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 @ 5:03 PM
Ignite Modification Date:
2025-12-25 @ 2:43 PM
NCT ID:
NCT00308750
Group ID:
EG000
Title:
Enzastaurin/Pemetrexed/Carboplatin
Description:
Enzastaurin loading dose of 1125 mg or 1200 mg on Day -7 (pre-chemotherapy) followed by 500 mg administered once daily starting from Day -6 until disease progression.
Pemetrexed 500 mg/m\^2 and carboplatin AUC 6 mg\*min/mL as an intravenous infusion on Day 1 every 21 days for a maximum of 6 cycles (21-day cycle) or disease progression whichever came first.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
35
Serious Number At Risk:
67
Other Number Affected:
63
Other Number At Risk:
67
Study:
NCT00308750
Results Section:
NCT00308750
Adverse Events Module:
NCT00308750