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 @ 10:37 PM
Ignite Modification Date:
2025-12-25 @ 8:09 PM
NCT ID:
NCT01834235
Group ID:
EG000
Title:
Arm A
Description:
Patients on arm A will receive Nab-paclitaxel at a dose of 125 mg/m2 as a 30 minute infusion followed by 1000 mg/m2 gemcitabine for 3 consecutive weeks followed by a week of rest (treatment on days 1, 8, and 15, during a 28-day cycle. NPC-1C (NEO-102) will be infused 30 minutes after completion of the gemcitabine infusion at a dose of 1.5mg/kg IV on days 1 and 15 of the 28 day cycle.
Deaths Number Affected:
38
Deaths Number At Risk:
None
Serious Number Affected:
18
Serious Number At Risk:
38
Other Number Affected:
32
Other Number At Risk:
38
Study:
NCT01834235
Results Section:
NCT01834235
Adverse Events Module:
NCT01834235