Viewing Study NCT07159750


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Ignite Modification Date: 2026-01-01 @ 7:17 AM
Study NCT ID: NCT07159750
Status: RECRUITING
Last Update Posted: 2025-09-08
First Post: 2025-08-23
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Real-world Prospective Study on the Use of Anti-CGRP Drugs in Migraine
Sponsor: Hospital Universitari Vall d'Hebron Research Institute
Organization:

Study Overview

Official Title: Real-world Prospective Study on the Use of Anti-CGRP Drugs in Migraine
Status: RECRUITING
Status Verified Date: 2025-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: EUREkA
Brief Summary: The goal of this observational study is to evaluate clinical differences in patients who received preventive treatment with medication targeting calcitonin gene-related peptide (CGRP) or its receptor: monoclonal antibodies (erenumab, galcanezumab, fremanezumab, eptinezumab) or gepants (rimegepant, atogepant) during a 2-year period observation phase.
Detailed Description: It is a 2-year, multicenter observational study. Patients who meet reimbursement criteria according to local regulations and willing to participate in the study will be included. Monoclonal antibodies (erenumab, galcanezumab, fremanezumab, eptinezumab) or gepants (rimegepant, atogepant) will be started and baseline assessment will be conducted. There will be visits every 6 months to assess effectiveness, side-effects, PROMs, and elegibility to continue with the study drug. The observation of patients will last 2 years.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: