MK0462 5 mg, Sumatriptan 50 mg, and Placebo Comparison Study (0462-029)

• Status: Completed
• Trial end date: 1996-09-01
• Target enrollment: 0
• Participant gender: All

Summary

A study to compare rizatriptan (MK0462) 5 mg by mouth (p.o.) and sumatriptan 50 mg p.o. for the acute treatment of a migraine attack.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Merck Sharp & Dohme Corp.
• Treatments: Rizatriptan; Sumatriptan

Criteria

Inclusion Criteria:

• Participant had at least a 6-month history of migraine, with or without aura

• Participant was male, or if female, must have been postmenopausal, surgically sterilized, or taking adequate contraceptive precautions

• Participant was judged to be in good health, apart from migraine

Exclusion Criteria:

• Participant was Pregnant or a nursing mother

• Participant had a history or current evidence of drug or alcohol abuse

• Participant had a history or clinical evidence of cardiovascular disease

• Participant had a clinically significant Electrocardiography (ECG) abnormality

• Participant had a resting systolic blood pressure of greater than 145 mm Hg or diastolic of less than 95 mm Hg at screening

• Participant had received treatment with an investigational device or compound within 30 days of the study

• Participant typically suffered from less then 1 or more than 8 attacks of migraine per month

• Participant had difficulty in distinguishing his/her migraine attacks from tension or interval headaches

• Participant was currently taking monoamine oxidase inhibitors, methysergide or lithium