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:
2025-12-26 @ 10:17 PM
Ignite Modification Date:
2025-12-26 @ 10:17 PM
NCT ID:
NCT04175912
Group ID:
EG001
Title:
Arm B (Pevonedistat, Paclitaxel, Carboplatin)
Description:
Patients receive pevonedistat IV over 1 hour on days 1, 3, and 5, paclitaxel IV over 3 hours on day 1, and carboplatin IV over 15-60 minutes on day 1. Cycles repeat every 21 days in the absence of disease progression or unacceptable toxicity. Starting cycle 5, patients may receive pevonedistat monotherapy at the discretion of treating physician.
Deaths Number Affected:
15
Deaths Number At Risk:
None
Serious Number Affected:
12
Serious Number At Risk:
17
Other Number Affected:
17
Other Number At Risk:
17
Study:
NCT04175912
Results Section:
NCT04175912
Adverse Events Module:
NCT04175912