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A Study to Test the Long-term Safety and Tolerability of Brivaracetam in Study Participants With Childhood Absence Epilepsy or Juvenile Absence Epilepsy

Active, not recruiting · Phase 3 · NCT06315322

Conditions: Childhood Absence Epilepsy, Juvenile Absence Epilepsy

At a glance

Research payments reported, 2025
$242,900
U.S. investigators named
6
Sites paid
6
Planned or actual enrollment
70

About the trial

Sponsor
UCB Biopharma SRL
Tested
Brivaracetam Film-coated tablet (drug), Brivaracetam oral solution (drug)
Dates
Started 2024-07-10; completion 2029-11-16
Results posted
Not yet

The purpose of the study is to investigate the long-term safety and tolerability of brivaracetam in study participants with childhood absence epilepsy or juvenile absence epilepsy.

From ClinicalTrials.gov, last updated 2026-08-27. Full record, eligibility and contacts (opens in a new tab)

Industry funding

UCB SA reported $242,900 in research payments for this study in 2025 (6 payments).

Products named: Briviact

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.