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NCT05888766

Predict the Response to Acute Treatment of Migraine With Rimegepant 75 mg

Status unknown Last updated 5 June 2023
What this trial tests

trial testing Rimegepant 75 milligrams in Migraine Disorders in 20 participants. Status unknown.

Timeline
1 July 2023
Primary endpoint
30 July 2024
30 September 2024

Quick facts

Lead sponsorUniversity of Roma La Sapienza
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment20
Start date1 July 2023
Primary completion30 July 2024
Estimated completion30 September 2024
Sites1 location across Italy

Drugs / interventions tested

Conditions studied

Sponsor

University of Roma La Sapienza

Who can join

Adults 18 to 65, any sex, with Migraine Disorders. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Tools to predict which patients could better respond to abortive CGRP target therapy are still lacking. We propose to investigate if biochemical (salivary CGRP) and neurophysiological (evoked potentials) biomarkers can recognize patients with the best chances of responding to Rimegepant 75 mg as an acute treatment of migraine.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Migraine Disorders

Currently open trials in the same condition.

Other University of Roma La Sapienza trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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