NCT04748601PHASE4Recruiting
Qudexy XR for the Prevention of Migraine in Children 6 to 11 Years Old
Upsher-Smith Laboratories
Start Date
2/19/2021
Completion Date
9/1/2026
Summary
A Phase 4 study to evaluate Qudexy XR for the prevention of migraine in children 6 to 11 years of age.
Eligibility Criteria
Age Range: 6 years to 11 years
Inclusion 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.
Exclusion Criteria:
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.
Interventions
DRUG
Qudexy XR
DRUG
Placebo
Conditions
Migraine Disorders
Locations
Upsher-Smith Clinical Trial Site #5
Birmingham, Alabama 35205
United States
Upsher-Smith Clinical Trial Site #15
La Jolla, California 92093
United States
Upsher-Smith Clinical Trials Site #3
Aurora, Colorado 80045
United States
Upsher-Smith Clinical Trial Site #1
Stamford, Connecticut 06901
United States
Upsher-Smith Clinical Trial Site #12
Loxahatchee Groves, Florida 33470
United States
Upsher-Smith Clinical Trial Site #8
Orlando, Florida 32789
United States
Upsher-Smith Clinical Trial Site #14
Tampa, Florida 33620
United States
Upsher-Smith Clinical Trial Site #2
Ann Arbor, Michigan 48104
United States
Upsher-Smith Clinical Trial Site #11
Jackson, Mississippi 39216
United States
Upsher-Smith Clinical Trial Site #10
Bridgeton, Missouri 63044
United States
Upsher-Smith Clinical Trial Site #4
Cincinnati, Ohio 45229
United States
Upsher-Smith Clinical Trial Site #6
Portland, Oregon 97239
United States
Upsher-Smith Clinical Trials Site #7
Springfield, Oregon 97477
United States
Upsher-Smith Clinical Trial Site #13
McAllen, Texas 78503
United States
Upsher-Smith Clinical Trial Site #9
Huntington, West Virginia 25701
United States