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 @ 5:08 AM
Ignite Modification Date:
2025-12-26 @ 4:12 AM
NCT ID:
NCT05067127
Group ID:
EG002
Title:
Open-Label Period: Pegcetacoplan to Pegcetacoplan
Description:
All eligible adult subjects (regardless of weight) and adolescent subjects with body weight \>=50 kg who received pegcetacoplan in RCP continued to receive pegcetacoplan 1080 mg SC infusion twice weekly for 26 weeks in OLP.
Eligible adolescent subjects with body weight 35 to \<50 kg who received pegcetacoplan in RCP continued to receive pegcetacoplan 810 mg SC infusion twice weekly for 26 weeks in OLP.
Eligible adolescent subjects with body weight 30 to \<35 kg who received pegcetacoplan in RCP continued to receive pegcetacoplan 648 mg SC infusion twice weekly for 26 weeks in OLP.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
6
Serious Number At Risk:
61
Other Number Affected:
47
Other Number At Risk:
61
Study:
NCT05067127
Results Section:
NCT05067127
Adverse Events Module:
NCT05067127