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:
EG001
Title:
Randomized Cohort-fostemsavir 600 mg BID
Description:
Eligible participants in the Randomized Cohort had one to two fully active antiretrovirals remaining at Baseline. Participants received fostemsavir 600 milligram (mg) BID along with currently failing antiretroviral regimen for 8 days during the randomized, double-blind period. During the open-label period, all participants continued to receive fostemsavir 600 mg BID with an OBT.
Deaths Number Affected:
10
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
203
Other Number Affected:
45
Other Number At Risk:
203
Study:
NCT02362503
Results Section:
NCT02362503
Adverse Events Module:
NCT02362503