Open Label Safety Study in Acute Treatment of Migraine

NCT03266588 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 3019

Last updated 2023-02-16

Study results available
· View outcomes & findings →

Summary

The purpose of this study is to evaluate safety and tolerability of BHV-3000 (rimegepant).

Conditions

  • Migraine, With or Without Aura

Interventions

DRUG

Rimegepant

75 mg oral tablet

Sponsors & Collaborators

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-08-30
Primary Completion
2019-07-15
Completion
2019-07-15
FDA Drug
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03266588 on ClinicalTrials.gov