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 @ 4:55 PM
Ignite Modification Date:
2025-12-25 @ 2:37 PM
NCT ID:
NCT01229150
Group ID:
EG000
Title:
KRAS Mut 2 & WT KRAS 2
Description:
KRAS Mutant patients randomized to combination therapy arm
AZD6244 + Erlotinib: For KRAS mutant patients and Wild-Type KRAS 2 patients randomized to the combination arm (arms are stratified based on KRAS mutational status), AZD6244 150 mg qd (every day) + erlotinib mg qd.
Deaths Number Affected:
17
Deaths Number At Risk:
None
Serious Number Affected:
30
Serious Number At Risk:
49
Other Number Affected:
49
Other Number At Risk:
49
Study:
NCT01229150
Results Section:
NCT01229150
Adverse Events Module:
NCT01229150