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 @ 11:08 PM
Ignite Modification Date:
2025-12-25 @ 8:40 PM
NCT ID:
NCT04999969
Group ID:
EG000
Title:
AZD0171 + Durvalumab + Chemotherapy
Description:
Participants received AZD0171 (intravenous \[IV\]) along with durvalumab IV in combination with standard-of-care chemotherapy IV (gemcitabine and nab-paclitaxel) until disease progression, death, lost to follow-up or consent withdrawal which ever occurred first.
Deaths Number Affected:
76
Deaths Number At Risk:
None
Serious Number Affected:
72
Serious Number At Risk:
126
Other Number Affected:
126
Other Number At Risk:
126
Study:
NCT04999969
Results Section:
NCT04999969
Adverse Events Module:
NCT04999969