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 @ 4:53 PM
Ignite Modification Date:
2025-12-25 @ 2:36 PM
NCT ID:
NCT00492050
Group ID:
EG000
Title:
All Participants
Description:
Bortezomib 1.6 mg/m\^2 IV Weekly on Days 1, 8, 15 and 22. Rituximab 375 mg/m\^2 IV on Day 8 and 22. Valacyclovir 500 mg orally daily (or acyclovir 200 mg orally twice daily).
Bortezomib: 1.6 mg/m\^2 IV Weekly on Days 1, 8, 15 and 22.
Rituximab: 375 mg/m\^2 IV on Day 8 and 22.
Valacyclovir: 500 mg orally daily (or acyclovir 200 mg orally twice daily)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
14
Serious Number At Risk:
37
Other Number Affected:
14
Other Number At Risk:
37
Study:
NCT00492050
Results Section:
NCT00492050
Adverse Events Module:
NCT00492050