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 @ 2:19 PM
Ignite Modification Date:
2025-12-25 @ 12:56 PM
NCT ID:
NCT03177395
Group ID:
EG003
Title:
Group C: PP100-01 (Calmangafodipir 10 Umol/kg)+ NAC
Description:
In addition to the standard care NAC regime, participants will be allocated into a dosing cohort to receive:
PP100-01 (5 umol/kg calmangafodipir) after the "loading" dose of NAC
PP100-01 (10 umol/kg calmangafodipir) after the "loading" dose of NAC
PP100-01 treatment is administered intravenously over 5 minutes.
PP100-01 (calmangafodipir): PP100-01
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
3
Serious Number At Risk:
6
Other Number Affected:
6
Other Number At Risk:
6
Study:
NCT03177395
Results Section:
NCT03177395
Adverse Events Module:
NCT03177395