A Two-Part Study of ZX008 in Children and Adults with Lennox-Gastaut Syndrome (LGS); Part 1: A Randomized, Double-blind, Placebo-controlled Trial of Two Fixed Doses of ZX008 (Fenfluramine Hydrochloride) Oral Solution as Adjunctive Therapy for Seizures in Children and Adults with LGS, Followed by Part 2: An Open-label Extension to Assess Long-Term Safety of ZX008 in Children and Adults with LGS

• Register: EUCTR
• Last refreshed on: 12 April 2021
• Main ID: EUCTR2017-002628-26-DE
• Date of registration: 11/04/2018
• Prospective Registration: Yes
• Primary sponsor: Zogenix International Limited, a wholly owned subsidiary of Zogenix Inc.
• Public title: A Two-Part Study of ZX008 in Children and Adults with Lennox-Gastaut Syndrome (LGS); Part 1: A Randomized, Double-blind, Placebo-controlled Trial of Two Fixed Doses of ZX008 (Fenfluramine Hydrochloride) Oral Solution as Adjunctive Therapy for Seizures in Children and Adults with LGS, Followed by Part 2: An Open-label Extension to Assess Long-Term Safety of ZX008 in Children and Adults with LGS
• Scientific title: A Two-Part Study of ZX008 in Children and Adults with Lennox-Gastaut Syndrome (LGS); Part 1: A Randomized, Double-blind, Placebo-controlled Trial of Two Fixed Doses of ZX008 (Fenfluramine Hydrochloride) Oral Solution as Adjunctive Therapy for Seizures in Children and Adults with LGS, Followed by Part 2: An Open-label Extension to Assess Long-Term Safety of ZX008 in Children and Adults with LGS
• Date of first enrolment: 15/11/2018
• Target sample size: 250
• Recruitment status: Authorised-recruitment may be ongoing or finished
• URL: https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2017-002628-26
• Study type: Interventional clinical trial of medicinal product
• Study design: Controlled: yes; Randomised: yes; Open: no; Single blind: no; Double blind: yes; Parallel group: yes; Cross over: no; Other: no; If controlled, specify comparator, Other Medicinial Product: no; Placebo: yes; Other: no; Number of treatment arms in the trial: 3
• Phase: Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no

Countries of recruitment

Australia, Austria, Belgium, Canada, Denmark, Finland, France, Germany, Ireland, Israel, Italy, Japan, Mexico, Netherlands, Poland, Spain, Sweden, Switzerland, United Kingdom, United States

Contacts

• Name: John Elie, Associate PD
• Affiliation: Syneos Health

• Name: John Elie, Associate PD
• Affiliation: Syneos Health

Key inclusion & exclusion criteria

Inclusion criteria:
1. Subject is male or nonpregnant, nonlactating female, age 2 to 35 years, inclusive as of the day of the Screening Visit. Female subjects of
childbearing potential must not be pregnant or breast-feeding. Female subjects of childbearing potential must have a negative urine or serum pregnancy test at screening. Subjects of childbearing or childfathering potential must be willing to use medically acceptable forms of birth control, which includes abstinence, while being treated on this study and for 90 days after the last dose of study drug
2. Subject must have a diagnosis of LGS, where seizures that result in drops are not completely controlled by current antiepileptic treatments. (Subjects without a formal diagnosis may still be enrolled at Sponsor discretion if all other criteria are met)
3.Subjects must meet all of the following 4 criteria for GLS, as defined in this protocol:
a.Onset of seizures at 11 years of age or younger
b.Multiple seizure types (must include TS or TA), including countable motor seizures that result in drops. Countable motor seizure types
eligible for inclusion are: GTC, TS, CS, AS, FS with observable motor symptoms, and MS that result in a drop
c.Abnormal cognitive development
d.Evidence of EEG in the medical history that shows abnormal background activity accompanied by slow spike and wave pattern <2.5
Hz(Acceptable evidence includes a copy of the EEG trace, EEG report, or physician note that appropriately describes the EEG findings.)
4.Subject must have had at least 8 drop seizures in the last 4 weeks prior to Screening (minimum of 4 drop seizures in the first two weeks
and 4 in the last two weeks before baseline), by parent/guardian report to Investigator or investigator medical notes
5.Receiving at least 1 concomitant AED and up to 4 concomitant AEDs, inclusive. The KD and VNS are permitted but do not count towards the total number of AEDs. Rescue medications for seizures are not counted towards the total number of AEDs
6.All medications or interventions for epilepsy (including KD and VNS) must be stable for at least 4 weeks prior to screening and are expected to remain stable throughout the study
7.Subject has been informed of the nature of the study and informed consent has been obtained from the legally responsible parent/guardian.
8.Subject has provided assent in accordance with Institutional Review Board (IRB)/Ethics Committee requirements, if capable
9.Subject's parent/caregiver is willing and able to be compliant with diary completion, visit schedule and study drug accountability
Randomization:
1.Subject has been approved for study inclusion by the Epilepsy Study Consortium
2.Subject does not have an exclusionary cardiovascular or cardiopulmonary abnormality based on ECHO, ECG or physical examination and is approved for entry by the central cardiac reader. Exclusionary abnormalities include, but are not limited to:
a.Trace or greater mitral or aortic valve regurgitation in subjects <18 years of age
b.Mild or greater mitral or aortic valve regurgitation in subjects >18 years of age
c.Possible signs of pulmonary hypertension with abnormal or greater than upper range of normal values
d.Evidence of left ventricular dysfunction (systolic or diastolic)
3.Subject demonstrates a stable baseline with = 2 seizures per week resulting in drops during the 4-week Baseline Period
4.Subject's parent/caregiver has been compliant with diary completion during the Baseline Period, in the opinion
Exclusion criteria:
1. Subject has a known hypersensitivity to fenfluramine or any of the excipients in the study medication.
2. Subject’s etiology of seizures is a degenerative neurological disease.
3. Subject has a history of hemiclonic seizures in the first year of life.
4. Subject only has drop seizures in clusters, where individual seizures cannot be counted reliably.
5. Subject has pulmonary arterial hypertension.
6. Subject has current or past history of cardiovascular or cerebrovascular disease, such as cardiac valvulopathy, myocardial infarction or stroke, or clinically significant structural cardiac abnormality, including but not limited to mitral valve prolapse, atrial or ventricular septal defects, patent ductus arteriosis (note: Patent Foramen Ovale or a bicuspid valve are not considered exclusionary).
7. Subject has current or recent history of Anorexia Nervosa, bulimia, or depression within the prior year that required medical treatment or psychological treatment for a duration greater than 1 month.
8. Subject has a current or past history of glaucoma.
9. Subject has had an anoxic episode requiring resuscitation within 6 months of the Screening Visit.
10. Subject has moderate or severe hepatic impairment. Asymptomatic subjects with mild hepatic impairment (elevated liver enzymes < 3x ULN and/or elevated bilirubin <2x ULN) may be entered into the study after review and approval by the Medical Monitor in conjunction with the sponsor, in consideration of comorbidities and concomitant medications.
11. Subject has severe renal impairment (estimated glomerlular filtration rate <30mL/min/1.73m2)
12. Subject is receiving concomitant therapy with any of the following: centrally-acting anorectic agents; monoamine-oxidase inhibitors; any centrally-acting compound with clinically appreciable amount of serotonin agonist or antagonist properties, including serotonin reuptake inhibition; other centrally-acting noradrenergic agonists, including atomexetine; or cyproheptadine (see Appendix 1 for a complete list of prohibited medications). (Note: Short-term medication requirements for prohibted medications will be handled on a per case basis by the Medical Monitor.)
13. Subject has positive result on urine tetrahydrocannabinol (THC) Panel or whole blood cannabidiol (CBD) at the Screening Visit.
14. Subject is taking felbamate for less than 1 year prior to screening and/or does not have stable liver function and hematology laboratory tests, and/or the dose has not been stable for at least 60 days prior to the Screening Visit.
15. Subject is known to be human immunodeficiency virus (HIV) positive.
16. Subject is known to have active viral hepatitis (B or C)
17. Subject is currently receiving an investigational product.
18. Subject has participated in another clinical trial within the past 30 days (calculated from that study’s last scheduled visit). Participation in non-treatment trials will be reviewed by the medical monitor.
19. Subject is at imminent risk of self-harm or harm to others, in the investigator’s opinion, based on clinical interview and responses provided on the Columbia-Suicide Severity Rating Scale (C-SSRS). Subjects must be excluded if they report suicidal behavior in the past 6 months as measured by the C-SSRS at Screening or Baseline, which includes suicidal ideation with intent and plan (Item #5). If a subject reports suicidal ideation on Item 4 without specific plan, and the investigator feels that the subject is appr

Age minimum:
Age maximum:
Gender:
Female: yes
Male: yes

Health Condition(s) or Problem(s) studied

Lennox-Gastaut Syndrome in Children and Adults
MedDRA version: 20.1 Level: PT Classification code 10048816 Term: Lennox-Gastaut syndrome System Organ Class: 10029205 - Nervous system disorders

Therapeutic area: Diseases [C] - Nervous System Diseases [C10]

Intervention(s)

Product Name: FENFLURAMINE HYDROCHLORIDE
Pharmaceutical Form: Oral solution
INN or Proposed INN: Fenfluramine
CAS Number: 404-82-0
Current Sponsor code: ZX008
Other descriptive name: Fenfluramine HCl, DL-Fenfluramine, (±)-Fenfluramine
Concentration unit: mg/ml milligram(s)/millilitre
Concentration type: equal
Concentration number: 5-
Pharmaceutical form of the placebo: Oral solution
Route of administration of the placebo: Oral use

Product Name: FENFLURAMINE HYDROCHLORIDE
Pharmaceutical Form: Oral solution
INN or Proposed INN: Fenfluramine
CAS Number: 404-82-0
Current Sponsor code: ZX008
Other descriptive name: Fenfluramine HCl, DL-Fenfluramine, (±)-Fenfluramine
Concentration unit: mg/ml milligram(s)/millilitre
Concentration type: equal
Concentration number: 2.5-
Pharmaceutical form of the placebo: Oral solution
Route of administration of the placebo: Oral use

Product Name: FENFLURAMINE HYDROCHLORIDE
Pharmaceutical Form: Oral solution
INN or Proposed INN: Fenfluramine
CAS Number: 404-82-0
Current Sponsor code: ZX008
Other descriptive name: Fenfluramine HCl, DL-Fenfluramine, (±)-Fenfluramine
Concentration unit: mg/ml milligram(s)/millilitre
Concentration type: equal
Concentration number: 1.25-
Pharmaceutical form of the placebo: Oral solution
Route of administration of the placebo: Oral use

Primary Outcome(s)

Secondary Objective: The key secondary objectives of Part 1 are:
• To evaluate the effect of ZX008 0.2 mg/kg/day versus placebo as adjunctive therapy for the treatment of uncontrolled seizures in children and adults with LGS based on the change in frequency of seizures that result in drops between baseline and T+M.
• To evaluate the effect of ZX008 0.2 and 0.8 mg/kg/day (independently) versus placebo on the proportion of subjects who achieve a =50% reduction from baseline in the frequency of seizures that result in drops.
• To evaluate the effect of ZX008 0.2 and 0.8 mg/kg/day (independently) versus placebo on the Clinical Global Impression –
Improvement rating, as assessed by the Principal Investigator.
In order to review the secondary objectives of Part 2 please refer to the section 2.2.2. of the protocol amendment 2.1 dated 29 July 2019

Timepoint(s) of evaluation of this end point: Data from Part 1 will constitute the primary analyses of the study and will be performed upon database lock after the last subject enrolled has completed the last study visit of Part 1.
The frequency of seizures that result in drops during the Part 2 OLE Treatment Period will be compared to baseline frequency measured prior to randomization in Part 1. Both the mean and median change from baseline will be presented and the statistical significance of the change will be assessed using a Wilcoxon signed-rank test. Other secondary assessments will be compared to baseline from prior to Part 1, or by visit throughout Part 1 and Part 2, as appropriate.

Main Objective: The primary objective of Part 1 is the primary objective of the entire study.
The primary objective of Part 1 is:
• To evaluate the effect of ZX008 0.8 mg/kg/day versus placebo as adjunctive therapy for the treatment of uncontrolled seizures in children and adults with Lennox-Gastaut syndrome (LGS) based on the change in frequency of seizures that result in drops between baseline and the combined Titration and Maintenance Periods (T+M).
The primary objective of Part 2 is to assess the long-term safety and tolerability of ZX008 in children and adults with LGS with regard to
adverse events (AEs), laboratory parameters, physical examination, neurological examination, cognition (BRIEF), vital signs (blood pressure,
heart rate, temperature, and respiratory rate), ECG, ECHO, body weight, and BMI.

Primary end point(s): Efficacy endpoints Part 1:
• Percent change from baseline in the frequency of seizures that result in drops in the combined Titration and Maintenance Periods (T+M) in the ZX008 0.8 mg/kg/day group compared to the placebo group.
Efficacy endpoints Part 2:
• The change from baseline in the frequency of seizures that result in drops.
• The change from baseline in the frequency of all countable motor seizures (GTC, TS, CS, AS, TA, FS, MS with a drop)
• The change from baseline in the frequency of all countable seizures
• The proportion of subjects who achieve a worsening from baseline (ie, <= 0% reduction), or >0%, = 25%, = 50%, = 75%, 100% reduction, and "near seizure freedom" (ie, 0 or 1 seizures) from baseline in frequency of all countable seizures that result in drops, countable motor seizures that do not result in drops, all countable motor seizures, all countable seizures, and all countable seizures that do not result in drops
• Number of seizure-free days, defined as 1) days with no countable seizures and 2) days with no seizures that result in drops
• Longest interval between seizures that result in drops
• Clinical Global Impression – Improvement rating, as assessed by the Principal Investigator.
• Clinical Global Impression – Improvement rating, as assessed by the parent/caregiver.

Secondary Outcome(s)

Secondary end point(s): • Change from baseline in the frequency of seizures that result in drops in T+M in the ZX008 0.2 mg/kg/day group compared to the placebo group.
• Proportion of subjects who achieve a =50% reduction from baseline in the frequency of seizures that result in drops comparing the ZX008 0.8 mg/kg/day and 0.2 mg/kg/day groups independently versus placebo
• Proportion of subjects who achieve clinically-meaningful improvement (much or very much improved) in the Clinical Global Impression –
Improvement as assessed by Principal Investigator comparing the ZX008 0.8 mg/kg/day and 0.2 mg/kg/day groups independently versus placebo.
Additional Secondary Endpoints:
ZX008 0.8 mg/kg/day and 0.2 mg/kg/day groups compared independently versus placebo on the
• Change from baseline in the frequency of all countable motor seizures in T+M
o Countable seizures include: generalized tonic-clonic seizures [GTC], tonic seizures [TS], clonic seizures [CS], atonic seizures [AS], tonic/atonic seizures [TA], clearly recognizable focal seizures [FS], and myoclonic seizures [MS] that result in a drop
• Change from baseline in the frequency of countable seizures that result in drops
• Change from baseline in the frequency of seizures that result in drops between baseline and the Maintenance Period (M)
• Change from baseline in the frequency of countable seizures that do not result in drops
• Proportion of subjects who achieve a worsening from baseline (ie, = 0% reduction), or >0% , =25%, =50%, =75%, 100% reduction, and
"near seizure freedom" (ie, 0 or 1 seizures) between baseline and T+M, and baseline and M, in all countable motor seizures; in countable motor seizures that do not result in drops; in all countable seizures; in all countable seizures that do not result in drops; and in all seizures that result in drops
• Number of seizure-free days in the baseline, M, and T+M period, defined as 1) days with no countable seizures and 2) days with no seizures that result in drops
• The longest interval (days) between seizures that result in drops comparing the ZX008 0.8 mg/kg/day and 0.2 mg/kg/day groups independently versus placebo
• Clinical Global Impression – Improvement as assessed by parent/caregiver The efficacy endpoints for Part 2 of the study are:
• The change from baseline in the frequency of seizures that result in drops.

Timepoint(s) of evaluation of this end point: NA

Secondary ID(s)

132604

2017-002628-26-BE

ZX008-1601

Source(s) of Monetary Support

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

Ethics review

Status: Approved
Approval date: 18/05/2018
Contact: