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:
2025-12-26 @ 10:58 AM
Ignite Modification Date:
2025-12-26 @ 10:58 AM
NCT ID:
NCT01382706
Group ID:
EG000
Title:
Treatment
Description:
Patients receive docetaxel IV over 1 hour on day 1 and lapatinib ditosylate PO QD on days 1-21. Courses repeat every 21 days until disease progression or unacceptable toxicity.
docetaxel: Given IV
lapatinib ditosylate: Given PO
immunohistochemistry staining method: Correlative studies
fluorescence in situ hybridization: Correlative studies
laboratory biomarker analysis: Correlative studies
Deaths Number Affected:
11
Deaths Number At Risk:
None
Serious Number Affected:
15
Serious Number At Risk:
15
Other Number Affected:
15
Other Number At Risk:
15
Study:
NCT01382706
Results Section:
NCT01382706
Adverse Events Module:
NCT01382706