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RecruitingPediatric Migraine

Randomized Study in Children and Adolescents With Migraine: Acute Treatment

Eligible age

6–17 yrs

Accepts

All genders

Locations

38 states

Healthy volunteers

No

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About this study

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.

Sponsor: Pfizer

You may qualify if…

  • 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.

You may not qualify if…

  • 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).

Where it's recruiting

Alabama

Birmingham

Arizona

Scottsdale · Tempe

California

Anaheim · Costa Mesa · Culver City · Fountain Valley

Colorado

Aurora · Colorado Springs

Connecticut

Cromwell · Hartford · Stamford

Delaware

Wilmington

District of Columbia

Washington D.C.

Florida

Apopka · Cutler Bay · DeLand · Gainesville

Georgia

Atlanta · Brunswick · Decatur

Illinois

Chicago · Naperville

Indiana

Westfield

Iowa

Sioux City · West Des Moines

Source: ClinicalTrials.gov · NCT04649242 · last updated 2026-06-16

Randomized Study in Children and Adolescents With Migraine: Acute Trea · TrialPath