Efficacy, Safety and Pharmacokinetics of ES-481 in Adult Patients With Drug Resistant Epilepsy

Phase 2

Recruiting

• Conditions: Drug Resistant Epilepsy
• Interventions: Drug: Open-Label Extension Study; Drug: ES-481; Drug: Placebo

• Registration Number: NCT04714996
• Lead Sponsor: ES Therapeutics Australia Pty Ltd

Brief Summary

This is a Phase 2a, Randomized, Double-Blind, Placebo-Controlled Study with cross-over to Evaluate the Efficacy, Safety, and Pharmacokinetics of ES-481 in Adult Patients with Drug Resistant Epilepsy

Detailed Description

Not available

Study Timeline

• Study Start: 2020-10-30
• Study First Submitted: 2021-01-13
• Study First Submitted QC: 2021-01-14
• Study First Posted: 2021-01-20
• Status Verified: 2023-03
• Last Update Submitted: 2023-03-01
• Last Update Posted: 2023-03-02
• Primary Completion: 2023-12
• Study Completion: 2023-12

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 24

Inclusion Criteria

1. The subject/legal guardian must be able to understand and sign the Human Research Ethics Committee-approved written Informed Consent Form (ICF) and privacy language as per national regulations (e.g., HREC and TGA requirement in Australia) prior to any study-related procedures being performed

2. The subject is a male or female 18 to 70 years of age, inclusive

3. The subject must have a history of drug resistant epilepsy (as per the ILAE definition)

4. The subject must be taking 1 to 4 antiepileptic drugs (AED) and must be on a stable dose of the AEDs for at least four (4) weeks prior to entering the 28-day screening period

5. If VNS implanted, the stimulation setting must have been stable for at least four weeks prior to entering the 28-day screening period

6. The subject/legal guardian must be able to use the seizure dairy to record seizure throughout the study

7. The subject must experience at least four (4) countable seizures within a 28-day period.

   For continued enrollment into Treatment Period 1, each subject will be confirmed to have experienced at least four (4) countable seizures in the 28-day screening period

8. The subject must have interictal epileptiform discharges and/or seizure with an average frequency of at least one (1) per hour on EEG recording.

   For continued enrollment into Treatment Period 1, this will be confirmed by a 24-hour EEG performed during the 28-day screening period.

9. The subject is willing and able to comply with the study requirements

Exclusion Criteria

1. Unwilling or inability to follow the procedures specified by the protocol

2. Pregnancy or breast feeding

3. Women of child-bearing potential and men who are unable or unwilling to take adequate contraceptive precautions, including one of the following:

   Hormonal contraception (birth control pills, injected hormones or vaginal ring) Intrauterine device Barrier methods (condom or diaphragm) combined with spermicideSurgical sterilization (hysterectomy, tubal ligation, or vasectomy)

4. Current treatment for another significant medical disorder, such as diabetes, or heart disease or an untreated disorder, that is discovered during the 28-day screening period and might interfere with the study in the opinion of the Principal Investigator

5. An abnormality on clinical laboratory tests, physical examination, EEG or ECG that might increase the risks associated with trial participation or investigational product administration, such as hepatic enzyme elevation greater than twice normal and/or a GFR < 60 mL/min/1.73 m2

6. History (within the month) of illicit drug use or alcohol dependence, and a commitment by the subject to not take the illicit drugs during the study

7. Concomitant treatment with more than four (4) AEDs

8. Evidence for a potentially progressive neurologic disorder, such as a brain tumor, multiple sclerosis or dementia

9. Planned epilepsy surgery within six months of enrollment

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: CROSSOVER

Arm && Interventions

Group	Intervention	Description
Open-Label Extension Study	Open-Label Extension Study	-
ES-481	ES-481	-
Placebo	Placebo	-

Primary Outcome Measures

Name	Time	Method
Seizure Frequency	Continuous and at Days 1, 8, 15, 22, 28, 43, 50, 57, 64 and 70	A change in seizure frequency and activity assessed using a patient diary and continuous 24-hour EEG monitoring (composite outcome)

Secondary Outcome Measures

Name	Time	Method
Hamilton Anxiety Rating Scale (HAM-A)	Collected at screening, Days 1, 8, 15, 22, 28, 43, 50, 57, 64 and 70	To assess for changes in the HAM-A
Hamilton Depression Rating Scale (HDRS)	Collected at screening, Days 1, 8, 15, 22, 28, 43, 50, 57, 64 and 70	To assess for changes in HDRS
Pharmacokinetics (PK) - AUC0-t	Collected at screening, Days 1, 8, 15 22, 28, 43, 50, 57, 64 and 70	Plasma concentration-time data will be analyzed using non compartmental methods to determine the following PK parameter: AUC0-t
Laboratory Assessments - Hematology	Collected at screening, Days 1, 8, 15 22, 28, 43, 50, 57, 64 and 70	Assess changes in hematology and chemistry laboratories by blood and serum assays and analysis
Adverse Events	Collected at screening, Days 1, 8, 15 22, 28, 43, 50, 57, 64 and 70	Monitoring clinically for adverse events for both CNS and Cardiovascular events
Laboratory Assessments - Chemistry	Collected at screening, Days 1, 8, 15 22, 28, 43, 50, 57, 64 and 70	Assess changes in hematology and chemistry laboratories by blood and serum assays and analysis
Pharmacokinetics (PK) - Cmax	Collected at screening, Days 1, 8, 15 22, 28, 43, 50, 57, 64 and 70	Plasma concentration-time data will be analyzed using non compartmental methods to determine the following PK parameter: Cmax
Pharmacokinetics (PK) - Tmax	Collected at screening, Days 1, 8, 15 22, 28, 43, 50, 57, 64 and 70	Plasma concentration-time data will be analyzed using non compartmental methods to determine the following PK parameter: Tmax
Pharmacokinetics (PK) - CL/F	Collected at screening, Days 1, 8, 15 22, 28, 43, 50, 57, 64 and 70	Plasma concentration-time data will be analyzed using non compartmental methods to determine the following PK parameter: CL/F
Pharmacokinetics (PK) - AUC0-inf. T1/2	Collected at screening, Days 1, 8, 15 22, 28, 43, 50, 57, 64 and 70	Plasma concentration-time data will be analyzed using non compartmental methods to determine the following PK parameter: AUC0-inf. T1/2
Pharmacokinetics (PK) - Vz/F	Collected at screening, Days 1, 8, 15 22, 28, 43, 50, 57, 64 and 70	Plasma concentration-time data will be analyzed using non compartmental methods to determine the following PK parameter: Vz/F

Trial Locations

Locations (4)

Royal Melbourne Hospital; 🇦🇺 Parkville, Victoria, Australia

Alfred Health; 🇦🇺 Melbourne, Victoria, Australia

Royal Brisbane and Women's Hospital; 🇦🇺 Herston, Queensland, Australia

Austin Hospital; 🇦🇺 Heidelberg, Victoria, Australia