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 @ 5:19 PM
Ignite Modification Date:
2025-12-25 @ 2:55 PM
NCT ID:
NCT02384850
Group ID:
EG000
Title:
Selinexor 40mg + mFOLFOX6
Description:
Selinexor: Dose Level 1: 40 mg on day 1, 3 and 8 in a two-weeks cycle.
Oxaliplatin: 85 mg/m² IV over 2 hours, Day 1 of a two-weeks cycle
5-FU: 400 mg/m² IV bolus, Day 1 of a two-weeks cycle 2,400 mg/m² continuous infusion IV, Days 1-3
Folinic Acid: 400 mg/m2 IV over 2 hours, Day 1 of a two-weeks cycle
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
4
Other Number Affected:
4
Other Number At Risk:
4
Study:
NCT02384850
Results Section:
NCT02384850
Adverse Events Module:
NCT02384850