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 @ 2:58 AM
Ignite Modification Date:
2025-12-26 @ 1:39 AM
NCT ID:
NCT03292133
Group ID:
EG000
Title:
EGF816 + Gefitinib
Description:
* All patients will receive gefitinib orally once daily
* EGF816 will be administered orally once daily
* Participant will be requested to maintain a medication diary of each dose of medication
EGF816: EGF816 is an inhibitor which target a specific mutation in cancer and may stop tumors growing and multiplying
Gefitinib: Gefitinib is an inhibitor which target a specific mutation in cancer and may stop tumors growing and multiplying
Deaths Number Affected:
4
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
11
Other Number Affected:
11
Other Number At Risk:
11
Study:
NCT03292133
Results Section:
NCT03292133
Adverse Events Module:
NCT03292133