The ENACT trial is designed to evaluate the efficacy and safety of ENX-101 administered adjunctively to current therapy in reducing seizure frequency in patients diagnosed with focal (partial onset) epilepsy and treated with 1 to 4 antiseizure medications yet still experiencing seizures.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Adjunctive treatment to current antiseizure medication
To evaluate the efficacy of ENX-101 administered adjunctively with 1 to 4 antiseizure medications for the treatment of focal seizures
The median percent change from baseline in 28-day focal seizure frequency (focal aware motor with observable component, focal impaired awareness, or focal to bilateral tonic-clonic seizures) compared to placebo
Time frame: Day 1 to end of the Treatment Period (Day 56) compared to placebo
To evaluate the efficacy of ENX-101 administered adjunctively with 1 to 4 antiseizure medications for the treatment of focal seizures
The responder rate defined as the percent of patients who experience a 50% or greater reduction from baseline in seizure frequency in the Treatment Period compared to placebo (designated as primary for the European Medicines Agency)
Time frame: Treatment Period (Day 1 to Day 56) compared to placebo
To evaluate the efficacy of ENX-101
The percent of patients who are seizure free during the last 28 days of the Treatment Period
Time frame: Treatment Period (Day 29 to Day 56) compared to placebo
To evaluate the efficacy of ENX-101
The percent of patients who are seizure free during the entire Treatment Period
Time frame: Treatment Period (Day 1 to Day 56) compared to placebo
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