drugset / Trial / NCT01613248
A Dose-Finding Study of MK-1602 in the Treatment of Acute Migraine (MK-1602-006)
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
Publications
- Background Voss T, Lipton RB, Dodick DW, Dupre N, Ge JY, Bachman R, Assaid C, Aurora SK, Michelson D. A phase IIb randomized, double-blind, placebo-controlled trial of ubrogepant for the acute treatment of migraine. Cephalalgia. 2016 Aug;36(9):887-98. doi: 10.1177/0333102416653233. Epub 2016 Jun 6.
- Goadsby PJ, Jurgens TP, Brand-Schieber E, Nagy K, Liu Y, Boinpally R, Stodtmann S, Trugman JM. Efficacy of ubrogepant and atogepant in males and females with migraine: A secondary analysis of randomized clinical trials. Cephalalgia. 2025 Feb;45(2):3331024251320610. doi: 10.1177/03331024251320610.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |