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:
2025-12-24 @ 11:04 PM
Ignite Modification Date:
2025-12-25 @ 8:35 PM
NCT ID:
NCT03094169
Group ID:
EG007
Title:
Phase 2a Expansion: AVID100 220 mg/m^2
Description:
Participants from expanded populations of mTNBC, SCCHN, and Sq-NSCLC with documented EGFR expression received the maximum tolerated dose (MTD) determined in Phase 1, comprising AVID100 220 mg/m\^2 administered every 3 weeks IV, for at least 1 cycle. Extended treatment was permitted for participants tolerating and benefiting from treatment.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
13
Serious Number At Risk:
25
Other Number Affected:
25
Other Number At Risk:
25
Study:
NCT03094169
Results Section:
NCT03094169
Adverse Events Module:
NCT03094169