Under construction – not a live service
Sign in
Taking people in United StatesPhase 3

RAP-219 for Adults With Focal Seizures

Tests RAP-219 for reducing seizures in adults with focal epilepsy.

Plain-language title generated from the registry record
Registry title: Study Evaluating the Efficacy and Safety of RAP-219 in Adult Participants With Focal Seizures FOCUS-1

Key facts

Where
Asheville, Atlanta, Bethesda, Birmingham, Boise, Cleveland, Fort Wayne, Gulf Breeze, Hackensack, Livingston, New York, Palmdale, Philadelphia, Richmond, Springfield, and The Bronx, United StatesSee the 16 sites
Phase
Phase 3

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 75 years old?

Source: NCT07563881, who can take part

Where in United States

  • Asheville Neurology SpecialistsAsheville, United StatesTaking people
  • Emory Brain Health CenterAtlanta, United StatesTaking people
  • Mid-Atlantic Epilepsy and Sleep CenterBethesda, United StatesTaking people
  • University of Alabama at BirminghamBirmingham, United StatesTaking people
  • Consultants in Epilepsy & Neurology, PLLCBoise, United StatesTaking people
  • Cleveland ClinicCleveland, United StatesTaking people
  • Indiana University Health Fort Wayne NeurologyFort Wayne, United StatesTaking people
  • Panhandle Research and Medical Clinic, LLCGulf Breeze, United StatesTaking people
  • Northeast Regional Epilepsy GroupHackensack, United StatesTaking people
  • Institute of Neurology and Neurosurgery at St. BarnabasLivingston, United StatesTaking people
  • NYU Langone Health - Comprehensive Epilepsy CenterNew York, United StatesTaking people
  • Amicis Research CenterPalmdale, United StatesTaking people
  • Thomas Jefferson UniversityPhiladelphia, United StatesTaking people
  • Neurological AssociatesRichmond, United StatesTaking people
  • Southern Illinois University Neurology ClinicSpringfield, United StatesTaking people
  • Montefiore Medical CenterThe Bronx, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Rapport Therapeutics Inc.
Trial code
NCT07563881
Record updated
6 November 2026
Original description
This is a clinical research study for an investigational drug called RAP-219 in adult participants with focal seizures. This study is being conducted to determine if RAP-219 is safe and effective in reducing focal seizure frequency.Read full original descriptionShow less

A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of RAP-219 in Adult Participants With Focal Seizures

This is a clinical research study for an investigational drug called RAP-219 in adult participants with focal seizures. This study is being conducted to determine if RAP-219 is safe and effective in reducing focal seizure frequency.

Inclusion: Age 18 - 75; BMI 18-45 kg/m2; Diagnosis of focal epilepsy for ≥24 months prior to Visit 1; Report from at least 1 brain MRI or CT scan and 1 EEG study, each completed within 10 years prior to Visit 1, consistent with focal epilepsy diagnosis; Concomitant use of between 1 and 3, inclusive, antiseizure medication(s) ASM(s) as maintenance, not including rescue or pro re nata (PRN) ASMs; Ability to keep accurate daily focal seizure records using an e-diary.

Exclusion: Known hypersensitivity or prior exposure to RAP-219; Anticipated need for surgery during the study period; Medical history of any of the following:; generalized epilepsy; focal preserved consciousness without observable manifestations (also known as focal aware nonmotor) as the participant's only seizure type; psychogenic nonepileptic seizure (PNES); status epilepticus or seizure clusters (when individual seizures cannot be counted) within 12 months prior to Visit 1 (Day -56); epilepsy surgery within 12 months prior to Visit 1 (Day -56); Participation in another clinical study of an investigational product within 12 weeks or 5 half-lives of this other investigational product; Unstable or uncontrolled serious medical, neurologic (other than focal epilepsy), or psychiatric condition that is ongoing or considered likely to recur.

ClinicalTrials.gov NCT07563881