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A Phase 3, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Rimegepant in Migraine Prevention in Children and Adolescents = 6 to <18 years of age
This study is looking to evaluate the safety and efficacy of the use of rimegepant in the pediatric population to treat acute migraines in patients ages = 6 to <18 old with a history of migraines.
A Randomized, Double-blind, Multicenter, Parallel-group, Phase IIIb 52 Week Study Evaluating the Efficacy and Safety of PT027 Compared with PT007 Administered As Needed in Participants 12 to < 18 Years of Age with Asthma (ACADIA)
Compare Budesonide/albuterol metered-dose inhaler with Albuterol sulfate metered-dose inhaler on the severe asthma exacerbations in adolescent participants with documented clinical diagnosis of asthma.
An Interventional, Efficacy, And Safety, Phase 3 Randomized, Double-Blind, Placebo-Controlled Study With An Open-Label Extension To Investigate Rimegepant In Migraine Prevention In Adolescents 12 To Less Than 18 Years Of Age With Chronic Migraine
The purpose of this study is to learn about the effect of a study medicine called rimegepant in adolescents who have frequent migraine attacks.
Improving Neurodevelopmental ouTcomes After Prenatal Cannabinoid in uTero Exposure (INTACT)
Pilot feasibility study to test the effectiveness of the INTACT Intervention program in improving neurodevelopmental outcomes in infants prenatally exposed to cannabinoids.
Post-approval Registry Study to Evaluate the Continued Safety and Probable Benefit of the MID-C System for 5 Years Post-Implantation in Adolescent Idiopathic Scoliosis (AIS) (MID-C)
The ApiFix MID-C System is a unidirectional expandable rod, designed to be connected unilaterally to the spine via 2 anchor points on the concave side of a scoliotic deformity above and below the apex of the major curvature to treat adolescent idiopathic scoliosis. The MID-C System is designed to act as an internal brace.

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