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 @ 5:55 PM
Ignite Modification Date:
2025-12-25 @ 3:19 PM
NCT ID:
NCT03427268
Group ID:
EG000
Title:
PM060184
Description:
PM060184 was administered i.v. via a central line or a peripheral venous catheter (in 30-min administration) at a dose of 9.3 mg/m2 on Day 1 and Day 8 every three weeks (q3wk) (three weeks = one treatment cycle) (dose can be rounded to the first decimal point).
Deaths Number Affected:
16
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
30
Other Number Affected:
30
Other Number At Risk:
30
Study:
NCT03427268
Results Section:
NCT03427268
Adverse Events Module:
NCT03427268