Study of Telcagepant (MK-0974) in Participants With Moderate to Severe Acute Migraine With or Without Aura (MK-0974-011)

PHASE3CompletedINTERVENTIONAL
Enrollment

1,380

Participants

Timeline

Start Date

February 15, 2007

Primary Completion Date

October 2, 2007

Study Completion Date

October 2, 2007

Conditions
Migraine
Interventions
DRUG

Telcagepant potassium 150 mg

Telcagepant 150 mg liquid-filled soft gel capsules

DRUG

Telcagepant potassium 300 mg

Telcagepant 300 mg liquid-filled soft gel capsules

DRUG

Zolmitriptan 5 mg

Zolmitriptan 5 mg tablets

DRUG

Placebo to telcagepant 150 mg

Placebo to match telcagepant 150 mg liquid-filled soft gel capsules

DRUG

Placebo to tecagepant 300 mg

Placebo to match tecagepant 300 mg liquid-filled soft gel capsules

DRUG

Placebo to zolmitriptan 5 mg

Placebo to match zolmitriptan 5 mg tablets

DRUG

Rescue medication

If moderate or severe migraine headache pain continues or recurs 2 hours after dose of study drug, participants are allowed to take an optional second dose of study drug or their own non-study rescue migraine medication, which may include analgesics (e.g., nonsteroidal anti-inflammatory drugs \[NSAIDs\] or opiates), anti-emetics, or zolmitriptan. Triptans other than zolmitriptan and ergot derivatives are prohibited for 24 hours following the last dose of study drug.

All Listed Sponsors
lead

Merck Sharp & Dohme LLC

INDUSTRY

NCT00442936 - Study of Telcagepant (MK-0974) in Participants With Moderate to Severe Acute Migraine With or Without Aura (MK-0974-011) | Biotech Hunter | Biotech Hunter