drugset / Trial / NCT01613248

A Dose-Finding Study of MK-1602 in the Treatment of Acute Migraine (MK-1602-006)

NCT01613248 ↗

Phase 2 Completed 834 enrolled Allergan
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the effectiveness, safety and tolerability of a range of doses of MK-1602 versus placebo in the treatment of acute migraine.

Timeline

Start
2012-07-01
Primary completion
2012-12-01
Completion
2012-12-01

Drugs

EvaluationDrugModalityDoseRoute
Subject MK-1602 Unknown 1 mg Oral
Subject MK-1602 Unknown 10 mg Oral
Subject MK-1602 Unknown 25 mg Oral
Subject MK-1602 Unknown 50 mg Oral
Subject MK-1602 Unknown 100 mg Oral

Indications