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 @ 11:08 PM
Ignite Modification Date:
2025-12-25 @ 8:40 PM
NCT ID:
NCT02505269
Group ID:
EG000
Title:
Brentuximab Vedotin
Description:
The following procedures will take place during study visits beginning after the screening procedures:
\- Participants will receive combination therapy:
* Brentuximab Vedotin intravenously on predetermined days per cycle
* Adriamycin intravenously on predetermined days per cycle
* Dacarbazine intravenously on predetermined days per cycle
Brentuximab Vedotin
Adriamycin
Dacarbazine
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
5
Serious Number At Risk:
34
Other Number Affected:
34
Other Number At Risk:
34
Study:
NCT02505269
Results Section:
NCT02505269
Adverse Events Module:
NCT02505269