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 @ 9:22 PM
Ignite Modification Date:
2025-12-25 @ 7:08 PM
NCT ID:
NCT03020004
Group ID:
EG000
Title:
Danoprevir,Ritonavir, Peg-IFN,RBV
Description:
Participants will receive a combination of Ritonavir-boosted Danoprevir 100mg/100mg BID, subcutaneous injection of weekly peginterferon alfa-2a at 180 mcg and oral Ribavirin (RBV)1000/1200 mg/day (bodyweight\<75/≥75 kg) for 12 weeks.
Danoprevir: Danoprevir (DNV) 100mg tablet administered orally twice daily
Ritonavir: Ritonavir 100mg tablet administered orally twice daily
peginterferon alfa-2a: PegIFN subcutaneous injection at 180 mcg weekly
Ribavirin (RBV): Ribavirin (RBV)1000/1200 mg/day (bodyweight\<75/≥75 kg)
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
70
Other Number Affected:
70
Other Number At Risk:
70
Study:
NCT03020004
Results Section:
NCT03020004
Adverse Events Module:
NCT03020004