RecruitingPhase 2Phase 3NCT06999902

Double-blind, Randomized Trial of PRAX-628 in Adults With Focal Seizures to Evaluate Efficacy and Safety (POWER1)

A Double-Blind, Randomized, Multicenter, Trial Evaluating the Efficacy and Safety of PRAX-628 in Adults With Focal Seizures (POWER1)


Sponsor

Praxis Precision Medicines

Enrollment

230 participants

Start Date

Dec 11, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

A Double-Blind, Randomized, Multicenter, Trial Evaluating the Efficacy and Safety of PRAX-628 in Adults With Focal Seizures (POWER1)


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Inclusion Criteria2

  • A diagnosis of focal onset epilepsy according to the International League Against Epilepsy (ILAE) Classification of Epilepsy.
  • Past evidence by computed tomography (CT) or magnetic resonance imaging (MRI) that has ruled out a progressive cause of epilepsy in the judgement of the investigator and/or in consultation with the medical monitor.

Exclusion Criteria9

  • Subject has had any of the of the following within the 12-month period preceding trial entry: History of pseudo or psychogenic seizures, cluster seizures where the individual seizures cannot be counted, an episode of convulsive status epilepticus requiring hospitalization and intubation, or subject only has focal seizures with awareness that do not have motor activity.
  • Planned epilepsy surgery during the course of the clinical trial.
  • History of neurosurgery for seizures \<1 year prior to enrollment, or radiosurgery \<2 years prior to enrollment or vagus nerve stimulation (VNS) implantation.
  • History of schizophrenia, obsessive-compulsive disorder, or other serious mental health disorders.
  • History of malignancy, myeloproliferative or lymphoproliferative disorders within the past 5 years are excluded.
  • History of cardiac disease(s)/cardiac conduction disorders/or cardiac structural abnormality(ies).
  • Has a positive test result or a known history of a positive test result for human immunodeficiency virus (HIV), hepatitis B surface antigen (HBsAg), or anti-hepatitis C virus (HCV) antibody at Screening.
  • Is pregnant or is breastfeeding at the time of Screening or has a positive serum pregnancy test at Screening or is planning to become pregnant during the clinical trial or within 14 days of the last study drug dose.
  • Has received any other experimental or investigational drug, device or other therapy within 30 days or 5 half-lives (whichever is longer) prior to Screening, or any prior use of gene therapy.

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Interventions

DRUG20mg/day PRAX-628 for 6 weeks then 30mg/day PRAX-628 for remaining 6 weeks

Once daily oral

DRUGPlacebo

Once daily oral


Locations(26)

Praxis Research Site

Phoenix, Arizona, United States

Praxis Research Site

DeLand, Florida, United States

Praxis Research Site

Miami Lakes, Florida, United States

Praxis Research Site

Chicago, Illinois, United States

Praxis Research Site

Lafayette, Louisiana, United States

Praxis Research Site

Bethesda, Maryland, United States

Praxis Research Site

Chesterfield, Missouri, United States

Praxis Research Site

Ozark, Missouri, United States

Praxis Research Site

Hackensack, New Jersey, United States

Praxis Research Site

Middletown, New York, United States

Praxis Research Site

Canton, Ohio, United States

Praxis Research Site

Oklahoma City, Oklahoma, United States

Praxis Research Site

El Paso, Texas, United States

Praxis Research Site

Frisco, Texas, United States

Praxis Research Site

Round Rock, Texas, United States

Praxis Research Site

Seabrook, Texas, United States

Praxis Research Site

Barcelona, Spain

Praxis Research Site

Barcelona, Spain

Praxis Research Site

Barcelona, Spain

Praxis Research Site

Granda, Spain

Praxis Research Site

Madrid, Spain

Praxis Research Site

Madrid, Spain

Praxis Research Site

Madrid, Spain

Praxis Research Site

Málaga, Spain

Praxis Research Site

Terrassa, Spain

Praxis Research Site

Valencia, Spain

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NCT06999902


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