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 @ 3:32 AM
Ignite Modification Date:
2025-12-26 @ 2:14 AM
NCT ID:
NCT01871805
Group ID:
EG002
Title:
Alectinib 600 mg (Fed): Phase I
Description:
Participants received single dose of 20 or 40 or 150 mg alectinib capsules orally to make a dose of 600 mg on Cycle 1 Day -3 and then received 600 mg BID dose for 3-weekly cycles until disease progression, death or withdrawal for any other reasons.
Deaths Number Affected:
6
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
13
Other Number Affected:
12
Other Number At Risk:
13
Study:
NCT01871805
Results Section:
NCT01871805
Adverse Events Module:
NCT01871805