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 @ 10:49 PM
Ignite Modification Date:
2025-12-25 @ 8:19 PM
NCT ID:
NCT02657369
Group ID:
EG000
Title:
Lenvatinib
Description:
Participants received lenvatinib 24 mg (two 10-mg capsules and one 4-mg capsule), orally, once daily in a 28-days treatment cycle up to disease progression, development of unacceptable toxicity, lost to follow up, withdrawal of consent, participant's choice, pregnancy, or study termination by sponsor (approximately 27 months).
Deaths Number Affected:
27
Deaths Number At Risk:
None
Serious Number Affected:
25
Serious Number At Risk:
34
Other Number Affected:
32
Other Number At Risk:
34
Study:
NCT02657369
Results Section:
NCT02657369
Adverse Events Module:
NCT02657369