A Study to Evaluate the Safety, Efficacy, and PK of ONO-2017 in Japanese Patients With POS 2 to 17 Year Olds

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age2-17
SponsorOno Pharmaceutical Co., Ltd.

About this trial

Primary objective: To evaluate the safety and tolerability of cenobamate in Japanese pediatric subjects 2-17 years of age with partial-onset (focal) seizures

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Japanese male or female patients aged 2 to under 18 years at the time of informed consent.

Patients diagnosed with epilepsy as having POS with uncontrolled seizures at least 6 months prior to informed consent, regardless of the presence or absence of secondarily generalized seizures.

Patients who have had POS at least once in 4 weeks before registration. Seizure information can be obtained from the participant's own retrospective patient epilepsy diary, etc.

Participants must have been treated with 1 to 3 ASMs at stable doses for at least 2 months before registration.

Disqualifiers

Patients with a history of status epilepticus requiring hospitalization within 3 months before registration.

Patients with a history of non-epileptic psychogenic seizures.

Patients with simple partial seizures without motor symptoms or idiopathic generalized epilepsy.

Patients diagnosed with Lennox-Gastaut syndrome.

Trial design

Design model

Single group

Treatments tested in this trial

  • Cenobamate (tablet) for 12 to < 18 year olds

    Drug

    The tablet form of ONO-2017 will be initiated at a dose of 12.5 mg once daily and titrated in the specified method to a target dose of 200 mg per day. The daily dose may be increased/reduced as appropriate according to symptoms within the range not exceeding 400 mg. In addition, depending on clinical response and tolerability, dose titration may be stopped at a dose of ≥ 50 mg per day to establish the maintenance dose. In principle, all doses should be taken with an appropriate amount of water in the morning. The dosage form for the doses will be selected by the principal investigator or designee. ONO-2017 can be treated until ONO-2017 is market approved, enters the market, and becomes available for supply to the study site.

  • Cenobamate (syrup) for 2 to < 18 year olds

    Drug

    The syrup form of ONO-2017 will be administered at a dose equivalent to that for 12-18 year olds on a body weight basis

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: 2 to < 18 year oldsExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Adverse events and adverse drug reactions

Time frame
1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

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