Recruiting

Qudexy XR

Sponsor:

Upsher-Smith Laboratories

Code:

NCT04748601

Conditions

Migraine Disorders

Eligibility Criteria

Sex: All

Age: 6 - 11

Healthy Volunteers: Not accepted

Interventions

Qudexy XR

Placebo

Study Details

Brief summary:

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

Conditions

Migraine Disorders

Study ID

NCT04748601

Start date

Feb 19, 2021

Status verified date

Jan, 2025

Completion date

Sep, 2026

Anticipated

Primary completion date

Sep, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 6 - 11

Healthy Volunteers: Not accepted

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.

Study Design

Enrollment

132 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

placebo comparator: Placebo

experimental: Qudexy XR

Interventions

Qudexy XR

Extended-Release Capsule

Placebo

Qudexy XR Matching capsules

Primary outcome measure

  • Change from Baseline (last 28 days Run-In Period) in the monthly number of headache days during the 8-week Maintenance Period based on the diary. [ Time Frame: 16 Weeks ]

Central Contacts and Locations

Central contacts

Locations

Upsher-Smith Clinical Trial Site #15

Recruiting

La Jolla, California, United States, 92093

Upsher-Smith Clinical Trial Site #14

Recruiting

Tampa, Florida, United States, 33620

Upsher-Smith Clinical Trial Site #4

Recruiting

Cincinnati, Ohio, United States, 45229

Upsher-Smith Clinical Trial Site #6

Recruiting

Portland, Oregon, United States, 97239

Upsher-Smith Clinical Trials Site #7

Recruiting

Springfield, Oregon, United States, 97477

Upsher-Smith Clinical Trial Site #9

Recruiting

Huntington, West Virginia, United States, 25701

More Information

Sponsor

Upsher-Smith Laboratories

Last update posted

Jan 27, 2025

Last verified

Jan, 2025

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Upsher-Smith Laboratories on 2025-01-27.