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 @ 3:01 PM
Ignite Modification Date:
2025-12-25 @ 1:24 PM
NCT ID:
NCT04115059
Group ID:
EG000
Title:
Dasatinib
Description:
\-- After the screening procedures confirm participation in the research study: The participant will be given a study drug-dosing calendar for each treatment cycle.
Dasatinib: Oral Study Drug(s):
* Each study treatment cycle lasts 4 weeks during which time you will be taking the study drug one time per day.
* This will continue for up to 24 cycles.
Dasatinib: Oral, daily, dosing per protocol, once a day for cycle
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
3
Other Number Affected:
3
Other Number At Risk:
3
Study:
NCT04115059
Results Section:
NCT04115059
Adverse Events Module:
NCT04115059