Study Condition(s): Episodic Cluster Headache

A Study of LY2951742 in Participants With Episodic Cluster Headache

Study Alias: CGAL

Study Identifier(s): Tool Tip Icon {{ defaultRegistry.registryAnchorText }} NCT02397473 {{ currentLocaleObject.registryAnchorText }}

Recruiting Recruiting

Study Purpose

The main purpose of this study is to evaluate the efficacy and safety of the study drug known as LY2951742 in participants with episodic cluster headaches.

Key Participation Requirements Tool Tip Icon

All clinical trials have rules about who can participate. This section outlines some of those rules. Please contact a study center to discuss the full set of criteria

Gender

Male Female

Age

18 years
65 years

Time Commitment

Your participation will include scheduled office visits throughout the study period
  • Participant must present with a history of episodic cluster headache (investigator to provide more details)

  • Participant must be able to distinguish cluster headache attacks from other headaches

  • Participant must not be taking indomethacin

  • Female participant must not be pregnant or nursing

Where to Participate

53 locations are currently available of 53 planned
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