Safety, Tolerability, and Exploratory Efficacy of Adjunctive EQU-001 for Seizures in Adults With Epilepsy

NCT ID: NCT05063877

Last Updated: 2023-05-15

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 43 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-08-31
• Study Completion Date: 2023-10-11

Brief Summary

This is a double-blind, placebo controlled, randomized study of dose-ranging safety, tolerability, exploratory efficacy of adjunctive EQU-001 for seizures using the continuous reassessment method in patients diagnosed with epilepsy.

Detailed Description

EQU-201 is a Phase 2 randomized, double-blind, placebo-controlled study to evaluate dose-ranging safety, tolerability, and exploratory efficacy of adjunctive EQU-001 using the continuous reassessment method (CRM). 10 participants diagnosed with epilepsy according to the International League Against Epilepsy (ILAE) Classification of the Epilepsies 2017 criteria whose seizures are uncontrolled on one to four concomitant antiepileptic drugs (AEDs) for ≥4 weeks will be enrolled in 4 dose cohorts (10 mg, 20 mg, 40 mg, 60 mg) The participants will be randomized 4:1, drug to placebo. The dosing is for 12 weeks, after which, safety data will be reviewed post 14 days to determine whether the next cohort can be opened. Once the 12-week study dosing period is complete, all subjects may enroll in an open-label extension, during which period investigators may make dose adjustments down to 20 mg and up 80 mg.

This study of EQU-001 will provide safety of a range of doses, tolerability, and PK data in patients with epilepsy and aims to identify drug-specific DLTs and MTD. The PK component will characterize the PK of EQU-001 to inform dosing and may help to correlate exposures with any DLTs or other treatment-related AEs. The open label extension component will provide data on subject safety, tolerability and efficacy.

Conditions

Epilepsy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Placebo

Matched placebo control 10 mg capsule or 20 mg capsules totaling to 10 mg, 20 mg, 40mg or 60 mg will be administered once daily orally for 12 weeks with the option for open-label extension.

Intervention: Drug: Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Matched placebo

Study drug EQU-001

10mg capsules or 20 mg EQU-001 capsules totally 10 mg, 20 mg, 40 mg, 60 mg will be administered once orally daily to active-treatment subjects for 12-weeks with the option for open-label extension. During the open-label extension, subjects taking 60 mg dose for 4 weeks or longer may increase to 80 mg per day dose, at the discretion of the PI.

Intervention: Drug : EQU-001

Group Type: EXPERIMENTAL

EQU-001

Intervention Type: DRUG

EQU-001 in 10 mg and 20 mg capsules

Interventions

Placebo

Matched placebo

Intervention Type: DRUG

EQU-001

EQU-001 in 10 mg and 20 mg capsules

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Able to provide informed consent, or consent provided by a Legally Authorized Representative (LAR)

2. Diagnosed with epilepsy according to ILAE 2017 criteria and with uncontrolled countable seizures (as per Epilepsy Study Consortium review) on one to four concomitant anti-seizure medicines (AEDs) at optimal stable dosages for at least 4 weeks prior to screening and throughout the treatment period

3. Age 18 to 60 years of age

4. Must have had a brain MRI or CT scan with an available report (images need not be available) that is negative for other confounding conditions

5. Must have an EEG report consistent with the subject's seizure type(s)

6. Pre-menopausal females and males with pre-menopausal sexual partners should either be sexually inactive (abstinent) for 21 days prior to the first dose, throughout the study, and for 14 days following the last dose or, if heterosexually active, agree to use of one of the following acceptable birth control methods for the period above:

1. Intrauterine device (IUD) in place

2. Hormonal contraceptives plus barrier method

3. At least 2 barrier methods (condom, diaphragm) with spermicide

4. Surgical sterilization of participant or partner(s) (bilateral tubal ligation, hysterectomy, bilateral oophorectomy, vasectomy > 6 months ago)

7. Able and willing to adhere to protocol; the subject or selected observer can keep an accurate seizure diary

8. Before progressing from Baseline Period to Randomization:

1. A subject must experience at least 3 countable observable seizures per 4 weeks prior to randomization, including at least the 4-week baseline period.

2. These seizures may be generalized, focal, or of unknown onset, but may not include absence seizures or focal aware seizures without a detectable motor component, aphasia, or other observable symptom.

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Exclusion Criteria

1. Pregnant or lactating female

2. History of hypersensitivity to ivermectin

3. Ivermectin use within 28 days of screening

4. History of progressive neurological disorder or other significant progressive disorder or unstable medical condition(s)

5. Change in AED regimen in the 28 days prior to screening

6. Taking >4 concomitant AEDs at screening

7. History of status epilepticus in the 2 years prior to screening

8. A vagal nerve stimulator (VNS), responsive neurostimulator (RNS) or deep brain stimulator (DBS), implanted or activated <1 year prior to screening, or with stimulation parameters stable for <3 months or battery life of unit not anticipated to extend for the duration of the trial

9. History of traumatic brain injury within 28 days prior to screening

10. History of psychogenic non-epileptic seizures (PNES), active or within 2 years prior to study entry

11. Epilepsy-related surgery within 1 year prior to screening, epilepsy-related radiosurgery or laser surgery within 1 year prior to screening

12. Epilepsy dietary therapy initiated <3 months prior to screening

13. Psychiatric disorder in which changes in pharmacotherapy are needed or anticipated during the study

14. Active suicidal plan/intent in the 6 months prior to screening and evidenced by a positive response to C-SSRS questions 4 or 5, a history of suicide attempt in the 2 years prior to screening, or more than 1 lifetime suicide attempt.

15. Administration of investigational product in another trial within 28 days prior to the first expected study drug administration, or five half-lives, whichever is longer.

16. Receiving felbamate for <1 year prior to screening

17. Receiving vigabatrin for <2 years prior to screening. Subjects on vigabatrin should have available, appropriate documentation of visual fields

18. Receiving ezogabine (ex-US) at screening

19. Use of the following medications and foods at screening or baseline that may interfere with study drug:

1. CYP3A4 inducers: rifampin, lumacaftor, mitotane, enzalutamide, apalutamide, St. John's wort, glucocorticoids

2. CYP3A4 inhibitors including and not limited to: clarithromycin, ceritinib, idelalisib, lonafarnib, tucatinib, erythromycin, telithromycin, diltiazem, ketoconazole, posaconazole, voriconazole, telithromycin, nefazodone, mifepristone, itraconazole, ketoconazole, anti-retroviral drugs (atazanavir, darunavir, indinavir, lopinavir, nelfinavir, ritonavir, saquinavir, tipranavir), grapefruit and grapefruit juice, pomegranate and pomegranate juice

3. Additional medications that may interact with CYP3A4, PGP, or Vitamin K: fluconazole, isavuconazole, cyclosporine, amiodarone, dronaderone, verapamil, imatinib, warfarin, acenocoumarol

20. Has any of the following laboratory abnormalities at screening:

1. Positive COVID test

2. Positive urine drug screen (except as clinically indicated)

3. Total bilirubin or higher ≥1.5× the site laboratory upper limit of normal (ULN)

4. ALT or ALT ≥2× the site laboratory ULN

5. HbA1c >7.0%

6. Positive hCG (female participants) (screening or baseline)

21. Subject is not approved for study inclusion by the Epilepsy Consortium based on the diagnostic review form

22. Any condition that, in the opinion of the investigator, may impact a subject's safety or ability to follow study procedures.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Equilibre Biopharmaceuticals B.V.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ya-El Mandel-Portnoy, PhD

Role: STUDY_DIRECTOR

Equilibre

Locations

Consultants in Epilepsy and Neurology PLLC

Boise, Idaho, United States

Mid-Atlantic Epilepsy and Sleep Center

Bethesda, Maryland, United States

Northeast Regional Epilepsy Group

Hackensack, New Jersey, United States

NYU Langone Medical Center, NYU Comprehensive Epilepsy Center

New York, New York, United States

Comprehensive Epilepsy Center at Thomas Jefferson University

Philadelphia, Pennsylvania, United States

University of Virginia

Charlottesville, Virginia, United States

Hadassah Medical Center

Jerusalem, , Israel

Rabin Medical Center

Petah Tikva, , Israel

Chaim Sheba Medical center

Ramat Gan, , Israel

Tel Aviv Sourasky Medical Center

Tel Aviv, , Israel

Countries

United States; Israel

Other Identifiers

EQU-201

Identifier Type: -

Identifier Source: org_study_id