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Not yet recruiting NCT07723963

A Study to Evaluate the Safety and Efficacy of JZP926 Capsule for the Treatment of Juvenile Myoclonic Epilepsy

Phase II / Phase III Interventional Juvenile Myoclonic Epilepsy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: JZP926 capsule, Placebo.
Who it may be relevant to
Registry conditions: Juvenile Myoclonic Epilepsy. Basic parameters: from 10 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Phase 2/3, Multicenter, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Safety and Efficacy of JZP926 in Participants Aged 10 Years and Older for the Treatment of Juvenile Myoclonic Epilepsy

Overview

This study is being conducted to evaluate the safety and efficacy of JZP926 capsule in participants with Juvenile Myoclonic Epilepsy (JME).

Detailed description

This Phase 2/3 multicenter, randomized, placebo-controlled, double-blind study will evaluate the safety and efficacy of JZP926 capsule in participants aged ≥ 10 years with Juvenile Myoclonic Epilepsy (JME). The study will assess the efficacy of JZP926 capsule as an adjunctive treatment in reducing the frequency of myoclonic seizure days when compared with placebo, as well as the effect of JZP926 capsule on non-seizure endpoints.

Interventions

  • Drug JZP926 capsule
    Oral administration BID according to body weight
  • Drug Placebo
    Oral administration BID according to body weight

Primary outcome measures

  • Change from baseline in myoclonic seizure days per 28 days (Part A and Part B) [Time frame: Baseline up to end of 16 weeks treatment period]
Secondary outcome measures (9)
  • Patient and Caregiver Global Impression of Change in Usual Daily Activities (P/CaGI-C UDA) (Part A and Part B) [Time frame: Week 16]
  • Proportion of participants who achieve ≥ 50% and ≥ 75% reduction from baseline in myoclonic seizure days (Part A and Part B) [Time frame: Baseline up to end of 16 weeks treatment period]
  • Change from baseline in days with any seizure type per 28 days (Part A and Part B) [Time frame: Baseline up to end of 16 weeks treatment period]
  • Number of days with fewer myoclonic seizures than participant average prior to entering the study per 28 days (Part A and Part B) [Time frame: Baseline up to end of 16 weeks treatment period]
  • Percent change from baseline (historical + prospective) in generalized tonic-clonic (GTC) seizure frequency (Part A and Part B) [Time frame: Baseline up to end of 16 weeks treatment period]
  • Number of participants reporting treatment-emergent adverse events (Part A and Part B) [Time frame: Baseline up to end of 16 weeks treatment period]
  • Mean plasma concentration for CBD [Time frame: Baseline up to end of 16 weeks treatment period]
  • Mean plasma concentration of metabolite 7-OH-CBD [Time frame: Baseline up to end of 16 weeks treatment period]
  • Mean plasma concentration of metabolite 7-COOH-CBD [Time frame: Baseline up to end of 16 weeks treatment period]

Eligibility criteria

Inclusion criteria

Participants are eligible to be included in the study only if all of the following criteria apply:

  • Is ≥ 10 years of age at the time of screening.
  • Has a diagnosis of JME per ILAE criteria as specified in the protocol.
  • Has at least 4 myoclonic seizure days per 28 days historical seizure frequency.

Exclusion criteria

Participants are excluded from the study if any of the following criteria apply:

  • Presence of seizure types other than GTC, myoclonic, and absence seizures.
  • If historical MRI has been performed, participant's MRI reveals a cause of epilepsy other than JME.
  • Has a concurrent, confirmed diagnosis of non-epileptic seizures or events that can confound the assessment of the efficacy measures, in the opinion of the investigator.
  • The etiology of the participant's seizures is a progressive neurologic disease.
  • Has clinically unstable or progressive epilepsy.
  • Has clinically significant unstable medical condition(s), other than epilepsy, including unstable psychiatric disorders.
  • Has a history of status epilepticus in the 3 months prior to screening.
  • History of suicidal behavior, current suicidal risk as determined from history, or presence of active suicidal ideation as indicated by a positive response to Item 4 or Item 5 on the C-SSRS or is considered at risk of suicide or self-harm based on the clinical judgement of the investigator following interview with the participant and/or caregiver.
  • Has known or suspected hypersensitivity to cannabinoids or any of the excipients of the study intervention.
  • Is currently treated with Epidiolex or recently received treatment with Epidiolex within 28 days prior to screening.
  • Has a body weight < 20 kg or > 150 kg.
  • Is currently using or has used recreational or medicinal cannabis, cannabinoid/CBD based medications, products, or supplements (botanical or synthetic) within 28 days prior to screening.
  • Is unwilling or unable to abstain from recreational or medicinal cannabis, cannabinoid/CBD based medications, products, or supplements (botanical or synthetic) for the duration of the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Double blind
Primary purpose
Treatment

Study locations

United States · 10 centers
  • Clinical Trial Site — New Haven
  • Clinical Trial Site — Tampa
  • Clinical Trial Site — Atlanta
  • Clinical Trial Site — Savannah
  • Clinical Trial Site — Honolulu
  • Clinical Trial Site — Hawthorne
  • Clinical Trial Site — Cincinnati
  • Clinical Trial Site — Portland
  • … and 2 more centers

Identifiers

NCT: NCT07723963 · JZP926-203

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗