Rimegepant (PF-07899801)
DrugRimegepant 75 mg, 50 mg or 35 mg ODT
NCT Number: NCT04743141
The purpose of this study is to test the long-term safety of rimegepant in the acute treatment of migraine in children and adolescents (≥ 6 to < 18 years of age).
Interested in participating?
Request Info6 year–17 year
All sexes
Interventional
Phase 3
NZOZ Wielospecjalistyczna Poradnia Lekarska SYNAPSIS, Lech Szczechowski, Katowice, Poland
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Rimegepant 75 mg, 50 mg or 35 mg ODT
Time frame: 58 weeks
To evaluate the safety and tolerability of rimegepant in children and adolescents (6 to < 18 years of age).
Time frame: 58 weeks
To evaluate the frequency and severity of hepatic-related adverse events and the frequency of hepatic-related treatment discontinuations in children and adolescents (6 to less than 18 years of age) treated with rimegepant.
Contact information is provided by the study sponsor or research team.
Pfizer
Industry
Phase 3, Multicenter, Open-label Study to Assess the Long-term Safety and Tolerability of Rimegepant for the Acute Treatment of Migraine (With or Without Aura) in Children and Adolescents ≥ 6 to < 18 Years of Age
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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