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 @ 9:22 PM
Ignite Modification Date:
2025-12-25 @ 7:08 PM
NCT ID:
NCT02102204
Group ID:
EG000
Title:
Etelcalcetide
Description:
Participants received etelcalcetide three times a week (TIW) by bolus injection at the end of hemodialysis. The minimum etelcalcetide dose in this study was 2.5 mg and the maximum dose was 15 mg. Etelcalcetide dose was titrated to maintain parathyroid hormone levels within 2x to 9x the upper limit of normal based on the reference range of the assay used at the individual study center.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
436
Serious Number At Risk:
884
Other Number Affected:
519
Other Number At Risk:
884
Study:
NCT02102204
Results Section:
NCT02102204
Adverse Events Module:
NCT02102204