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 @ 7:36 PM
Ignite Modification Date:
2025-12-25 @ 5:17 PM
NCT ID:
NCT02107703
Group ID:
EG001
Title:
Placebo + Fulvestrant
Description:
Placebo administered orally every 12 hours on Days 1 to 28 of a 28-day cycle in combination with fulvestrant 500mg administered IM on Days 1 and 15 of Cycle 1, then on Day 1 of Cycle 2 and beyond. Participants received treatment until discontinuation were met.
Deaths Number Affected:
157
Deaths Number At Risk:
None
Serious Number Affected:
33
Serious Number At Risk:
223
Other Number Affected:
194
Other Number At Risk:
223
Study:
NCT02107703
Results Section:
NCT02107703
Adverse Events Module:
NCT02107703