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 @ 4:15 PM
Ignite Modification Date:
2025-12-25 @ 2:13 PM
NCT ID:
NCT04501666
Group ID:
EG000
Title:
Nemolizumab
Description:
Participants weighing \<90 kg received two SC injections of 30 mg nemolizumab (60 mg loading dose) at baseline then one SC injection Q4W. Participants weighing \>=90 kg received two SC injections of 30 mg nemolizumab (60 mg total) at baseline (no loading dose) and two SC injections Q4W throughout the treatment period of 16 weeks.
Nemolizumab: Participants received either 30 mg or 60 mg dose of nemolizumab as SC injection.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
16
Serious Number At Risk:
187
Other Number Affected:
61
Other Number At Risk:
187
Study:
NCT04501666
Results Section:
NCT04501666
Adverse Events Module:
NCT04501666