RECRUITING

Qudexy XR for the Prevention of Migraine in Children 6 to 11 Years Old

Description

A Phase 4 study to evaluate Qudexy XR for the prevention of migraine in children 6 to 11 years of age.

Study Overview

Study Details

Study overview

A Phase 4 study to evaluate Qudexy XR for the prevention of migraine in children 6 to 11 years of age.

A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 4 Study to Evaluate the Efficacy and Safety of Qudexy(R) XR in the Prevention of Migraine in Children 6 to 11 Years of Age

Qudexy XR for the Prevention of Migraine in Children 6 to 11 Years Old

Condition
Migraine Disorders
Intervention / Treatment

-

Contacts and Locations

Birmingham

Upsher-Smith Clinical Trial Site #5, Birmingham, Alabama, United States, 35205

La Jolla

Upsher-Smith Clinical Trial Site #15, La Jolla, California, United States, 92093

Aurora

Upsher-Smith Clinical Trials Site #3, Aurora, Colorado, United States, 80045

Stamford

Upsher-Smith Clinical Trial Site #1, Stamford, Connecticut, United States, 06901

Loxahatchee Groves

Upsher-Smith Clinical Trial Site #12, Loxahatchee Groves, Florida, United States, 33470

Orlando

Upsher-Smith Clinical Trial Site #8, Orlando, Florida, United States, 32789

Tampa

Upsher-Smith Clinical Trial Site #14, Tampa, Florida, United States, 33620

Ann Arbor

Upsher-Smith Clinical Trial Site #2, Ann Arbor, Michigan, United States, 48104

Jackson

Upsher-Smith Clinical Trial Site #11, Jackson, Mississippi, United States, 39216

Bridgeton

Upsher-Smith Clinical Trial Site #10, Bridgeton, Missouri, United States, 63044

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 is a female or male 6 to 11 years of age, inclusive, at Visit 1 (Screening)
  • 2. Subject weighs at least 17.0 kg and less than 50.0 kg at Visit 1 (Screening) based on 95 percentile weight for the age range.11
  • 3. Subject has at least a 6-month history of headaches consistent with a diagnosis of migraine with or without aura (International Classification of Headache Disorders, 3rd Edition \[ICHD 3\]).
  • 4. Subject had ≥8 self-reported headache days in the 28 days prior to Screening.
  • 5. Subject has a PedMIDAS score \>10, indicating at least mild disruption in daily activities, and \<140, indicating extreme disability that may require more comprehensive, multi component therapy.
  • 1. Subject has continuous migraines, defined as an unrelenting headache for a 28-day period.
  • 2. Subject is currently receiving treatment or has used Botulinum toxin (Botox®) within 3 months prior to Visit 1 (Screening).
  • 3. Subject is currently receiving migraine prevention medication and has initiated or changed the dose within 28 days of Screening or is unwilling to avoid making a change during the duration of the study.
  • 4. Subject has previously failed an adequate trial of topiramate (at least 3 months duration at a clinically appropriate dose) for prophylaxis of migraine headache due to lack of efficacy or AEs.
  • 5. Subject has previously failed an adequate trial of \>3 migraine preventative medications.
  • 6. Subject has a known history of allergic reaction to topiramate or any excipient in Qudexy XR.
  • 7. Subject has a diagnosis or history of disease that may interfere with safety or evaluation of the study drug.
  • 8. Subject is currently using an investigational drug or device or has used such within 30 days prior to Visit 1.
  • 9. Subject has begun menses and any of the following:
  • 1. Subject has tested positive for pregnancy; OR
  • 2. Subject is pregnant, planning pregnancy, or lactating; OR
  • 3. Subject is taking an oral hormonal contraceptive (either combined \[estrogen and progestogen containing\] or progestogen-only) and is unable or unwilling to switch to an alternative highly effective contraceptive method.

Ages Eligible for Study

6 Years to 11 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Upsher-Smith Laboratories,

Study Record Dates

2026-09