Menu
Recruiting NCT06769659

A Study Evaluating NPT 2042 Versus Placebo in Subjects Aged 16-75 Years With Genetic Generalized Epilepsy (GGE) and Absence Seizures

Phase II Interventional Epilepsy, Generalized Epilepsy, Absence

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: NPT 2042, Placebo.
Who it may be relevant to
Registry conditions: Epilepsy, Generalized, Epilepsy, Absence. Basic parameters: 16 years — 75 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 →

Unsure about the terms? Read our patient guide →

Official title

A Single-center, Double-blind, Placebo-controlled Crossover Study Evaluating NPT 2042 Versus Placebo in Subjects Aged 16-75 Years With Genetic Generalized Epilepsy (GGE) and Absence Seizures

Overview

This study will compare the effect of NPT 2042 and placebo in subjects with GGE on the frequency and duration of electroencephalographic absence seizures, separated by a 14-day washout period. The study will be a single-center, double-blind, crossover study with subjects receiving either NPT 2042 BID orally or matching placebo BID in each of two treatment periods. Two doses of NPT 2042 will be evaluated.

Interventions

  • Drug NPT 2042
    NPT 2042 is a new drug being developed as an anti-seizure treatment
  • Other Placebo
    Placebo Comparator

Primary outcome measures

  • Mean and median across subjects of the within subject difference in percent change from treatment period baseline of the frequency of absence seizures [Time frame: Up to 12 weeks]
Secondary outcome measures (6)
  • Mean and median across subjects of the within subject difference between NPT 2042 and placebo on absence seizures [Time frame: Up to 12 weeks]
  • Mean and median across subjects of the within subject categorical difference in percent change between NPT 2042 and placebo of the frequency of absence seizure [Time frame: Up to 12 weeks]
  • The proportion of NPT 2042- vs. placebo-treated subjects meeting the study specific response criteria [Time frame: Up to 12 weeks]
  • The mean change from Baseline across subjects of the within subject difference between NPT 2042 and placebo on the Quality of Life in Epilepsy Questionnaire (QOLIE-31-P) [Time frame: Up to 12 weeks]
  • The mean change from Baseline in the Digit Symbol Substitution Test [Time frame: Up to 12 weeks]
  • The mean change from Baseline in the Epworth Sleepiness Scale [Time frame: Up to 12 weeks]

Eligibility criteria

Inclusion criteria

  • Subject is capable of and provides consent/assent, and the study participant's parent/legal representative/caregiver provides signed informed consent for minor study participants, which includes compliance with the requirements and restrictions listed in the informed consent form (ICF)
  • Subject is aged 16-75 years at the time of consent/assent
  • Subject is diagnosed with genetic generalized epilepsy with absence seizures (consistent with the International League Against Epilepsy (ILAE) Classification of Seizures (2017))
  • Subject has electroencephalogram (EEG) evidence of bilateral synchronous generalized paroxysmal spike-wave (2.5 Hz to 6 Hz) bursts lasting 3 seconds or more at least 4 times on the screening 72-hour ambulatory EEG.
  • Subject has been on a stable dose of at least one antiseizure medication (ASM) for at least 30 days. Vagal nerve stimulation at stable settings (for at least 30 days before screening), without use of the magnet, is also acceptable.
  • Subject has normal cognition and no clinically significant abnormalities on neurological examination at screening in the opinion of the Investigator
  • Subject is in otherwise good health (with the exception of epilepsy), as determined by the investigator, and as documented in the medical history, physical examination, and screening laboratory investigations
  • Subject has a body mass index (BMI) between 18 and 40 kg/m2 inclusive, at screening
  • Female subjects of child-bearing potential and all men agree to use of highly effective methods of contraception during the study and for 28 days after last dose of study drug
  • Subject (and parent/caregiver, if applicable) is able to communicate with the investigator and to understand and comply with all study requirements, including the clinic visit schedule

Exclusion criteria

  • Subject has metabolic or mitochondrial encephalopathies, seizures associated with structural abnormalities, or infection-related seizures.
  • Subject has a developmental epileptic encephalopathy (e.g. Lennox-Gastaut syndrome)
  • Subject has a history of convulsive status epilepticus within the past year.
  • Subject has a history of surgical intervention for treatment of epilepsy
  • Subject has a history of nonepileptic seizures (e.g., metabolic, structural, or paroxysmal non epileptic seizures)
  • Subject has severe intellectual disability, severe autism spectrum disorder, or severe developmental disorder such that the subject cannot consent or assent to participate or cannot cooperate with the study procedures
  • Female subject who is pregnant or lactating
  • Subject has any clinically significant laboratory abnormality which, in the opinion of the investigator, will exclude the subject from the study
  • Subject has an active CNS infection, demyelinating disease, degenerative neurological disease, or any CNS disease deemed to be progressive during the course of the study that may confound the interpretation of the study results
  • Subject has any clinically significant psychiatric illness, psychological or behavioral problems which, in the opinion of the investigator, would interfere with the subject's ability to participate in the study, including but not limited to the following:
  • Subject has active suicidal ideation prior to study entry as indicated by a positive response ("yes") to either Question 4 or Question 5 of the Columbia Suicide Severity Rating Scale (C-SSRS)
  • Study participant has a lifetime history of suicide attempt (including an active attempt, interrupted attempt, or aborted attempt)
  • Subject is suffering from clinically significant active liver disease, porphyria or has a family history of severe hepatic dysfunction indicated by abnormal liver function tests greater than three times the upper limit of normal (AST and ALT)
  • Subject has a DSM-V diagnosis of alcohol or drug abuse, or drug addiction within the past 12 months
  • Subject has participated in any other trials involving an investigational product or device within 30 days of screening or longer, as required by local regulations
  • Subject is currently using prohibited medications or products
  • Subject is unable to complete ingestion of four placebo SGCs with a minimum of eight ounces of water at screening
  • Subject (and parent/caregiver, if applicable) has daily commitments during the study duration that would interfere with attending all study visits
  • Positive urine drug test for substance of abuse or illegal recreational substances at screening

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
Crossover
Masking
Quadruple blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • Clinical Trials, Inc. (CTI) — Little Rock

Identifiers

NCT: NCT06769659 · NPT 2042 CL-200

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗