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Keep this study
Lead
Praxis Precision Medicines
An open label extension clinical trial to assess the safety and tolerability of vormatrigine in adults with focal or primary generalized tonic-clonic seizures.
Age
18–85
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Participant who completed an eligible clinical trial (unless agreed by the sponsor medical monitor), including PRAX-628-212, PRAX-628-321 or other vormatrigine trials, or participant who has received vormatrigine outside of an eligible clinical trial (such as an expanded access program)
Participant who had adequate seizure diary and vormatrigine adherence and had been otherwise adherent to the study procedures in the opinion of the investigator unless deemed unacceptable by sponsor
You may not be if
Participant who withdrew or discontinued treatment from the treatment period of an eligible clinical trial unless deemed acceptable by the sponsor
Participant who plans to enter another interventional investigational study or is on any prohibited medication
Participant who is pregnant, lactating or planning to become pregnant
Participant who is ineligible for the extension clinical trial in the view of the investigator
