The main purpose of this study is to evaulate the efficacy and safety of galcanezumab in participants 6 to 17 years of age for the preventive treatment of episodic migraine. The primary objective is to demonstrate the superiority of galcanezumab versus placebo in the reduction of monthly migraine headache days across the 3-month double-blind treatment period.
The study has two parts which enroll separately from each other such that participants may choose to participate in either but not both: the main study and a study addendum.
|Clinical Study Identifier||NCT03432286|
|Sponsor||Eli Lilly and Company|
|Last Modified on||14 January 2021|
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