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 @ 1:26 AM
Ignite Modification Date:
2025-12-25 @ 11:37 PM
NCT ID:
NCT02856893
Group ID:
EG001
Title:
Gefitinib Till + Blood Test/Progression Than Osimertinib
Description:
Gefitinib until emergence of positive T790M status ("cfDNA T790M positive progression") followed by Osimertinib until second PD according to RECIST 1.1
Osimertinib: Osimertinib 60 or 40 mg daily until progression
Gefitinib: Gefitinib 250mg daily until progression
Deaths Number Affected:
20
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
52
Other Number Affected:
51
Other Number At Risk:
52
Study:
NCT02856893
Results Section:
NCT02856893
Adverse Events Module:
NCT02856893