States |
| Philadelphia | Pennsylvania | United States |
| Nashville | Tennessee | United States |
| Fort Worth | Texas | United States |
| Richmond | Virginia | United States |
| Ghent | Belgium |
| Leuven | Belgium |
| Amiens | France |
| Lille | France |
| Paris | France |
| Vandœuvre-lès-Nancy | France |
| Heidelberg | Germany |
| Kehl | Germany |
| Kiel | Germany |
| Torreón | Coahuila | Mexico |
| Puebla City | CP | Mexico |
| Aguascalientes | Mexico |
| Guadalajara | Mexico |
| Mexico City | Mexico |
| Puebla City | Mexico |
| Ankara | Turkey (Türkiye) |
| Izmir | Turkey (Türkiye) |
| COMPLETED |
|
| NOT COMPLETED |
|
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Levetiracetam | Intravenous 100 mg/mL, twice a day, maximum of 4 days Subjects on oral levetiracetam at study entry receive the same intravenous (IV) dosage (mg-for-mg) to their oral dose within the following dose range, calculated on the basis of their age and weight:.
For subjects not taking levetiracetam oral solution prior to entering the study, the intravenous (IV) dosage corresponded to their age and weight as follows:
|
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants | Participants |
| |||||||||||||||||||||||
| Age, Continuous | Mean | Standard Deviation | years |
| ||||||||||||||||||||||
| Sex: Female, Male | Count of Participants | Participants |
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| Region of Enrollment | Number | participants |
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| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Number of Subjects Reporting at Least 1 Treatment-Emergent Adverse Event (TEAE) During the Treatment Period (up to 4 Days) | All 19 subjects enrolled in the study were included in the Intent to Treat (ITT) population and are included in this analysis. | Posted | Number | Subjects | Treatment period (up to 4 days) |
|
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| |||||||||||||||||||||||||||
| Secondary | Number of Subjects Who Received High-dose Levetiracetam Intravenous (LEV IV) (More Than 28 mg/kg/Day for Subjects <6 Months; >40mg/kg/Day for Subjects ≥6 Months) During the Treatment Period (up to 4 Days) | All 19 subjects enrolled in the study were included in the Intent to Treat (ITT) population and are included in this analysis. | Posted | Number | Subjects | Treatment period (up to 4 days) |
|
| ||||||||||||||||||||||||||||
| Secondary | Number of Consecutive Levetiracetam Intravenous (LEV IV) Doses Received | All 19 subjects enrolled in the study were included in the Intent to Treat (ITT) population and are included in this analysis. | Posted | Mean | Standard Deviation | Consecutive doses | Treatment period (up to 4 days) |
|
|
Up to 4 days
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Levetiracetam | Intravenous 100 mg/mL, twice a day, maximum of 4 days Subjects on oral levetiracetam at study entry receive the same intravenous (IV) dosage (mg-for-mg) to their oral dose within the following dose range, calculated on the basis of their age and weight:.
For subjects not taking levetiracetam oral solution prior to entering the study, the intravenous (IV) dosage corresponded to their age and weight as follows:
| 4 | 19 | 10 | 19 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| BRADYCARDIA | Cardiac disorders | MedDRA (9.0) | Non-systematic Assessment |
| |
| CARDIAC ARREST | Cardiac disorders | MedDRA (9.0) | Non-systematic Assessment |
| |
| PYREXIA | General disorders | MedDRA (9.0) | Non-systematic Assessment |
| |
| PNEUMONIA | Infections and infestations | MedDRA (9.0) | Non-systematic Assessment |
| |
| ABDOMINAL SEPSIS | Infections and infestations | MedDRA (9.0) | Non-systematic Assessment |
| |
| ELECTROCARDIOGRAM QT PROLONGED | Investigations | MedDRA (9.0) | Non-systematic Assessment |
| |
| METABOLIC ACIDOSIS | Metabolism and nutrition disorders | MedDRA (9.0) | Non-systematic Assessment |
| |
| CONVULSION | Nervous system disorders | MedDRA (9.0) | Non-systematic Assessment |
| |
| RESPIRATORY FAILURE | Respiratory, thoracic and mediastinal disorders | MedDRA (9.0) | Non-systematic Assessment |
|
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| BRADYCARDIA | Cardiac disorders | MedDRA (9.0) | Non-systematic Assessment |
| |
| EYE SWELLING | Eye disorders | MedDRA (9.0) | Non-systematic Assessment |
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| VOMITING | Gastrointestinal disorders | MedDRA (9.0) | Non-systematic Assessment |
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| PYREXIA | General disorders | MedDRA (9.0) | Non-systematic Assessment |
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| IRRITABILITY | General disorders | MedDRA (9.0) | Non-systematic Assessment |
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| PAIN | General disorders | MedDRA (9.0) | Non-systematic Assessment |
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| PUNCTURE SITE PAIN | General disorders | MedDRA (9.0) | Non-systematic Assessment |
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| PROCEDURAL PAIN | Injury, poisoning and procedural complications | MedDRA (9.0) | Non-systematic Assessment |
| |
| ELECTROENCEPHALOGRAM | Investigations | MedDRA (9.0) | Non-systematic Assessment |
| |
| SOMNOLENCE | Nervous system disorders | MedDRA (9.0) | Non-systematic Assessment |
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| DROOLING | Nervous system disorders | MedDRA (9.0) | Non-systematic Assessment |
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| MYOCLONIC EPILEPSY | Nervous system disorders | MedDRA (9.0) | Non-systematic Assessment |
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| RESTLESSNESS | Psychiatric disorders | MedDRA (9.0) | Non-systematic Assessment |
| |
| RHINORRHOEA | Respiratory, thoracic and mediastinal disorders | MedDRA (9.0) | Non-systematic Assessment |
| |
| PETECHIAE | Skin and subcutaneous tissue disorders | MedDRA (9.0) | Non-systematic Assessment |
| |
| NEURODERMATITIS | Skin and subcutaneous tissue disorders | MedDRA (9.0) | Non-systematic Assessment |
| |
| HYPOTENSION | Vascular disorders | MedDRA (9.0) | Non-systematic Assessment |
|
UCB has > 60 days but <= 180 days to review results communications prior to public release and may delete information that is confidential and compromises ongoing studies or is considered proprietary. This restriction is not intended to compromise the objective scientific integrity of the manuscript, it being understood that results shall be published regardless of outcome.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| UCB Clinical Trial Call Center | UCB | +1 877 822 9493 |
| ID | Term |
|---|---|
| D004827 | Epilepsy |
| ID | Term |
|---|---|
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
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| ID | Term |
|---|---|
| D000077287 | Levetiracetam |
| ID | Term |
|---|---|
| D000081 | Acetamides |
| D000577 | Amides |
| D009930 | Organic Chemicals |
| D000085 | Acetates |
| D000144 | Acids, Acyclic |
| D002264 | Carboxylic Acids |
| D011760 | Pyrrolidinones |
| D011759 | Pyrrolidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
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| Belgium |
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| Turkey |
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| Germany |
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