Studies how the migraine drug eptinezumab works in the body
Tests eptinezumab, a migraine treatment, in adults who have migraine.
Key facts
- Who runs it
- Ospedale San Raffaele S.r.l.
- Where
- Milan, ItalySee the site
- Trial code
- Registry title
- Exploring Eptinezumab: Unveiling Peripheral and Central Mechanisms of Action and Searching for Biomarkers of Patient Response (EUPHORIA Study)
- Status
- Recruiting
- Phase
- Phase 4
- People taking part
- 60 people, planned
- Started
- 8 Jan 2026
- Expected to end
- 15 Nov 2027
- Type of study
- Interventional
- Record updated
- 10 February 2026
Who can take part
AI summary
From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.
The trial is looking for adults with migraine who have not responded to several preventive treatments and can start eptinezumab 100mg. Healthy adults can also join as a comparison group.
- Age
- 18 years or older
- Sex
- All
- Disease stage
- Migraine with or without aura for at least 12 months, with 8 or more migraine days per month on average over the last three months. Migraine-related disability must be moderate or severe (MIDAS questionnaire). Healthy controls have no headaches except rare tension-type headache.
- Earlier treatment
- Three or more earlier preventive treatments (such as tricyclics, anticonvulsants, beta-blockers, onabotulinum toxin A) did not work or were not tolerated. Must be able to receive eptinezumab under Italian Health System reimbursement rules.
Main reasons for not taking part
- Currently using other preventive or acute treatment that targets the CGRP pathway
- History of medication overuse headache
- Heart or brain blood vessel disease, such as heart attack, stroke, or unstable angina
- Other chronic headache or chronic pain conditions
- Pregnancy or breastfeeding, or a condition that makes an MRI scan unsafe
The registry criteria, word for word
Show all 37 criteriaShow less
Who can take part
- Individuals aged ≥ 18 years
- Healthy controls aged ≥ 18 years
- Healthy controls right-handedness
- Healthy controls able to autonomously sign the informed consent prior to study enrolment
- Right-handedness
- Able to autonomously sign the informed consent prior to study enrolment
- History of migraine with or without aura for at least 12 months prior to study enrolment, based on the diagnostic criteria of the International Classification of Headache Disorders version 3rd edition (ICHD-3)1, as determined from medical records and/or migraine participants self-report
- Eligibility for treatment with eptinezumab according to the current reimbursement policies of the Italian Health System
- Migraine frequency of ≥8 migraine days per month on average across the three months prior to study enrolment
- Failure to respond to three or more previous preventive treatments, including tricyclics, anticonvulsants, beta-blockers, and onabotulinum toxin A, due to either lack of efficacy or poor tolerability. Efficacy failure is defined as no reduction in headache and migraine frequency, duration, or severity after administering the respective medication for at least 6 weeks at approved therapeutic dose(s). Tolerability failure is defined as documented discontinuation due to adverse events of the respective medication at any time prior to screening
- Migraine-related disability as moderate or severe according to the Migraine Disability Assessment (MIDAS) questionnaire
- Female subjects of childbearing potential must practice at least one of the following specified method of birth control during the study: combined (estrogen and progestogen containing) hormonal birth control (oral, intravaginal, transdermal, injectable); progestogen-only hormonal birth control (oral, injectable, implantable); bilateral tubal occlusion/ligation; intrauterine device; intrauterine hormone-releasing system; vasectomized partner; practice true abstinence, a barrier method (male condom or female condom) with or without spermicide or cap, diaphragm or sponge with spermicide
Who cannot take part
- Currently receiving more than one other prophylactic treatment for migraine
- Currently using other preventive treatment targeting the CGRP pathway
- Currently using acute treatments targeting the CGRP pathway
- Evidence of drug or alcohol abuse or dependence within 12 months prior to study enrolment in healthy controls
- Evidence of drug or alcohol abuse or dependence within 12 months prior to study enrolment
- History of medication overuse headache according to the ICHD-3 criteria1
- History of any headaches except for infrequent tension-type headache for healthy controls
- Cardio or cerebrovascular comorbidities, such as myocardial infarction, stroke, transient ischemic attack, unstable angina in healthy controls
- Cardio or cerebrovascular comorbidities, such as myocardial infarction, stroke, transient ischemic attack, unstable angina
- Poor controlled blood hypertension in healthy controls
- Other chronic pain disorders and neuropathic pain in healthy controls
- History of head trauma or seizure or major psychiatric disorders or suicidal ideation/behaviour in healthy controls
- Clinical conditions contraindicating a MRI scan, such as pacemakers, aneurysm clips, artificial heart valves, ear implants, foreign metal objects in the eyes, skin, or body, or any other condition deemed hazardous in combination with MRI, in healthy controls
- Poor controlled blood hypertension
- Other chronic headache conditions, such as cluster headache, hemiplegic migraine headache or persistent post-traumatic headache
- Other chronic pain disorders and neuropathic pain
- History of head trauma or seizure or major psychiatric disorders or suicidal ideation/behaviour
- Clinical conditions contraindicating a MRI scan, such as pacemakers, aneurysm clips, artificial heart valves, ear implants, foreign metal objects in the eyes, skin, or body, or any other condition deemed hazardous in combination with MRI
- Age older than 50 years at migraine onset
- Needle phobia
- Unable to differentiate migraine from other headaches
- Use of one migraine preventive treatment without a stable dosage for the last two months
- Needle phobia for healthy controls
- For females healthy controls, pregnancy or breastfeeding
- For females, pregnancy or breastfeeding
Where in Italy
- Ospedale San Raffaele S.r.l.Milan, ItalyTaking people
About the trial
What the trial wants to find out
1. To identify reference values specific to migraine for measures of central and peripheral sensitization. 2. To identify treatment-induced changes in measures of central and/or peripheral sensitization, from baseline to week 12 of eptinezumab 100mg, and to explore correlation between treatment-induced changes in candidate measures of sensitization and clinical efficacy measures at 12 weeks of treatment with eptinezumab 100mg (analysis: changes intra patients treated with eptinezumab 100mg).
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Contact the study team: see the registry record
Print a page for my doctorData and sources
- Registry record
- Listed on the EU's official list of trials (CTIS).
- Official title
- Exploring Eptinezumab: Unveiling Peripheral and Central Mechanisms of Action and Searching for Biomarkers of Patient Response (EUPHORIA Study)
- Plain-language title
- Studies how the migraine drug eptinezumab works in the bodyGenerated from the registry record. The registry title is the official one.
- AI summary
- From the trial's eligibility criteria. Read by machine on 9 November 2026.
- Record updated
- 10 February 2026