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NCT06377930CompletedPhase 2

Study Evaluating the Safety and Efficacy of RAP-219 in Adult Participants With Refractory Focal Epilepsy

A Phase 2A, Multicenter, Open-label Study Evaluating the Safety and Efficacy of RAP-219 in Adult Participants With Refractory Focal Epilepsy

Source: ClinicalTrials.gov · Last updated 5 Feb 2026

Brief summary (registry, in English)

This is a clinical research study for an investigational drug called RAP-219 in patients with Refractory Focal Epilepsy. This study is being conducted to determine if RAP-219 works and is safe in patients with Refractory Focal Epilepsy.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
30 (actual)
First submitted
17 Apr 2024
Start date
10 Oct 2024
Primary completion date
26 Sept 2025
Lead sponsor
Rapport Therapeutics Inc.
Diseases
Epilepsy
NCT number
NCT06377930

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 30
  • From 10 Oct 2024 to the primary completion date, 26 Sept 2025
  • 12 sites in 1 country
  • 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

  • Participants who have had epilepsy surgery within the last 12 months before screening

Other illness

  • Participants with generalized onset seizures in the past 10 years
  • History of status epilepticus while on antiseizure medications within 2 years of screening

Other

  • Individuals of reproductive potential who do not agree to simultaneously use two effective birth-control methods

Who the study is looking for

  • Medically refractory focal epilepsy with an implanted responsive neurostimulator device placed correctly in a seizure onset zone that meet several device-related criteria and demonstrated history of compliance with interrogation of the RNS device and upload of data
  • If currently treated with antiseizure medications, up to a maximum of 4 concomitant mediations are allowed
  • At least 1 clinical seizure during the 8-week retrospective eligibility period
  • Participants in otherwise good health as determined by the investigator
  • Willing and able to adhere to all aspects of the protocol
  • A demonstrated history of compliance with interrogation of the RNS device and upload of data before screening

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (12)

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

SiteCityCountrySite status
Consultants in Epilepsy and Neurology PLLC
Coordinator of this site? Confirm its status
BoiseUnited StatesUnknown status
Cleveland Clinic Foundation
Coordinator of this site? Confirm its status
ClevelandUnited StatesUnknown status
Baylor College of Medicine
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
University of Texas Health Science Center, Houston
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
IU Health Neuroscience Center, Goodman Hall
Coordinator of this site? Confirm its status
IndianapolisUnited StatesUnknown status
The University of Kansas Medical Center Epilepsy Clinic
Coordinator of this site? Confirm its status
Kansas CityUnited StatesUnknown status
Vanderbilt University Medical Center
Coordinator of this site? Confirm its status
NashvilleUnited StatesUnknown status
Yale University
Coordinator of this site? Confirm its status
New HavenUnited StatesUnknown status
NYU Langone Comprehensive Epilepsy Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
University of Pennsylvania - Department of Neurology
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
Thomas Jefferson University
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
Mayo Clinic
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status

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