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 @ 12:22 AM
Ignite Modification Date:
2025-12-25 @ 10:26 PM
NCT ID:
NCT02990858
Group ID:
EG000
Title:
PRO 140 350 mg
Description:
Eligible subjects received 350 mg PRO 140 (leronlimab) administered weekly as subcutaneous injections along with Optimized Background Therapy (OBT) until virologic failure or another reason for discontinuation.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
11
Serious Number At Risk:
29
Other Number Affected:
27
Other Number At Risk:
29
Study:
NCT02990858
Results Section:
NCT02990858
Adverse Events Module:
NCT02990858