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 @ 12:23 PM
Ignite Modification Date:
2025-12-25 @ 12:03 PM
NCT ID:
NCT02215161
Group ID:
EG000
Title:
Treatment (Selinexor)
Description:
BID: twice a day D: day PO: oral 1 cycle = 4 weeks, 28 days
Premedication:
* Ondansetron 8 mg PO every 8 hours on day prior to and day of dosing (D0-D3)
* Olanzapine 5 mg PO at bedtime or 2.5 mg PO BID on day of dosing (D1, D3)
Study drug:
\- Selinexor PO on D1 and D3 of weeks 1-3 of each cycle. Drug holiday on week 4. Courses repeat every 28 days in absence of disease progression or unacceptable toxicity.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
14
Other Number Affected:
13
Other Number At Risk:
14
Study:
NCT02215161
Results Section:
NCT02215161
Adverse Events Module:
NCT02215161