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 @ 9:19 PM
Ignite Modification Date:
2025-12-25 @ 7:06 PM
NCT ID:
NCT02713204
Group ID:
EG001
Title:
REGN910-3 6 mg:2 mg
Description:
Participants were administered intravitreal injection of REGN910-3 (6 mg:2 mg) Q4 on Day 1, Week 4 and Week 8 for 3 initial doses. At Week 12, participants were re-randomized to receive REGN910-3 (6 mg:2 mg) Q8 or Q12 (beginning at Week 16 or Week 20) through Week 32.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
20
Serious Number At Risk:
122
Other Number Affected:
41
Other Number At Risk:
122
Study:
NCT02713204
Results Section:
NCT02713204
Adverse Events Module:
NCT02713204