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 @ 4:17 AM
Ignite Modification Date:
2025-12-26 @ 3:18 AM
NCT ID:
NCT02933320
Group ID:
EG000
Title:
Part A: Arm 1: BI-1206 Single Agent Dose Escalation Phase
Description:
BI-1206 given by IV infusion to all patients once weekly for a period of four weeks, patients will then have a follow-up period of four weeks (8 week period classified as induction therapy).
BI-1206 single agent dose escalation phase: BI-1206 single agent dose escalation phase to determine the MTD or MAD and RP2D for evaluation of BI-1206.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
10
Serious Number At Risk:
13
Other Number Affected:
13
Other Number At Risk:
13
Study:
NCT02933320
Results Section:
NCT02933320
Adverse Events Module:
NCT02933320