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Antiepileptic

Levetiracetam for Neonatal Seizures (NEOLEV3 Trial)

Phase 2
Recruiting
Led By Jeff J Gold, M.D. PhD
Research Sponsored by University of California, San Diego
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 8 years
Awards & highlights

NEOLEV3 Trial Summary

This trial investigates the best dose of Levetiracetam to treat newborns' seizures. It includes a randomized control treatment component and will assess a higher dose of LEV than previously used.

Who is the study for?
This trial is for term neonates (newborns aged less than 28 days) weighing over 2200g, with a variety of seizure causes. It's not for those with severe seizures or correctable metabolic issues like low blood sugar/calcium, or kidney failure.Check my eligibility
What is being tested?
The study tests the safest high dose of Levetiracetam (LEV) for treating newborn seizures compared to Phenobarbital Sodium (PHB). Babies will be monitored and randomly given either LEV or PHB if their seizures continue after an initial LEV dose.See study design
What are the potential side effects?
Possible side effects include sleepiness, changes in behavior, digestive discomfort, and potential allergic reactions. The exact side effects in newborns are being studied as part of this trial.

NEOLEV3 Trial Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~8 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and 8 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Levetiracetam
Secondary outcome measures
Adverse event rates
Estimate of efficacy of higher dose LEV
Levetiracetam CL
+4 more

NEOLEV3 Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Dose escalation with LEVExperimental Treatment1 Intervention
Additional LEV at a higher dose (30 mg/kg, 60 mg/kg, or 90 mg/kg depending on the stage of the study).
Group II: Standard of care PhenobarbitalActive Control1 Intervention
Treatment with Phenobarbital 20mg/kg IV and if needed a further 20mg/kg totalling 40mg/kg

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Levetiracetam, a common treatment for neonatal seizures, works by modulating neurotransmitter release through binding to the synaptic vesicle protein SV2A. This action helps stabilize neuronal activity and prevent seizures. This mechanism is particularly important for neonatal seizure patients because their developing brains are highly susceptible to excitatory imbalances, which can lead to frequent and severe seizures. By targeting the neurotransmitter release process, Levetiracetam offers a targeted approach to reduce seizure activity with potentially fewer side effects compared to traditional anticonvulsants like phenobarbital, which work by enhancing inhibitory neurotransmission broadly and can have more sedative effects.

Find a Location

Who is running the clinical trial?

Middlemore Hospital, New ZealandOTHER
5 Previous Clinical Trials
6,062 Total Patients Enrolled
Sharp Mary Birch Hospital for Women & NewbornsOTHER
12 Previous Clinical Trials
6,602 Total Patients Enrolled
University of Auckland, New ZealandOTHER
71 Previous Clinical Trials
17,190 Total Patients Enrolled

Media Library

Levetiracetam Injection (Antiepileptic) Clinical Trial Eligibility Overview. Trial Name: NCT05610085 — Phase 2
Hypoxic-Ischemic Encephalopathy Research Study Groups: Standard of care Phenobarbital, Dose escalation with LEV
Hypoxic-Ischemic Encephalopathy Clinical Trial 2023: Levetiracetam Injection Highlights & Side Effects. Trial Name: NCT05610085 — Phase 2
Levetiracetam Injection (Antiepileptic) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05610085 — Phase 2
~82 spots leftby Jul 2026