Efficacy and Safety Study of Rimegepant for the Preventative Treatment of Migraine in Pediatric Subjects

Description

The purpose of this study is to compare the efficacy and safety of rimegepant to placebo as a preventative treatment for migraine in children and adolescents ≥ 6 to \<18 years with episodic migraine.

Conditions

Migraine

Study Overview

Study Details

Study overview

The purpose of this study is to compare the efficacy and safety of rimegepant to placebo as a preventative treatment for migraine in children and adolescents ≥ 6 to \<18 years with episodic migraine.

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

Efficacy and Safety Study of Rimegepant for the Preventative Treatment of Migraine in Pediatric Subjects

Condition
Migraine
Intervention / Treatment

-

Contacts and Locations

Fort Smith

The Belinga Clinic, Fort Smith, Arkansas, United States, 72901

Fort Smith

The Belinga Clinic, Fort Smith, Arkansas, United States, 72901

Hawthorne

Advanced Investigative Medicine, Inc., Hawthorne, California, United States, 90250

La Mesa

Velocity Clinical Research San Diego, La Mesa, California, United States, 91942

Walnut Creek

Clinical Research of California, Walnut Creek, California, United States, 94598

Colorado Springs

Colorado Springs Neurological Associates, Colorado Springs, Colorado, United States, 80907

Fort Collins

Advanced Neurosciences Research, LLC, Fort Collins, Colorado, United States, 80528

Washington

Meridian Clinical Research, LLC, Washington, District of Columbia, United States, 20016

Bradenton

Synergy Healthcare, Bradenton, Florida, United States, 34208

Clermont

Vertex Research Group, Clermont, Florida, United States, 34711

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Subject has at least a 6 month history of migraine (with or without aura) and including the following:
  • 1. 14 or less headache days per month during the 3 month period prior to the Screening Visit
  • 2. 6 or more migraine days during the Observation Period
  • 3. 14 or less headache days during the Observation Period
  • 4. Pediatric Migraine Disability Assessment Scale (PedMIDAS) Disability Score of \>10 to ≤50, indicating mild (score of 11 to 30) or moderate (score of 31 to 50) disruption in daily activities, as assessed at the Baseline (Randomization) Visit
  • 5. Ability to verbally distinguish migraine attacks from tension/cluster or other types of headaches
  • 6. Migraine attacks, on average, lasting 4 - 72 hours if untreated
  • 7. Subjects on prophylactic migraine medication are permitted to remain on therapy if the dose has been stable for at least 3 months (12 weeks) prior to the Screening Phase, and the dose is not expected to change during the course of the study. 2) Male and female subjects ≥ 6 to \<18 years; subjects must be less than 18 at the time of signing assent / consent.
  • 1. Subjects with a history of basilar migraine, cluster headaches, or hemiplegic migraine
  • 2. The subject has a continuous migraine (defined as an unrelenting headache) within 1 month prior to Screening Visit.
  • 3. The subject has a history or diagnosis of complications of migraine
  • 4. The subject has a confounding and clinically significant pain syndrome that may interfere with the subject's ability to participate in this study.
  • 5. The subject has any current psychiatric condition that is uncontrolled and/or untreated for a minimum of 6 months prior to the Screening Visit. Subjects with a lifetime history of psychosis and/or mania are excluded.
  • 6. History of suicidal behavior or the subject is at risk of self-harm or harm to others.
  • 7. History of major psychiatric disorder.
  • 8. The subject has a current diagnosis or history of substance abuse
  • 9. The subject has a history of moderate or severe head trauma or other neurological disorder (including seizure disorder) or systemic medical disease that is, in the investigator's opinion, likely to affect central nervous system functioning.

Ages Eligible for Study

6 Years to 17 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Pfizer,

Pfizer CT.gov Call Center, STUDY_DIRECTOR, Pfizer

Study Record Dates

2027-04-29