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A Study to Test the Long-term Safety, Tolerability and Efficacy of Brivaracetam in Study Participants 2 to 26 Years of Age With Childhood Absence Epilepsy or Juvenile Absence Epilepsy

Completed · Phase 3 · NCT05109234

Conditions: Childhood Absence Epilepsy, Juvenile Absence Epilepsy

At a glance

Research payments reported, 2025
$126,904
U.S. investigators named
6
Sites paid
7
Planned or actual enrollment
84

About the trial

Sponsor
UCB Biopharma SRL
Tested
Brivaracetam Film-coated tablet (drug), Brivaracetam oral solution (drug)
Dates
Started 2022-03-30; completion 2025-03-18
Results posted
Yes

The purpose of the study is to investigate the long-term safety, tolerability and efficacy of brivaracetam in pediatric study participants with childhood absence epilepsy (CAE) or juvenile absence epilepsy (JAE).

From ClinicalTrials.gov, last updated 2025-10-22. Full record, eligibility and contacts (opens in a new tab)

Industry funding

UCB SA reported $126,904 in research payments for this study in 2025 (7 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.