Biohaven Therapeutics Ltd.
A study to determine if BHV- 7000 is safe and tolerable in adults with refractory focal onset epilepsy
Key Inclusion Criteria: * Subjects who completed the double-blind phase (DBP) of prior parent study, BHV7000-302 or BHV7000-303. * (FOCBP) Females of Child Bearing Potential must have a negative urine pregnancy test at the Baseline/Day 0 visit Key Exclusion Criteria: * Any condition, such as an ongoing AE with/without sequelae, or is poorly tolerating IP in the double-blind phase of the parent study, that would interfere with the subject's ability to comply with study instructions, place the subject at unacceptable risk, and/or confound the interpretation of safety or efficacy data from the…
BHV-7000 50 mg. Participants will take open-label investigational product (IP) once daily
BHV-7000 75 mg. Participants will take open-label investigational product (IP) once daily