drugset / Trial / NCT00701389

Study to Evaluate the Safety, Tolerability, and Blood Pressure Effect of an Oral Dose of Sumatriptan Alone and in Combination With MK-0974 (Telcagepant) in Migraine Patients (0974-026)

NCT00701389

Phase 1 Completed 24 enrolled Merck Sharp & Dohme LLC
RandomizedCrossoverDouble-blindTreatment

Summary

Study to understand the effects of migraine treatments on blood pressure in participants with migraine. The primary hypothesis is that the effect on semi-recumbent mean arterial pressure following the coadministration of telcagepant and sumatriptan is similar to that following administration of sumatriptan alone. That is, the true mean treatment difference (sumatriptan with telcagepant sumatriptan alone) in time-weighted mean arterial pressure for 2.5 hours following dosing is less than 5 mmHg.

Timeline

Start
2007-11-20
Primary completion
2008-04-10
Completion
2008-04-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Sumatriptan Unknown 100 mg Oral
Subject Telcagepant Small molecule 600 mg Oral

Indications