- About the Study
- The purpose of this study is to evaluate how safe and effective the investigational drug ubrogepant is in the acute treatment of migraine in children and adolescents.
- What does the study involve?
- Ubrogepant is approved for the acute treatment of migraine in adults but has not been studied in children 6-17 years of age. The study will include 2 cohorts of participants - PK Cohort for children 6 to 11 years of age and the Main safety and efficacy study for children 6 to 17 years of age. There will also be a possibility for your child to participate in the long-term extension study, after completion of the main safety and efficacy study, where they will receive Ubrogepant for a year.
- Who can participate?
- Your child may qualify for the study if they are between the ages of 6-17 years old, have experienced migraines for at least 6 months, and experienced between 1 and 14 migraine attacks per month.
- Where is the study taking place?
- The study is being conducted at our Hollywood, Weston, and Boynton offices.
- Is compensation provided?
- Yes