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 @ 4:30 AM
Ignite Modification Date:
2025-12-26 @ 3:33 AM
NCT ID:
NCT00436618
Group ID:
EG000
Title:
Relapsed Aggressive Non-Hodgkin Lymphoma
Description:
Study 1.
Everolimus 10 mg orally daily for 4 week cycle. Repeat until progression, unacceptable toxicity, refusal, or alternative therapy at any time.
Everolimus : Everolimus 10 mg orally daily for 4 week cycle. Repeat until progression, unacceptable toxicity, refusal, or alternative therapy at any time.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
38
Serious Number At Risk:
114
Other Number Affected:
113
Other Number At Risk:
114
Study:
NCT00436618
Results Section:
NCT00436618
Adverse Events Module:
NCT00436618