A Dose Escalation Study of Levetiracetam in the Treatment of Neonatal Seizures

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
AgeUp to 1
SponsorUniversity of California, San Diego

About this trial

The main purpose of this study is to determine the maximum safe tolerated dose of LEV in the treatment of neonatal seizures. Our hypothesis is that optimal dosing of Levetiracetam (LEV) to treat neonatal seizures is significantly greater than 60mg/kg. This study will be an open label dose-escalation, preliminary safety and efficacy study. There will be a randomized control treatment component. Infants recognized as having neonatal seizures or as being at risk of developing seizures will be recruited and started on continuous video EEG monitoring (CEEG). Eligibility will be confirmed and consent will be obtained. In the first 2 phases of the study, neurologists will identify neonates with mild-moderate seizure burden (less than 8 minutes cumulative seizure activity per hour), appropriate for study with LEV, and exclude patients with higher seizure burden where treatment with PHB is more appropriate. Phase 3 of the dose escalation will only proceed if additional efficacy of LEV has been demonstrated in phases 1 and 2. In Phase 3 we will recruit neonates with seizures of greater severity up to 20 minute seizure burden/hour. This will make the final results of study more generalizable.

If seizures are confirmed, enrolled subjects will receive 60mg/kg of LEV. Subjects whose seizures persist or recur 15 minutes after the first infusion is complete, subjects will then be randomized in the dose escalation study. Patients in the dose escalation study will be randomly assigned to receive either higher dose LEV or treatment with the control drug PHB in a 3:1 allocation ratio, stratified by site.

Funding Source- FDA OOPD

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

at risk for seizures or suspected to be having seizures;

all seizure aetiologies except correctable metabolic abnormalities such as hypoglycaemia and hypocalcaemia;

Term neonates (corrected gestational age between 35 and 44 weeks, postnatal age less than 28 days);

weight > 2200g.

Disqualifiers

Cumulative seizure burden of 8 minutes/ hour or more in phases 1 and 2, Cumulative seizure burden of 20 minutes/hour or more in phase 3;

Renal failure defined as anuria in the first 24 hours of life;

Subjects in whom death seems imminent;

Seizures caused by correctable metabolic abnormality, such as hypocalcaemia, hypoglycaemia.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Levetiracetam Injection

    Drug

    Neonates will be treated with intravenous levetiracetam 60mg/kg for first line management of seizures, and if seizures persist will be randomized to receive higher dose Levetiracetam or standard of care phenobarbital

  • Phenobarbital Sodium Injection

    Drug

    Standard of care for neonatal seizures

Treatment groups

133 Participants
are divided into 2 treatment groups
Group A: Dose escalation with LEVExperimental treatment 1 intervention
Group B: Standard of care PhenobarbitalActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

The primary endpoint is the maximum safe and tolerated dose of Levetiracetam

A continual reassessment method will be used to determine the maximal safe and tolerated dose

Time frame
4 years

Secondary outcomes

1

Levetiracetam CL

Population pharmacokinetic parameters for LEV Clearance (CL)will be calculated

Time frame
4 years
2

Levetiracetam Vd

Population pharmacokinetic parameters for LEV Volume of distribution (Vd) will be calculated

Time frame
4 years
3

Adverse event rates

Rates of adverse events seen with high dose LEV treatment will be reported and compared to rates seen in PHB control arm.

Time frame
4 years
4

Long-term outcome

Rates of adverse long-term outcome ( Death or Disability at 24 months) will be compared between treatment arms

Time frame
8 years

Other outcomes

Sponsors and contacts

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University of California, San Diego

Lead sponsor

University of Minnesota

Collaborator

Rady Children's Hospital, San Diego

Collaborator

Auckland City Hospital

Collaborator

University of Auckland, New Zealand

Collaborator

Middlemore Hospital, New Zealand

Collaborator

Waikato Hospital

Collaborator