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 @ 12:01 AM
Ignite Modification Date:
2025-12-25 @ 9:59 PM
NCT ID:
NCT01306058
Group ID:
EG000
Title:
Sorafenib & TRC105 in Hepatocellular CA
Description:
CA (cancer); 15 mg/kg TRC105 intravenous (IV) every 2 weeks and 400 mg sorafenib by mouth (PO) twice per day
TRC 105: 15 mg/kg IV every 2 weeks
Sorafenib: 400 mg twice a day (bid) continuously in a 28 days cycle
Deaths Number Affected:
16
Deaths Number At Risk:
None
Serious Number Affected:
11
Serious Number At Risk:
27
Other Number Affected:
27
Other Number At Risk:
27
Study:
NCT01306058
Results Section:
NCT01306058
Adverse Events Module:
NCT01306058