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 @ 4:14 AM
Ignite Modification Date:
2025-12-26 @ 3:14 AM
NCT ID:
NCT03834220
Group ID:
EG002
Title:
Cohort 3: Debio 1347 (All Other Solid Tumor Histologies)
Description:
Participants with all other solid tumor histologies were included in this cohort to receive Debio 1347 80 mg tablets, orally, QD, from Day 1 to Day 28 in 28-day cycles until the occurrence of disease progression or unacceptable toxicity (up to a median duration of 8.14 weeks).
Deaths Number Affected:
17
Deaths Number At Risk:
None
Serious Number Affected:
7
Serious Number At Risk:
29
Other Number Affected:
28
Other Number At Risk:
29
Study:
NCT03834220
Results Section:
NCT03834220
Adverse Events Module:
NCT03834220