Chronic Migraine
Conditions
Keywords
pediatric, children, prevention, prophylaxis, headache, pediatric migraine
Brief summary
The main purpose of this study is to evaluate the efficacy and safety of galcanezumab for the preventive treatment of chronic migraine in participants 12 to 17 years of age. The primary objective is to demonstrate the superiority of galcanezumab versus placebo in the reduction of monthly migraine headache days across the 3-month double-blind treatment period.
Detailed description
The study includes a 3-month, randomized, double-blind treatment period in which participants receive either galcanezumab or placebo, followed by a 9-month open-label extension in which all participants receive galcanezumab. Enrollment in the European Union may also include participants 6 to 11 years of age.
Interventions
DRUGGalcanezumab
Administered SQ
DRUGPlacebo
Administered SQ
Sponsors
Eli Lilly and Company
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
12 Years to 17 Years
Healthy volunteers
No
Inclusion criteria
* Have a diagnosis of chronic migraine as defined by the IHS ICHD-3 guidelines (1.3 according to ICHD-3 \[2018\]), that is, a headache occurring on 15 or more days per month for at least the last 3 months, which has the features of migraine headache on at least 8 days per month.
Exclusion criteria
* Participants who are taking, or are expected to take, therapeutic antibodies during the course of the study (adalimumab, infliximab, trastuzumab, bevacizumab, etc.). Prior use of therapeutic antibodies is allowed if that use was more than 12 months prior to baseline, except for antibodies to CGRP or its receptor, which are not allowed at any time prior to study entry. * Known hypersensitivity monoclonal antibodies or other therapeutic proteins, or to galcanezumab or its excipients. * Current use or prior exposure to galcanezumab, another CGRP antibody, or CGRP receptor antibody, including those who have previously completed or withdrawn from this study or any other study investigating a CGRP antibody. Participant must also not have prior oral CGRP antagonist use within 30 days prior to baseline. * History of IHS ICHD-3 diagnosis of new daily persistent headache, cluster headache or migraine subtypes including hemiplegic (sporadic or familial) migraine and migraine with brainstem aura (previously basilar-type migraine). * History of significant head or neck injury within 6 months prior to screening; or traumatic head injury at any time that is associated with significant change in the quality or frequency of their headaches, including new onset of migraine following traumatic head injury. * Participants with a known history of intracranial tumors or developmental malformations including Chiari malformations.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change from Baseline in the Number of Monthly Migraine Headache Days | Baseline, 3 Months | Change from Baseline in the Number of Monthly Migraine Headache Days |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of Participants with Reduction from Baseline ≥30%, ≥50%, ≥75% and 100% in Monthly Migraine Headache Days | 3 Months | Percentage of Participants with Reduction from Baseline ≥30%, ≥50%, ≥75% and 100% in Monthly Migraine Headache Days |
| Change from Baseline in the Number of Monthly Migraine Headache Days with Nausea and/or Vomiting | Baseline, 3 Months | Change from Baseline in the Number of Monthly Migraine Headache Days with Nausea and/or Vomiting |
| Change from Baseline in the Number of Monthly Migraine Headache Days with Photophobia and Phonophobia | Baseline, 3 Months | Change from Baseline in the Number of Monthly Migraine Headache Days with Photophobia and Phonophobia |
| Change from Baseline in the Number of Monthly Migraine Headaches with Prodromal Symptoms | Baseline, 3 Months | Change from Baseline in the Number of Monthly Migraine Headaches with Prodromal Symptoms |
| Change from Baseline in the Number of Monthly Migraine Headache Days on Which Acute Headache Medication is Taken | Baseline, 3 Months | Change from Baseline in the Number of Monthly Migraine Headache Days on Which Acute Headache Medication is Taken |
| Patient Global Impression-Improvement (PGI-I) Rating | Month 1 to Month 3 | PGI-I Rating |
| Change from Baseline in the Severity of Remaining Migraine Headaches per Month | Baseline, 3 Months | Change from Baseline in the Severity of Remaining Migraine Headaches per Month |
| Change from Baseline in the Number of Monthly Headache Days | Baseline, 3 Months | Change from Baseline in the Number of Monthly Headache Days |
| Change from Baseline on the Pediatric Quality of Life Inventory (PedsQL) Total Score | Baseline, 3 Months | Change from Baseline on the PedsQL Total Score |
| Change from Baseline on the Pediatric Migraine Disability Assessment test (PedMIDAS) Total Score | Baseline, 3 Months | Change from Baseline on the PedMIDAS Total Score |
| Percentage of Participants with Suicidal Ideation and Behaviors Assessed by the Columbia Suicide Severity Rating Scale (C-SSRS) Score | Baseline through 3 Months | Percentage of Participants with Suicidal Ideation and Behaviors Assessed by the C-SSRS Score |
| Pharmacokinetics (PK): Serum Concentration of Galcanezumab | Baseline through 3 Months | PK: Serum Concentration of Galcanezumab |
| Plasma Concentration of Calcitonin Gene-Related Peptide (CGRP) | Baseline through 3 Months | Plasma Concentration of CGRP |
| Percentage of Participants Developing Anti-Drug Antibodies | Baseline through 3 Months | Percentage of Participants Developing Anti-Drug Antibodies |
| Percentage of Participants who Initiate Migraine Prevention Medication in the Post-Treatment Follow-Up Phase | 16 Months | Percentage of Participants who Initiate Migraine Prevention Medication in the Post-Treatment Follow-Up Phase |
Countries
Denmark, France, Germany, India, Italy, Japan, Mexico, Netherlands, Puerto Rico, Spain, United States
Contacts
STUDY_DIRECTORCall 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 8 AM - 8 PM Eastern time (UTC/GMT - 5 hours, EST)
Eli Lilly and Company
Outcome results
None listed