A Study of LY2951742 in Participants With Migraine

Status Completed

Clinical Trial Summary

To assess the efficacy and safety of LY2951742 in the prevention of migraine headache in migraineurs with or without aura during 3 months of treatment.

Clinical Trial Description

The study is comprised of 4 trial periods:

1. Screening and washout (5-45 days)

2. Baseline for assessment of the type, frequency, and severity of headaches (28-38 days)

3. Treatment (12 weeks)

4. Follow-up (12 weeks) ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01625988
Study type	Interventional
Source	Eli Lilly and Company
Contact
Status	Completed
Phase	Phase 2
Start date	June 28, 2012
Completion date	September 18, 2013

View Details

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