Rapport Extension Study

Enrolling By Invitation
99 years or below
All
Phase N/A
1 participants needed
1 Location

Brief description of study

All objectives are listed in section 3 of the protocol, but the primary objective is to evaluate the long-term safety of RAP-219 in participants with focal onset seizures. The primary endpoint is the incidence of treatment-emergent adverse events (TEAEs). The secondary objectives and their associated endpoints can be found in section 3 of the protocol.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Medical Research
  • Age: 99 years or below
  • Gender: All

TBD

Updated on 02 Apr 2026. Study ID: 25-1498
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Study is selecting its participants from a population, or group of people, decided on by the researchers in advance.

Contact Office of Clinical Research