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Eptinezumab as Preventive Treatment of Migraine in Adults With Migraine

Sponsored by H. Lundbeck A/S

About this trial

Last updated 10 months ago

Study ID

19140A

Status

Active, not recruiting

Type

Interventional

Phase

Phase 3

Placebo

Yes

Accepting

18-75 Years
18 to 75 Years
All
All

Not accepting

Not accepting
Healthy Volunteers

Trial Timing

Ended 3 months ago

What is this trial about?

This study evaluates the efficacy of eptinezumab to prevent migraine in participants with chronic migraine.

What are the participation requirements?

Yes

Inclusion Criteria

- The participant has a diagnosis of CM as defined by IHS ICHD-3 guidelines confirmed at screening visit with a history of migraine onset at least 12 months prior to the Screening Visit. - The participant has a migraine onset at ≤50 years of age. - The participant has ≥8 migraine days per month for each month within the past 3 months prior to the Screening Visit. - The participant fulfils the following criteria for migraine in prospectively collected information in the eDiary during the screening period: - Migraine occurring on ≥8 days and headache occurring on ≥15 to ≤26 days. - The participant has demonstrated compliance with the Headache eDiary by entry of data for at least 24 of the 28 days following the Screening Visit. - The participant is aged ≥18 (≥20 for Taiwan) and ≤75 years at the Screening Visit.

No

Exclusion Criteria

- The participant has received any medication targeting the calcitonin gene-related peptide (CGRP) pathway as preventive treatment of migraine. - The participant has confounding and clinically significant pain syndromes, (for example, fibromyalgia, chronic low back pain, complex regional pain syndrome). - The participant has a diagnosis of acute or active temporomandibular disorder. - The participant has a history or diagnosis of 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), ophthalmoplegic migraine, migraine with brainstem aura and migraine with neurological accompaniments that are not typical of migraine aura (diplopia, altered consciousness, or long duration). - The participant has a lifetime history of psychosis, bipolar mania, or dementia. - Participants with other psychiatric conditions whose symptoms are not controlled or who have not been adequately treated for a minimum of 6 months prior to screening are also excluded. - The participant has a history of clinically significant cardiovascular disease, including uncontrolled hypertension, vascular ischaemia or thromboembolic events (for example, cerebrovascular accident, deep vein thrombosis, or pulmonary embolism). Other inclusion and exclusion criteria may apply