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Effectiveness and Tolerability of Zavegepant for Acute Migraine Treatment Among Those Using CGRP Targeting Preventive Medications - Trial NCT06401642

Access comprehensive clinical trial information for NCT06401642 through Pure Global AI's free database. This Phase 4 trial is sponsored by Mayo Clinic and is currently Not yet recruiting. The study focuses on Migraine. Target enrollment is 200 participants.

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NCT06401642
Phase 4
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06401642
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Effectiveness and Tolerability of Zavegepant for Acute Migraine Treatment Among Those Using CGRP Targeting Preventive Medications
A Study to Assess Effectiveness and Tolerability of Zavegepant as an Acute Migraine Treatment Among Those Using CGRP Targeting Preventive Medications.

Study Focus

Migraine

Zavegepant

Interventional

drug

Sponsor & Location

Mayo Clinic

Scottsdale, United States of America

Timeline & Enrollment

Phase 4

May 01, 2024

Mar 01, 2027

200 participants

Primary Outcome

Headache relief in 2 hours,Headache relief in 4 hours,Functional disability level in 2 hours,Functional disability level in 4 hours

Summary

Zavegepant (Zavzpret) is approved for the acute treatment of migraine with or without aura in
 the US. The purpose of this study is to investigate the effectiveness and tolerability of
 zavegepant for the acute treatment of migraine attacks amongst participants who are using
 calcitonin gene-related peptide (CGRP) migraine preventive treatments.

ICD-10 Classifications

Migraine
Other migraine
Migraine, unspecified
Complicated migraine
Headache

Data Source

ClinicalTrials.gov

NCT06401642

Non-Device Trial