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 @ 4:09 AM
Ignite Modification Date:
2025-12-26 @ 3:06 AM
NCT ID:
NCT03375320
Group ID:
EG002
Title:
Arm Ib (Cabozantinib S-malate, Pancreatic NET Cohort [pNET])
Description:
Patients receive cabozantinib S-malate PO QD on days 1-28 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Patients also undergo CT, MRI, and/or x-ray imaging during screening and on study. \>
* Cabozantinib S-malate: Given PO \>
* Computed Tomography: Undergo CT \>
* Magnetic Resonance Imaging: Undergo MRI \>
* Quality-of-Life Assessment: Ancillary studies \>
* X-Ray Imaging: Undergo x-ray
Deaths Number Affected:
21
Deaths Number At Risk:
None
Serious Number Affected:
49
Serious Number At Risk:
64
Other Number Affected:
64
Other Number At Risk:
64
Study:
NCT03375320
Results Section:
NCT03375320
Adverse Events Module:
NCT03375320