Safety, Tolerability, and Exploratory Efficacy of Adjunctive EQU-001 for Seizures in Adults With Epilepsy
Study Details
Study Description
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 2 |
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 10 mg and up to the dose at which a cohort has not met stopping criteria and has completed at least 14 days of dosing.
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.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Placebo Comparator: 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 |
Drug: Placebo
Matched placebo
|
| Experimental: 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. Intervention: Drug : EQU-001 |
Drug: EQU-001
EQU-001 in 10 mg and 20 mg capsules
|
Outcome Measures
Primary Outcome Measures
- Comparison of Grade 2 or higher, as defined by National Cancer Institute Common Terminology Criteria for Adverse Events, Version 5.0, November 2017, treatment-related adverse events (TRAEs) in each dose cohort as compared with placebo. [Upto 84 days]
Secondary Outcome Measures
- Change in the Quality of Life in Epilepsy-31-P (QOLIE-31-P) scale score as compared with baseline in treatment cohort as compared with placebo. [Day 84]
Maximum score: 100, Minimum score: 0, Higher scores reflect better quality of life, lower scores reflect lower quality of life.
- Change in C-SSRS responses as compared with baseline in treatment cohort as compared with placebo. [Day 84]
- Median change in the number of countable seizures overall and by seizure type (focal, generalized, and unknown onset). [Day 14, 42, 70, 98]
- Median change in the number of generalized tonic-clonic and focal to generalized tonic-clonic seizures. [Day 14, 42, 70, 98]
- Percent (%) of subjects who are seizure free. [Day 1 upto day 84]
- Number of subjects who withdraw from treatment because of study-drug effects. [Upto 14 days]
- Number of subjects in each dose cohort who decrease their dose of study drug because of treatment-related effects. [Upto 14 days]
- Correlation of plasma levels of EQU-001 with % seizure reduction [Weeks 2, 4, 8, 12]
- Correlation of plasma levels of biomarkers with % seizure reduction [Weeks 4, 8, 12]
- Seizure freedom in treated subjects overall and at each dose as compared with placebo. [Weeks 3 to 12 and Weeks 1 to 12 relative to the baseline observation period]
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Able to provide informed consent, or consent provided by a Legally Authorized Representative (LAR)
-
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
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Age 18 to 70 years of age
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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
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Must have an EEG report consistent with the subject's seizure type(s)
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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:
-
Intrauterine device (IUD) in place
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Hormonal contraceptives plus barrier method
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At least 2 barrier methods (condom, diaphragm) with spermicide
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Surgical sterilization of participant or partner(s) (bilateral tubal ligation, hysterectomy, bilateral oophorectomy, vasectomy > 6 months ago)
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Able and willing to adhere to protocol; the subject or selected observer can keep an accurate seizure diary
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Before progressing from Baseline Period to Randomization:
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A subject must experience at least 3 countable seizures per 4 weeks prior to randomization, including at least the 4-week baseline period.
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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.
Exclusion Criteria:
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Pregnant or lactating female
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History of hypersensitivity to ivermectin
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Current ivermectin use
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History of progressive neurological disorder or other significant progressive disorder or unstable medical condition(s)
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Change in AED regimen in the 28 days prior to screening
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Taking >4 concomitant AEDs at screening
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History of status epilepticus in the 2 years prior to screening
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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
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History of traumatic brain injury within 28 days prior to screening
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History of psychogenic non-epileptic seizures (PNES), active or within 2 years prior to study entry
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Epilepsy-related surgery within 1 year prior to screening, epilepsy-related radiosurgery or laser surgery within 1 year prior to screening
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Epilepsy dietary therapy initiated <3 months prior to screening
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Psychiatric disorder in which changes in pharmacotherapy are needed or anticipated during the study
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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.
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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.
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Receiving felbamate for <1 year prior to screening
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Receiving vigabatrin for <2 years prior to screening. Subjects on vigabatrin should have available, appropriate documentation of visual fields
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Receiving ezogabine (ex-US) at screening
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Use of the following medications and foods at screening or baseline that may interfere with study drug:
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CYP3A4 inducers: rifampin, lumacaftor, mitotane, enzalutamide, apalutamide, St. John's wort, glucocorticoids
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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
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Has any of the following laboratory abnormalities at screening or baseline:
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Positive COVID test
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Positive urine drug screen
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Total bilirubin or higher ≥1.5× the site laboratory upper limit of normal (ULN)
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ALT or ALT ≥2× the site laboratory ULN
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HbA1c >6.5%
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Positive hCG (female participants)
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Subject is not approved for study inclusion by the Epilepsy Consortium based on the diagnostic review form
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Any condition that, in the opinion of the investigator, may impact a subject's ability to follow study procedures.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Consultants in Epilepsy and Neurology PLLC | Boise | Idaho | United States | 83702 |
| 2 | Mid-Atlantic Epilepsy and Sleep Center | Bethesda | Maryland | United States | 20817 |
Sponsors and Collaborators
- Equilibre Biopharmaceuticals B.V.
Investigators
- Study Director: Amy Melsaether, MD, Equilibre
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- EQU-201