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 @ 4:19 AM
Ignite Modification Date:
2025-12-26 @ 3:20 AM
NCT ID:
NCT01752920
Group ID:
EG003
Title:
Derazantinib 300 mg QD - Expanded Cohort Group
Description:
Patients who received derazantinib orally at the recommended phase 2 dose of 300 mg QD on a 28-day schedule until documented progression of disease (clinical or radiological), unacceptable toxicity, or another of the discontinuation criteria.
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
16
Serious Number At Risk:
58
Other Number Affected:
58
Other Number At Risk:
58
Study:
NCT01752920
Results Section:
NCT01752920
Adverse Events Module:
NCT01752920