Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 2:23 PM
Ignite Modification Date:
2025-12-25 @ 12:59 PM
NCT ID:
NCT01446159
Group ID:
EG002
Title:
MEDI-573 45 mg/kg + AI
Description:
Participants received intravenous infusion of MEDI-573 45 mg/kg on Day 1 of each 21-day cycle and AI (letrozole, anastrozole, or exemestane) orally once daily until unacceptable toxicity, documentation of disease progression, or withdrawal for other reasons. Three participants were enrolled in Phase 1b and 89 were enrolled in Phase 2 of the study.
Deaths Number Affected:
43
Deaths Number At Risk:
None
Serious Number Affected:
21
Serious Number At Risk:
92
Other Number Affected:
86
Other Number At Risk:
92
Study:
NCT01446159
Results Section:
NCT01446159
Adverse Events Module:
NCT01446159