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 @ 12:34 AM
Ignite Modification Date:
2025-12-25 @ 10:43 PM
NCT ID:
NCT04522167
Group ID:
EG002
Title:
FYB203 (Proposed Aflibercept Biosimilar), Ocular AE, Study Eye
Description:
Patients will receive intravitreal (IVT) injections of FYB203 as detailed in the protocol.
FYB203 (Proposed aflibercept biosimilar): Patients will receive 1 IVT injection of FYB203 in the study eye only every 4 weeks for the first 3 consecutive doses, followed by 1 IVT injection every 8 weeks through study completion.
In this column all ocular AEs by patient for the FYB203 group occurring in the study eye are given.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
215
Other Number Affected:
44
Other Number At Risk:
215
Study:
NCT04522167
Results Section:
NCT04522167
Adverse Events Module:
NCT04522167