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 @ 11:10 PM
Ignite Modification Date:
2025-12-25 @ 8:44 PM
NCT ID:
NCT03086369
Group ID:
EG003
Title:
Phase 2: Olaratumab + Nab-paclitaxel + Gemcitabine
Description:
Participants received intravenous infusions of olaratumab 20 mg/kg loading dose on days 1, 8, 15 of cycle 1 followed by 15 mg/kg on days 1, 8, 15 of all subsequent cycles, in combination with nab-paclitaxel 125 mg/m\^2 and gemcitabine 1000 mg/m\^2 on days 1, 8, 15 of a 28-day cycle until disease progression or a criterion for discontinuation were met.
Deaths Number Affected:
60
Deaths Number At Risk:
None
Serious Number Affected:
50
Serious Number At Risk:
81
Other Number Affected:
79
Other Number At Risk:
81
Study:
NCT03086369
Results Section:
NCT03086369
Adverse Events Module:
NCT03086369