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Terminated Phase 2 Interventional Results available

Study to Test the Safety and Efficacy of Padsevonil as Adjunctive Treatment of Focal-onset Seizures in Adult Subjects With Drug-resistant Epilepsy

ClinicalTrials.gov ID: NCT03370120

Public ClinicalTrials.gov record NCT03370120. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 7, 2026, 2:25 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label, Multicenter, Extension Study to Evaluate the Safety and Efficacy of Padsevonil as Adjunctive Treatment of Focal-Onset Seizures in Adult Subjects With Drug-Resistant Epilepsy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of the study is to evaluate the long-term safety and tolerability of Padsevonil administered at individualized doses as adjunctive treatment for subjects with drug-resistant epilepsy.

Study identification

NCT ID
NCT03370120
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
UCB Biopharma SRL
Industry
Enrollment
406 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 26, 2018
Primary completion
Dec 10, 2020
Completion
Dec 10, 2020
Last update posted
Dec 28, 2021

2018 – 2020

United States locations

U.S. sites
25
U.S. states
16
U.S. cities
24
Facility City State ZIP Site status
Ep0093 839 Chandler Arizona 85226
Ep0093 815 La Jolla California 92037
Ep0093 801 San Francisco California 94115
Ep0093 803 Honolulu Hawaii 96817
Ep0093 638 Fort Wayne Indiana 46804
Ep0093 707 Lexington Kentucky 40536
Ep0093 822 Baltimore Maryland 21287
Ep0093 818 Bethesda Maryland 20817
Ep0093 889 Boston Massachusetts 02215
Ep0093 645 Golden Valley Minnesota 55422
Ep0093 817 Saint Paul Minnesota 55102
Ep0093 806 Hackensack New Jersey 07601
Ep0093 893 Syracuse New York 13210
Ep0093 895 The Bronx New York 10467-24 01
Ep0093 890 Chapel Hill North Carolina 27514
Ep0093 884 Charlotte North Carolina 28204
Ep0093 642 Columbia Ohio 43210
Ep0093 802 Philadelphia Pennsylvania 19107
Ep0093 838 Cordova Tennessee 38018
Ep0093 835 Nashville Tennessee 37232
Ep0093 805 Austin Texas 78701
Ep0093 844 Austin Texas 78758
Ep0093 824 Round Rock Texas 78681
Ep0093 870 San Antonio Texas 78229
Ep0093 639 Renton Washington 98055

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 131 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03370120, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 28, 2021 · Synced Sep 7, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03370120 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →