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 @ 10:36 PM
Ignite Modification Date:
2025-12-25 @ 8:08 PM
NCT ID:
NCT03314935
Group ID:
EG008
Title:
Phase 1 and Phase 2: INCB001158 100 mg + Paclitaxel
Description:
In Phases 1 and 2, participants with advanced or metastatic solid tumors (Phase 1) and GC, EC, or OC (Phase 2) received oral INCB001158 100 mg BID starting on Day 1 of each 28-day cycle. Participants with advanced or metastatic solid tumors (Phase 1) and with GC, EC, or OC (Phase 2) also received intravenous paclitaxel 80 mg/m\^2 on Day 1, Day 8, and Day 15 of each 28-day cycle.
Deaths Number Affected:
36
Deaths Number At Risk:
None
Serious Number Affected:
27
Serious Number At Risk:
52
Other Number Affected:
50
Other Number At Risk:
52
Study:
NCT03314935
Results Section:
NCT03314935
Adverse Events Module:
NCT03314935