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 @ 7:41 PM
Ignite Modification Date:
2025-12-25 @ 5:20 PM
NCT ID:
NCT02362503
Group ID:
EG002
Title:
Non-randomized Cohort-fostemsavir 600 mg BID
Description:
This reporting group includes HTE HIV-1 infected participants who were assigned to the Non-randomized Cohort and received fostemsavir 600 mg BID and OBT. Non-randomized Cohort participants are assigned based on their screening status of having no remaining classes of fully active antiretroviral that can combined in a new drug regimen. The data reported are safety events during fostemsavir dosing until the Week 96 data cut-off date.
Deaths Number Affected:
17
Deaths Number At Risk:
None
Serious Number Affected:
48
Serious Number At Risk:
99
Other Number Affected:
92
Other Number At Risk:
99
Study:
NCT02362503
Results Section:
NCT02362503
Adverse Events Module:
NCT02362503