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).
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
600
Rimegepant 75 mg, 50 mg or 35 mg ODT
The frequency and severity of on-treatment and treatment-emergent adverse events, serious adverse events, adverse events leading to discontinuation, clinically significant lab abnormalities
To evaluate the safety and tolerability of rimegepant in children and adolescents (6 to \< 18 years of age).
Time frame: 58 weeks
The frequency and severity of hepatic-related adverse events and frequency of hepatic-related adverse events leading to treatment discontinuation
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.
Time frame: 58 weeks
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Perseverance Research Center, LLC
Scottsdale, Arizona, United States
RECRUITINGPhysicians Research Group
Tempe, Arizona, United States
ACTIVE_NOT_RECRUITINGAdvanced Research Center, Inc.
Anaheim, California, United States
RECRUITINGProScience Research Group
Culver City, California, United States
RECRUITINGNeuro-Pain Medical Center
Fresno, California, United States
RECRUITINGUniversity of California San Diego, Altman Clinical and Translational Research Institute Clinic
La Jolla, California, United States
RECRUITINGAdult & Child Neurology Medical Associates
Long Beach, California, United States
RECRUITINGMemorialcare Miller Children's & Women's Hospital Long Beach
Long Beach, California, United States
RECRUITINGVelocity Clinical Research - North Hollywood
North Hollywood, California, United States
ACTIVE_NOT_RECRUITINGThe Neurology Group
Pomona, California, United States
RECRUITING...and 116 more locations