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 @ 12:40 AM
Ignite Modification Date:
2025-12-25 @ 10:51 PM
NCT ID:
NCT02927067
Group ID:
EG000
Title:
Valganciclovir 900 mg BID
Description:
Participants received 900 mg of valganciclovir along with a placebo matched to maribavir, BID orally for 8 weeks. Valganciclovir dose was allowed to be adjusted to 450 mg BID or 450 mg QD based on renal function impairment assessed at baseline or development of neutropenia during the study.
Deaths Number Affected:
29
Deaths Number At Risk:
None
Serious Number Affected:
95
Serious Number At Risk:
274
Other Number Affected:
256
Other Number At Risk:
274
Study:
NCT02927067
Results Section:
NCT02927067
Adverse Events Module:
NCT02927067