Selective Activation of the Adrenomedullin Receptors in Migraine
Recruiting · NCT07451769 · Interventional (participants receive a specific treatment) · Lead sponsor: Danish Headache Center
View the official record on ClinicalTrials.gov →Interventions studied
AdrenomedullinPlacebo
What this trial is about
Adrenomedullin is a neuropeptide implicated in the pathogenesis of migraine. This study investigates whether its administration, after pre-treatment with erenumab (a CGRP-receptor blocking monoclonal antibody), can trigger migraine attacks in individuals with migraine without aura.
Who can take part
Age range
18 Years to 65 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not applicable (e.g. observational or device study)
Study type
Interventional (participants receive a specific treatment)
Inclusion criteria
- Written informed consent has been obtained prior to the initiation of any study-specific procedures.
- Age ≥18 years at the time of screening.
- History of migraine without aura for at least 12 months prior to screening, with a frequency of 1-5 migraine attacks per month, based on medical records and/or patient self-report, and diagnosed in accordance with the ICHD-3 criteria.
Exclusion criteria
- History of any other primary headache disorder, except for tension-type headache with \<5 headache days per month, based on ICHD-3 classification.
- History of any secondary headache disorder, per ICHD-3 criteria, prior to screening.
- Use of prophylactic migraine medication within 30 days or within 5 plasma half-lives (whichever is longer) prior to screening.
- Previous use of any therapies targeting the CGRP signaling pathway, including anti-CGRP ligand monoclonal antibodies, anti-CGRP receptor monoclonal antibodies, or small molecule CGRP receptor antagonists.
- Known risk of self-harm or harm to others, including a history of suicidal behavior.
- Any clinically significant disorder, condition, or disease (other than those permitted in the protocol) that, in the opinion of the investigator, could compromise participant safety or interfere with study procedures or data integrity.
- Positive urine pregnancy test at screening or on Day 1 in female participants of childbearing potential.
- Pregnancy or breastfeeding, or plans to become pregnant or breastfeed during the study period.
- Evidence of current pregnancy or breastfeeding based on self-report or medical records.
- Inability or unwillingness to complete all protocol-required visits and procedures, or concerns regarding protocol adherence, as judged by the investigator.
Where it is running
1 location listed.
- Danish Headache Center - Glostrup Municipality, Denmark