Open Actively Recruiting

A Study of Lorcaserin as Adjunctive Treatment in Participants With Dravet Syndrome

About

Brief Summary

The primary purpose of the study is to demonstrate that lorcaserin has superior efficacy compared to placebo on percent change in frequency of convulsive seizures per 28 days in participants with Dravet syndrome.

Primary Purpose
Treatment
Study Type
Interventional
Phase
Phase III

Eligibility

Gender
All
Healthy Volunteers
No
Minimum Age
2 Years
Maximum Age
N/A

Key Inclusion Criteria:

Participants must meet all of the following criteria to be included in this study:

  • Male or female, age 2 years and older at the time of informed consent
  • Diagnosis of epilepsy with Dravet syndrome
  • Has at least 4 convulsive seizures during the 4 weeks of baseline
  • Current treatment with antiepileptic drugs must be stable for at least 4 weeks before screening, and be expected to remain stable throughout the study

Key Exclusion Criteria:

Participants who meet any of the following criteria will be excluded from this study:

  • Use of lorcaserin within 4 weeks before screening, or any history of it being discontinued due to lack of efficacy or adverse reactions
  • Use of fenfluramine within 2 months before screening, any history of lack of fenfluramine efficacy, or any history of valvulopathy at baseline with history of fenfluramine use
  • Recent or concomitant use of serotonergic medications or monoamine oxidase inhibitors
  • Presence of progressive central nervous system disease other than Dravet syndrome

Join this Trial

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Study Stats
Protocol No.
20-001662
Category
Neurology
Pediatrics
Urology
Contact
Angela Martinez
Location
  • UCLA Westwood
For Providers
NCT No.
NCT04572243
For detailed technical eligibility, visit ClinicalTrials.gov.