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:
2025-12-25 @ 12:03 AM
Ignite Modification Date:
2025-12-25 @ 10:02 PM
NCT ID:
NCT02178358
Group ID:
EG001
Title:
150 mg Galunisertib + 400 mg Sorafenib Therapy
Description:
150 mg galunisertib administered orally, BID for 14 days followed by 14 days with no study drug (28 days cycle).
400 mg sorafenib administered orally BID for 28 days.
Deaths Number Affected:
58
Deaths Number At Risk:
None
Serious Number Affected:
31
Serious Number At Risk:
74
Other Number Affected:
73
Other Number At Risk:
74
Study:
NCT02178358
Results Section:
NCT02178358
Adverse Events Module:
NCT02178358