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Terminated Phase 3 Interventional Results available

A Long-term Safety and Tolerability Study of USL261 in Patients With Seizure Clusters

ClinicalTrials.gov ID: NCT02161185

Public ClinicalTrials.gov record NCT02161185. 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 Oct 23, 2026, 6:18 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

An Open-Label Safety Study of USL261 in the Outpatient Treatment of Adolescent and Adult Subjects With Seizure Clusters

Brief summary

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

The purpose of this study is to examine the long-term safety and tolerability of USL261 in the treatment of seizure clusters.

Study identification

NCT ID
NCT02161185
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Biopharma S.P.R.L.
Industry
Enrollment
7 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
12 Years to 65 Years
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
May 2014 (Type not available)
Primary completion
May 2015 (Actual)
Completion
May 2015 (Actual)
Last update posted
Oct 10, 2019

2014 – 2015

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Not listed Tucson Arizona — —
Not listed Fresno California — —
Not listed Ventura California — —
Not listed Aurora Colorado — —
Not listed Port Charlotte Florida — —
Not listed Tampa Florida — —
Not listed Boise Idaho — —
Not listed Chicago Illinois — —
Not listed Lexington Kentucky — —
Not listed Saint Paul Minnesota — —
Not listed Reno Nevada — —
Not listed Philadelphia Pennsylvania — —
Not listed Nashville Tennessee — —
Not listed Dallas Texas — —
Not listed Houston Texas — —
Not listed San Antonio Texas — —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02161185, 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 Oct 10, 2019 · Synced Oct 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 public registry record, listed eligibility criteria, and available contact information for NCT02161185 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →