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 @ 10:32 PM
Ignite Modification Date:
2025-12-25 @ 8:05 PM
NCT ID:
NCT01757535
Group ID:
EG001
Title:
Placebo Plus Best Supportive Care
Description:
Participants received identically matching placebo tablets QD for the first 14 days of each 28-day treatment cycle until no longer receiving benefit, withdrawal of consent, disease relapse, adverse events, participant became eligible for allogeneic bone marrow or stem cell transplantation during the treatment period, lost to follow-up, or protocol violation or until the end of the study.
Deaths Number Affected:
176
Deaths Number At Risk:
None
Serious Number Affected:
109
Serious Number At Risk:
233
Other Number Affected:
224
Other Number At Risk:
233
Study:
NCT01757535
Results Section:
NCT01757535
Adverse Events Module:
NCT01757535