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 @ 10:04 PM
Ignite Modification Date:
2025-12-25 @ 7:40 PM
NCT ID:
NCT03126435
Group ID:
EG000
Title:
EndoTAG-1 and Gemcitabine
Description:
EndoTAG-1 22 mg/m² twice weekly plus Gemcitabine 1000 mg/m² once weekly for 1 cycle (8 weeks) consisting of 3 weeks of treatment and 1 week rest followed by 3 weeks of treatment and 1 week rest until any one of the following occurs: progressive disease or unacceptable toxicity or withdrawal of consent.
EndoTAG-1: twice weekly
Gemcitabine: once weekly
Deaths Number Affected:
91
Deaths Number At Risk:
None
Serious Number Affected:
52
Serious Number At Risk:
102
Other Number Affected:
101
Other Number At Risk:
102
Study:
NCT03126435
Results Section:
NCT03126435
Adverse Events Module:
NCT03126435