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 @ 11:33 PM
Ignite Modification Date:
2025-12-25 @ 9:22 PM
NCT ID:
NCT02178956
Group ID:
EG000
Title:
Napabucasin + Paclitaxel
Description:
Napabucasin was administered orally, twice daily, with doses separated by 12 hours. Paclitaxel 80 mg/m2 (intravenous \[IV\]) was administered weekly, on Days 1, 8, and 15 of each 28 day study cycle. Napabucasin administration began 2 days prior to the first paclitaxel infusion in the initial run in period.
Deaths Number Affected:
286
Deaths Number At Risk:
None
Serious Number Affected:
125
Serious Number At Risk:
357
Other Number Affected:
352
Other Number At Risk:
357
Study:
NCT02178956
Results Section:
NCT02178956
Adverse Events Module:
NCT02178956