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 @ 4:18 PM
Ignite Modification Date:
2025-12-25 @ 2:15 PM
NCT ID:
NCT04681066
Group ID:
EG001
Title:
Auxora 1.0 mg/kg (0.625 mL/kg)
Description:
Medium dose Auxora, administered intravenously over 4 hours at a constant rate of infusion. Infusions were administered every 24 hours (±1 hour) for three consecutive days for a total of 3 doses.
CM-4620 Injectable Emulsion (CM4620-IE): Auxora is to be administered as an IV infusion and is supplied as a sterile, non-pyrogenic emulsion containing 1.6 mg/mL of the active pharmaceutical ingredient CM4620. CM4620-IE is supplied as an 80 mL fill in a 100 mL, single-use glass vial.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
12
Serious Number At Risk:
56
Other Number Affected:
32
Other Number At Risk:
56
Study:
NCT04681066
Results Section:
NCT04681066
Adverse Events Module:
NCT04681066