A Study With Eptinezumab in Adolescents (12-17 Years) With Chronic Migraine
H. Lundbeck A/S · NCT04965675
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 12–17 · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 3
- Target enrollment
- 285
- US sites recruiting
- 9
- Study start
- June 30, 2021
- Record last updated
- October 16, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
To find out if eptinezumab is better than placebo (normal saline solution) in lowering the number of days with migraine in young people ages 12 to 17 with chronic migraine.
Being studied: Eptinezumab; Placebo
Conditions: Chronic Migraine in Children
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- The participant has a diagnosis of migraine (with or without aura) as defined by International Classification of Headache Disorders 3 (ICHD-3) guidelines with history of chronic migraine, of at least 6 months prior to the screening visit.
- During the 28-day screening period, the participant must adequately complete the headache eDiary on at least 23 of the 28 days following the screening visit.
- During the 28-day screening period, the participant must have ≥15 to ≤26 headache days, of which at least 8 are migraine days as documented in the eDiary.
Exclusion Criteria
- The participant has previously been randomised in this study and exposed to eptinezumab.
- The participant has been exposed to any monoclonal antibody treatment (including exposure in a study) \<6 months prior to the screening visit.
- The participant has been exposed to another calcitonin gene-related peptide (CGRP) antibody (including exposure in a study investigating a CGRP antibody) \<6 months prior to the screening visit.
- The participant has a history or diagnosis of complicated migraine (ICHD-3 version, 2018), chronic tension-type headache, hypnic headache, cluster headache, hemicrania continua, new daily persistent headache, or unusual migraine subtypes such as hemiplegic migraine (sporadic and familial), migraine with brainstem aura, ophthalmoplegic migraine, or migraine with neurological accompaniments that are not typical of migraine aura (diplopia, altered consciousness, or long duration; for example >60 minutes).
Recruiting US locations
New England Institute for Clinical Research (NEICR) - Stamford
Stamford, CT 06905-1206
NW FL Clinical Research Group, LLC
Gulf Breeze, FL 32561-4495
AGA Clinical Trials
Hialeah, FL 33012-3407
University of South Florida (USF) - Tampa Campus
Tampa, FL 33620
UK HealthCare-Kentucky Clinic
Lexington, KY 40536
Cincinnati Children's Hospital Medical Center-Burnet Campus
Cincinnati, OH 45229-3026
Road Runner Research (RRR)
San Antonio, TX 78249-3539
Children's Specialty Group (CSG)
Norfolk, VA 23510-1021
Marshall Health-Marshall University Medical Center
Huntington, WV 25701-3656
Study contacts (from the official record)
- Email contact via H. Lundbeck A/S · +45 36301311 · HQ_Medinfo@Lundbeck.com
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