Chronic Migraine, Episodic Migraine
Conditions
Keywords
Episodic migraine, Chronic migraine
Brief summary
This study will evaluate the Long-Term Safety and Tolerability of Atogepant 60 mg daily for the Prevention of Migraine in Participants with Chronic or Episodic Migraine
Interventions
DRUGAtogepant 60 mg
Tablets containing 60 mg of Atogepant
Sponsors
AbbVie
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
\- Eligible participants who completed Visit 7, and Visit 8 if applicable, of Study 3101-303-002 or Study 3101-304-002 without significant protocol deviations and who did not experience an Adverse Event that may indicate an unacceptable safety risk.
Exclusion criteria
* Participants requiring any medication, diet, or nonpharmacological treatment on the list of prohibited concomitant medications or treatments that cannot be discontinued or switched to an allowable alternative. * Participants with an ECG indicating clinically significant abnormalities at Visit 1. * Participants with hypertension at Visit 1. * Participants with a significant risk of self-harm, or of harm to others; participants who report suicidal ideation with intent, with or without a plan, since the last visit, must be excluded. * Participants with clinically significant hematologic, endocrine, cardiovascular, pulmonary, renal, hepatic, gastrointestinal, or neurologic disease.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Percentage of Participants with at Least 1 Treatment Emergent Adverse Event | 156 weeks |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Percentage of Participants with Clinically Significant Laboratory Values (Chemistry, Hematology, Urinalysis) as assessed by the Investigator | 156 weeks | — |
| Percentage of Participants with Clinically Significant Electrocardiograms (ECGs) Findings as assessed by the Investigator | 156 weeks | — |
| Percentage of Participants with Clinically Significant Vital Sign Measurements as assessed by the Investigator | 156 weeks | — |
| Columbia-Suicide Severity Rating Scale (C-SSRS) Assessing Suicidal Ideation and Behaviour using 5-Point Scales | 156 weeks | A clinician-rated instrument that reports the severity of both suicidal ideation and behavior. Suicidal ideation is classified on a 5-item scale: 1 (wish to be dead), 2 (nonspecific active suicidal thoughts), 3 (active suicidal ideation with any methods \[not plan\] without intent to act), 4 (active suicidal ideation with some intent to act, without specific plan), and 5 (active suicidal ideation with specific plan and intent). Suicidal behavior is classified on a 5-item scale: 0 (no suicidal behavior), 1 (preparatory acts or behavior), 2 (aborted attempt), 3 (interrupted attempt), and 4 (actual attempt). More than 1 classification can be selected provided they represent separate episodes. (Minimum total score 0, maximum total score 5; higher total scores indicate more suicidal ideation and/or suicidal behavior) |
Countries
Canada, Czechia, Denmark, France, Germany, Hungary, Italy, Netherlands, Poland, South Korea, Spain, Taiwan, United Kingdom, United States
Outcome results
None listed