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NCT06409832: RAISE

RimegepAnt effectIvenesS and tolErability as Migraine Preventive Treatment: a Prospective, Multicentric, Cohort Study (RAISE)

Recruiting now Last updated 19 January 2026
What this trial tests

trial testing Rimegepant 75 mg in Migraine in 100 participants. Currently enrolling.

Timeline
26 March 2024
Primary endpoint
1 January 2027
1 September 2027

Quick facts

Lead sponsorUniversity of Florence
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment100
Start date26 March 2024
Primary completion1 January 2027
Estimated completion1 September 2027
Sites2 locations across Italy

Drugs / interventions tested

Conditions studied

Sponsor

University of Florence

Who can join

18 and older, any sex, with Migraine or Migraine With Aura. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this prospective and multicentric study is to evaluate the effectiveness and tolerability of rimegepant as preventive migraine treatment in a cohort of episodic or chronic migraine patients.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Migraine

Currently open trials in the same condition.

Other University of Florence trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06409832.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing