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 @ 2:44 AM
Ignite Modification Date:
2025-12-26 @ 1:23 AM
NCT ID:
NCT04511533
Group ID:
EG000
Title:
Dacomitinib
Description:
Participants with metastatic non-small cell lung carcinoma (NSCLC) with epidermal growth factor receptor (EGFR) mutations received a starting dose of dacomitinib 45 mg once daily in each cycle of 28 days, until disease progression, participant refusal/lost to follow-up, or unacceptable toxicity occurred. The maximum treatment duration was approximately 107.3 weeks.
Deaths Number Affected:
9
Deaths Number At Risk:
None
Serious Number Affected:
16
Serious Number At Risk:
101
Other Number Affected:
93
Other Number At Risk:
101
Study:
NCT04511533
Results Section:
NCT04511533
Adverse Events Module:
NCT04511533