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Clinical trial information and results are updated daily from ClinicalTrials.gov. The latest data update was conducted on 06/15/2021.

A Study to Investigate the Long-Term Safety of ZX008 (Fenfluramine Hydrochloride) Oral Solution in Children and Adults With Epileptic Encephalopathy Including Dravet Syndrome and Lennox-Gastaut Syndrome

Clinicaltrials.gov identifier NCT03936777

Recruitment Status Enrolling by invitation

First Posted May 3, 2019

Last update posted September 17, 2020

Study Description

Brief summary:

This is an international, multicenter, open-label, long-term safety study of ZX008 in subjects with Dravet syndrome, Lennox-Gastaut syndrome or epileptic encephalopathy

  • Condition or Disease:Dravet Syndrome
    Lennox Gastaut Syndrome
    Epileptic Encephalopathy
  • Intervention/Treatment: Drug: ZX008 (Fenfluramine Hydrochloride)
  • Phase: Phase 3
Detailed Description

This is an international, multicenter, open-label, long-term safety study of ZX008 in patients with epileptic encephalopathy, including Dravet syndrome or Lennox-Gastaut syndrome. Subjects eligible for participation are those with Dravet syndrome who are currently enrolled in Study ZX008-1503, or those with Lennox-Gastaut syndrome who have successfully completed Study ZX008-1601-Part 2, and are candidates for continued treatment with ZX008 for an extended period of time, or those with Dravet syndrome, Lennox-Gastaut syndrome, or another epileptic encephalopathy who have completed participation in another Zogenix-sponsored study and have been invited to participate in this study.

Study Design
  • Study Type: Interventional
  • Estimated Enrollment: 650 participants
  • Intervention Model: Single Group Assignment
  • Intervention Model Description: Single Group Assisgnment
  • Masking: None (Open Label) ()
  • Primary Purpose: Treatment
  • Official Title: An Open-Label Extension Trial to Assess the Long-Term Safety of ZX008 (Fenfluramine Hydrochloride) Oral Solution as an Adjunctive Therapy for Seizures in Patients With Rare Seizure Disorders Such as Epileptic Encephalopathies Including Dravet Syndrome and Lennox-Gastaut Syndrome
  • Actual Study Start Date: April 2019
  • Estimated Primary Completion Date: April 2023
  • Estimated Study Completion Date: April 2023
Arms and interventions
Arm Intervention/treatment
Experimental: ZX008 (Fenfluramine Hydrochloride)
ZX008 is supplied as an open-label oral solution.Doses will include up to 0.8 mg/kg/day divided into 2 daily doses, up to a maximum of 30 mg/day (subjects taking concomitant STP will receive up to 0.5 mg/kg/day, up to a maximum of 20 mg/day) in a concentration of 2.5 mg/mL.
Drug: ZX008 (Fenfluramine Hydrochloride)
Fenfluramine hydrochloride provided in a concentration of 2.5 mg/mL.
Outcome Measures
  • Primary Outcome Measures: 1. Changes in respiratory rate [ Time Frame: Up to 36 months open-label ]
    The analysis will include change in resting respiratory rate using standard measure
  • 2. Change in Adverse Events and Serious Adverse Events leading to study withdrawal in subjects receiving open label ZX008 [ Time Frame: Up to 36 months open-label ]
    Evaluate the long term safety and tolerability of oral dose administration of ZX008
  • 3. Changes in laboratory test results [ Time Frame: Up to 36 months open-label ]
    The analysis will include abnormal hematology and chemistry laboratory results outside of reference ranges
  • 4. Changes in heart rate [ Time Frame: Up to 36 months open-label ]
    The analysis will include change in heart rate using standard measure
  • 5. Changes in blood pressure [ Time Frame: Up to 36 months open-label ]
    The analysis will include change in resting blood pressure using standard measure
  • 6. Change in body weight [ Time Frame: Up to 36 months open-label ]
    The analysis will include change in body weight and height by report of BMI in kg/m^2
  • 7. Changes in heart rhythm [ Time Frame: Up to 36 months open-label ]
    The analysis will include changes in heart beat as measured with 12-lead electrocardiogram
  • 8. Changes in heart valve function [ Time Frame: Up to 36 months open-label ]
    The analysis will include change in heart valves as measured with standard echocardiogram
  • Secondary Outcome Measures: 1. Change in convulsive seizure response [ Time Frame: Up to 36 months open-label ]
    The analysis will include percent improvement per investigator rating
  • 2. Change in Cognitive CGI by Parent/Caregiver [ Time Frame: Up to 36 months open-label ]
    The rating by parent/caregiver of the patient's change in cognitive symptoms since the beginning of study as "very much improved", "much improved", "minimally improved", "no change", "minimally worse", "much worse", or "very much worse".
  • 3. Change in Behavioral CGI by Parent/Caregiver [ Time Frame: Up to 36 months open-label ]
    The rating by parent/caregiver of the patient's change in behavioral symptoms since the beginning of study as "very much improved", "much improved", "minimally improved", "no change", "minimally worse", "much worse", or "very much worse".
  • 4. Change in Motor CGI by Parent/Caregiver [ Time Frame: Up to 36 months open-label ]
    The rating by parent/caregiver of the patient's change in motor symptoms since the beginning of study as "very much improved", "much improved", "minimally improved", "no change", "minimally worse", "much worse", or "very much worse".
  • 5. Change in Cognitive CGI by Investigator [ Time Frame: Up to 36 months open-label ]
    The rating by investigator of the patient's change in cognitive symptoms since the beginning of study as "very much improved", "much improved", "minimally improved", "no change", "minimally worse", "much worse", or "very much worse".
  • 6. Change in Behavioral CGI by Investigator [ Time Frame: Up to 36 months open-label ]
    The rating by investigator of the patient's change in behavioral symptoms since the beginning of study as "very much improved", "much improved", "minimally improved", "no change", "minimally worse", "much worse", or "very much worse".
  • 7. Change in Motor CGI by Investigator [ Time Frame: Up to 36 months open-label ]
    The rating by investigator of the patient's change in motor symptoms since the beginning of study as "very much improved", "much improved", "minimally improved", "no change", "minimally worse", "much worse", or "very much worse".
  • 8. Change in Clinical Global Impression by Parent/Caregiver [ Time Frame: Up to 36 months open-label ]
    The rating by parent/caregiver of the patient's overall change in symptoms since the beginning of study as "very much improved", "much improved", "minimally improved", "no change", "minimally worse", "much worse", or "very much worse"
  • 9. Change in Clinical Global Impression by Investigator [ Time Frame: Up to 36 months open-label ]
    The rating by investigator of the patient's overall change in symptoms since the beginning of study as "very much improved", "much improved", "minimally improved", "no change", "minimally worse", "much worse", or "very much worse"
Eligibility Criteria
  • Ages Eligible for Study: 2 Years and older (Child, Adult, Older Adult)
  • Sexes Eligible for Study: All
  • Accepts Healthy Volunteers: No
Criteria

Inclusion Criteria:

- Male or nonpregnant, nonlactating female

- Satisfactory completion of a core study

- Has a rare seizure disorder, such as epileptic encephalopathy and has successfully
completed another Zogenix-sponsored clinical trials with ZX008

- Subject's caregiver is willing and able to be compliant with study procedures, visit
schedule and study drug accountability

Exclusion Criteria:

- Current cardiac valvulopathy or pulmonary hypertension that is clinically significant

- Moderate or severe hepatic impairment

- Receiving monoamine oxidase inhibitors, serotonin agonists, serotonin antagonists, and
serotonin reuptake inhibitors within 14 days of receiving ZX008

Contacts and Locations
Contacts
Locations
Show 28 Study Locations
Sponsors and Collaborators

Zogenix, Inc.

Zogenix International Limited, Inc., a subsidiary of Zogenix, Inc.

More Information
  • Responsible Party: Zogenix, Inc.
  • ClinicalTrials.gov Identifier: NCT03936777 History of Changes
  • Other Study ID Numbers: ZX008-1900
  • First Posted: May 3, 2019 Key Record Dates
  • Last Update Posted: September 17, 2020
  • Last Verified: September 2020
  • Studies a U.S. FDA-regulated Drug Product: Yes
  • Studies a U.S. FDA-regulated Device Product: No
  • Additional relevant MeSH terms: Lennox Gastaut Syndrome
    Syndrome
    Epilepsy
    Epilepsies, Myoclonic
    Brain Diseases