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 @ 10:52 PM
Ignite Modification Date:
2025-12-25 @ 8:21 PM
NCT ID:
NCT03705169
Group ID:
EG004
Title:
Arm A: 0 mg/kg SAR441236
Description:
Placebo participants were pooled across those receiving:
* 1 mg/kg dose volume-equivalent administered as a single IV infusion (Cohort 1).
* 3 mg/kg dose volume-equivalent administered as a single IV infusion (Cohort 2).
* 10 mg/kg dose volume-equivalent administered as a single IV infusion (Cohort 3)
* 30 mg/kg dose volume-equivalent administered as an IV infusion on Day 0 and then every 12 weeks for a total of four doses (Cohort 4)
All continued on non-study provided ART.
Placebo: Administered by intravenous (IV) infusion(s) or subcutaneous (SC) injection(s)
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
10
Other Number Affected:
8
Other Number At Risk:
10
Study:
NCT03705169
Results Section:
NCT03705169
Adverse Events Module:
NCT03705169