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NCT07287163Enrolling by invitationPhase 3

Clinical Trial of Vormatrigine in Adult Patients With Epilepsy

Open Label Extension Clinical Trial of Vormatrigine in Adult Patients With Epilepsy

Source: ClinicalTrials.gov · Last updated 3 Aug 2026

Brief summary (registry, in English)

Open Label Extension Clinical Trial of Vormatrigine in Adult Patients with Epilepsy

Status (registry)
Enrolling by invitation
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
700 (estimated)
First submitted
11 Dec 2025
Start date
27 Oct 2025
Primary completion date
31 May 2028
Lead sponsor
Praxis Precision Medicines
Diseases
Epilepsy
NCT number
NCT07287163

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 700
  • From 27 Oct 2025 to the primary completion date, 31 May 2028
  • 36 sites in 6 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participant who plans to enter another interventional investigational study or is on any prohibited medication

Other

  • Participant who withdrew or discontinued treatment from the treatment period of an eligible clinical trial unless deemed acceptable by the sponsor
  • 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

Who the study is looking for

  • 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

Age in the registry: 18 years to 85 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (36)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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Coordinator of this site? Confirm its status
Porto AlegreBrazilUnknown status
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São José do Rio PretoBrazilUnknown status
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BielefeldGermanyUnknown status
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TübingenGermanyUnknown status
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BarcelonaSpainUnknown status
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MadridSpainUnknown status
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MálagaSpainUnknown status
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TerrassaSpainUnknown status
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ValenciaSpainUnknown status
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Bosisio PariniItalyUnknown status
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MilanItalyUnknown status
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NaplesItalyUnknown status
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PaviaItalyUnknown status
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PisaItalyUnknown status
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PonderanoItalyUnknown status
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PozzilliItalyUnknown status
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RomaItalyUnknown status
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BydgoszczPolandUnknown status
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KatowicePolandUnknown status
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LublinPolandUnknown status
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WarsawPolandUnknown status
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AmherstUnited StatesUnknown status
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BethesdaUnited StatesUnknown status
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ChesterfieldUnited StatesUnknown status
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El PasoUnited StatesUnknown status
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HackensackUnited StatesUnknown status
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HoustonUnited StatesUnknown status
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LafayetteUnited StatesUnknown status
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MiamiUnited StatesUnknown status
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Miami LakesUnited StatesUnknown status
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MiddletownUnited StatesUnknown status
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NaplesUnited StatesUnknown status
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New YorkUnited StatesUnknown status
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Niagara FallsUnited StatesUnknown status
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PhiladelphiaUnited StatesUnknown status
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PlymouthUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.