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:
2025-12-25 @ 2:43 AM
Ignite Modification Date:
2025-12-26 @ 1:22 AM
NCT ID:
NCT00520533
Group ID:
EG000
Title:
cG250 + Sunitinib
Description:
Treatment (cycle 1):
* cG250 10mg/m² IV weekly x 5 doses (1st \& 5th doses trace-labelled with 124I)
* Sunitinib 50 mg/day orally x 4 weeks commencing day 8
* Followed by two-week break
Treatment (cycle 2 - investigator discretion):
* cG250 10mg/m² IV weekly x4 doses
* Sunitinib 50 mg/day orally x 4 weeks (commencing concurrently)
* Followed by two-week break
Up to 2 cycles available on-study.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
6
Other Number Affected:
6
Other Number At Risk:
6
Study:
NCT00520533
Results Section:
NCT00520533
Adverse Events Module:
NCT00520533