WHO ICTRP trial

A study to test the long-term safety, tolerability and efficacy of brivaracetam…

EUCTR2020-002769-33-HU · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2020-002769-33-HU
Public title A study to test the long-term safety, tolerability and efficacy of brivaracetam in study participants 2 to 26 years of age with with childhood absence epilepsy or juvenile absence epilepsy.
Scientific title A Multicenter, Open-Label, Single-Arm Study to Evaluate 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
Primary sponsor UCB Biopharma SRL
Registry EU Clinical Trials Register
Recruitment status Not Recruiting
Study type Interventional clinical trial of medicinal product
Phase Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no
Countries United States;Hungary;Spain;Poland;Belgium;Ukraine;Romania;Australia;Georgia;Italy
Conditions Childhood absence epilepsy (CAE) Juvenile absence epilepsy (JAE);Therapeutic area: Diseases [C] - Nervous System Diseases [C10]
Interventions Trade Name: Briviact Pharmaceutical Form: Oral solution INN or Proposed INN: BRIVARACETAM CAS Number: 357336-20-0 Current Sponsor code: BRV Other descriptive name: Briviact Concentration unit: mg/ml milligram(s)/millilitre Concentration…
Registration date Dec 29, 2020
Target size 140
Secondary IDs EP0132
Registry page clinicaltrialsregister.eu

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