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NCT07219407 · ClinicalTrials.gov registry record · Phase 2

A Long-term Study of the Safety and Effectiveness of RAP-219 in Adults With Focal Onset Seizures

A Phase 2 study of Epilepsy and Focal Epilepsy, sponsored by Rapport Therapeutics.

Recruiting
Registry status
Phase 2
Development phase
30
Enrollment target
7
Study locations

NCT07219407 is a Phase 2 study of Epilepsy and Focal Epilepsy that is actively recruiting participants, run by Rapport Therapeutics. The registered enrollment target is 30 participants, below the 952-participant average among 160 other Epilepsy trials with a reported enrollment target (97% lower). The trial reports 7 study locations across 7 states.

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The verdict

NCT07219407, a Phase 2 study of Epilepsy and Focal Epilepsy, is actively recruiting participants, sponsored by Rapport Therapeutics.

RECRUITING
Registry status
Phase 2
Development phase
30 participants
Enrollment target
7
Study locations

Study Summary

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 RAP-219 Long- term safety and open-label antiseizure activity in patients with Refractory Focal Epilepsy.

Interventions

  • DRUG RAP-219

Study Locations (7)

Idaho

  • Consultants in Epilepsy and Neurology, PLLC - Boise

Minnesota

  • Mayo Clinic - Rochester

New York

  • NYU Langone Comprehensive Epilepsy Center - New York

Ohio

  • Cleveland Clinic Foundation - Cleveland

Pennsylvania

  • University of Pennsylvania - Department of Neurology - Philadelphia

Tennessee

  • Vanderbilt University Medical Center - Nashville

Texas

  • Baylor College of Medicine - Houston

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2025-12-15
Est. Completion 2028-02-03
Phase Phase 2

Sponsor

Rapport Therapeutics

5 total trials

What the Registry Record Tells You About NCT07219407

The ClinicalTrials.gov registry entry for NCT07219407 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 952-participant average among 160 other Epilepsy trials with a reported enrollment target (97% lower). The listed sponsor is Rapport Therapeutics, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 6 conditions, with Epilepsy appearing as the primary indexed condition, and to 1 intervention - of which RAP-219 is the first listed.

NCT07219407 reports 7 study locations spanning 7 distinct geographic areas - top geographies include Idaho, Minnesota, New York.

Frequently Asked Questions

What is clinical trial NCT07219407 about?

NCT07219407 is a clinical study titled "A Long-term Study of the Safety and Effectiveness of RAP-219 in Adults With Focal Onset Seizures". 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 RAP-219 Long- term safety and open-label antiseizure activity in patients with Refractory Focal Epilepsy.

What is the current status of trial NCT07219407?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2025-12-15. Estimated completion is 2028-02-03.

What conditions does trial NCT07219407 study?

This clinical trial studies the following conditions: Epilepsy, Focal Epilepsy, Seizure, Focal Seizure, Focal Onset Seizure.

What interventions are being tested in trial NCT07219407?

The interventions under investigation include: RAP-219 (DRUG).

Who is sponsoring clinical trial NCT07219407?

This trial is sponsored by Rapport Therapeutics, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07219407 being conducted?

This trial has 7 study locations across Idaho, Minnesota, New York, Ohio, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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