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 @ 5:09 PM
Ignite Modification Date:
2025-12-25 @ 2:47 PM
NCT ID:
NCT02172950
Group ID:
EG000
Title:
CSL627: Previously Treated Patients (PTPs)
Description:
The investigator will assign subjects to either prophylaxis or on-demand treatment regimens for rVIII-SingleChain by intravenous injection. The investigator will determine the rVIII-SingleChain dose and dosing schedule for the subject based upon the subject's pharmacokinetic (PK) profile, rVIII-SingleChain PK data, previous FVIII treatment regimen, and bleeding phenotype, if available.
rVIII-SingleChain: Recombinant single-chain coagulation factor VIII
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
23
Serious Number At Risk:
222
Other Number Affected:
130
Other Number At Risk:
222
Study:
NCT02172950
Results Section:
NCT02172950
Adverse Events Module:
NCT02172950