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 @ 4:02 PM
Ignite Modification Date:
2025-12-25 @ 2:04 PM
NCT ID:
NCT04478266
Group ID:
EG001
Title:
Amcenestrant + Palbociclib
Description:
Participants received amcenestrant 200 mg tablet along with letrozole-matching placebo once daily, continuously and palbociclib 125 mg PO, QD from Day 1 to Day 21 of each 28-day treatment cycle until disease progression, death or study cut-off date, whichever comes first (maximum exposure: 109 weeks).
Deaths Number Affected:
45
Deaths Number At Risk:
None
Serious Number Affected:
77
Serious Number At Risk:
533
Other Number Affected:
412
Other Number At Risk:
533
Study:
NCT04478266
Results Section:
NCT04478266
Adverse Events Module:
NCT04478266