Randomized Study in Children and Adolescents With Migraine: Acute Treatment

Description

The purpose of this study is to test the safety and efficacy of BHV-3000 versus placebo in the acute treatment of moderate or severe migraine in children and adolescents.

Conditions

Pediatric Migraine

Study Overview

Study Details

Study overview

The purpose of this study is to test the safety and efficacy of BHV-3000 versus placebo in the acute treatment of moderate or severe migraine in children and adolescents.

Phase 3, Multicenter, Randomized, Double-blind, Group Sequential, Placebo-controlled Study to Assess Efficacy and Safety of Rimegepant for the Treatment of Migraine (With or Without Aura) in Children and Adolescents ≥ 6 to < 18 Years of Age

Randomized Study in Children and Adolescents With Migraine: Acute Treatment

Condition
Pediatric Migraine
Intervention / Treatment

-

Contacts and Locations

Birmingham

Accel Research Sites-Neurology and Neurodiagnostics of Alabama, LLC, Birmingham, Alabama, United States, 35244

Phoenix

Phoenix Children's Hospital, Phoenix, Arizona, United States, 85016

Scottsdale

Perseverance Research Center, LLC, Scottsdale, Arizona, United States, 85254

Tempe

Physicians Research Group, Tempe, Arizona, United States, 85284

Anaheim

Advanced Research Center, Inc., Anaheim, California, United States, 92805

Banning

Velocity Clinical Research, Banning, Banning, California, United States, 92220

Culver City

ProScience Research Group, Culver City, California, United States, 90230

Fresno

Neuro-Pain Medical Center, Fresno, California, United States, 93710

La Jolla

University of California, San Diego Altman Clinical Translational Research Institute, La Jolla, California, United States, 92037

Lafayette

Sunwise Clinical Research, LLC, Lafayette, California, United States, 94549

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. History of migraine (with or without aura) for \> 6 months before Screening according to the IHS Classification ICHD-319 specifications for pediatric migraine. History may be verified using both medical records and recall by the participant and/or participant's parent(s)/legal representative(s).
  • 2. History of 1 to 8 moderate or severe attacks per month during the 2 months prior to enrollment, with attacks lasting \> 3 hours without treatment, and attacks occurring at intervals \> 24 hours.
  • 3. Prophylactic migraine medication are permitted if the dose has been stable for at least 12 weeks prior to the Baseline Visit, and the dose is not expected to change during the course of the study.
  • 1. Participants may remain on one (1) medication with possible migraine prophylactic effects, excluding CGRP antagonists \[biologic or small molecule\], during the treatment phases.
  • 2. Concomitant use of a CGRP antagonist, such as erenumab or fremanezumab, is prohibited.
  • 3. Previously discontinued prophylactic migraine medication must have done so at least 90 days prior to the Screening Visit.
  • 4. Verbally distinguish between migraine and other types of headaches.
  • 5. Participants must have a weight \> 40 kg at the Screening Visit.
  • 6. Adequate venous access for blood sampling.
  • 7. Male and female participants ≥ 6 to \< 18 years of age (participants must not reach their 18th birthday during the study).
  • 1. History of cluster headache or hemiplegic migraine headache.
  • 2. Confounding and clinically significant pain syndrome that may interfere with the participant's ability to participate in this study.
  • 3. Current psychiatric condition that is uncontrolled and/or untreated for a minimum of 6 months prior to the Screening Visit. Participants with a lifetime history of psychosis and/or mania.
  • 4. History of suicidal behavior or major psychiatric disorder.
  • 5. Current diagnosis or history of substance abuse; positive drug test at Screening.
  • 6. History of moderate or severe head trauma or other neurological disorder (including seizure disorder) or systemic medical disease that is likely to affect central nervous system functioning.
  • 7. Recent or planned surgery, requiring general anesthesia, \<8 weeks prior to the Screening Visit.
  • 8. Participant has had gastrointestinal surgery that interferes with physiological absorption and motility (i.e., gastric bypass, duodenectomy, or gastric banding).
  • 9. Current diagnosis of viral hepatitis or a history of liver disease.
  • 10. Conditions considered clinically relevant in the context of the study such as uncontrolled hypertension (high blood pressure), diabetes, a life-threatening allergy

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

2029-01-09