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Terminated Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT03739840

Public ClinicalTrials.gov record NCT03739840. 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 Jul 23, 2026, 2:05 AM EDT

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

Official title

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Padsevonil as Adjunctive Treatment of Focal-Onset Seizures in Adult Subjects With Drug-Resistant Epilepsy

Study identification

NCT ID
NCT03739840
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Biopharma SRL
Industry
Enrollment
232 participants

Conditions and interventions

Interventions

  • Padsevonil Drug
  • Placebo Drug

Drug

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
Mar 5, 2019
Primary completion
Sep 27, 2020
Completion
Sep 27, 2020
Last update posted
Dec 20, 2022

2019 – 2020

United States locations

U.S. sites
32
U.S. states
20
U.S. cities
32
Facility City State ZIP Site status
Ep0092 839 Chandler Arizona 85226
Ep0092 881 Tucson Arizona 85724
Ep0092 633 Carlsbad California 92011
Ep0092 629 Orange California 92868
Ep0092 845 Washington D.C. District of Columbia 20037
Ep0092 892 Bradenton Florida 34209
Ep0092 640 Hialeah Florida 33016
Ep0092 641 Jacksonville Florida 32209
Ep0092 823 Orlando Florida 32806
Ep0092 803 Honolulu Hawaii 96817
Ep0092 637 Urbana Illinois 61801
Ep0092 880 Anderson Indiana 46011
Ep0092 638 Fort Wayne Indiana 46804
Ep0092 630 Ames Iowa 50010
Ep0092 707 Lexington Kentucky 40536
Ep0092 822 Baltimore Maryland 21287
Ep0092 818 Bethesda Maryland 20817
Ep0092 889 Boston Massachusetts 02215
Ep0092 645 Golden Valley Minnesota 55422
Ep0092 644 Minneapolis Minnesota 55416
Ep0092 878 Brooklyn New York 11203
Ep0092 876 New York New York 10075
Ep0092 893 Syracuse New York 13210
Ep0092 895 The Bronx New York 10467
Ep0092 890 Chapel Hill North Carolina 27599
Ep0092 884 Charlotte North Carolina 28204
Ep0092 642 Columbus Ohio 43210
Ep0092 647 Oklahoma City Oklahoma 73106
Ep0092 882 Portland Oregon 97225
Ep0092 802 Philadelphia Pennsylvania 19107
Ep0092 829 Charlottesville Virginia 22903
Ep0092 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 109 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03739840, 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 20, 2022 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03739840 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →