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 @ 2:39 PM
Ignite Modification Date:
2025-12-25 @ 1:11 PM
NCT ID:
NCT00125359
Group ID:
EG000
Title:
Single Arm Erlotinib + Bexarotene
Description:
All eligible patients will receive continuous daily oral erlotinib 150mg with daily bexarotene oral capsules 400mg.
erlotinib and bexarotene: Daily Erlotinib 150mg and daily bexarotene oral capsules 400mg.
Deaths Number Affected:
4
Deaths Number At Risk:
None
Serious Number Affected:
30
Serious Number At Risk:
42
Other Number Affected:
14
Other Number At Risk:
42
Study:
NCT00125359
Results Section:
NCT00125359
Adverse Events Module:
NCT00125359