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 @ 12:09 PM
Ignite Modification Date:
2025-12-25 @ 11:59 AM
NCT ID:
NCT03169361
Group ID:
EG000
Title:
Ixazomib 4 mg
Description:
The usual adult dosage for oral administration was 4 mg as ixazomib, in the fasting state, once a day, once a week for 3 weeks (Days 1, 8, and 15), with a 13-day washout period (Days 16 through 28). This 4-week cycle was repeated for 6 cycles. The dose might be reduced appropriately according to the patient's condition. Participants received interventions as part of routine medical care.
Deaths Number Affected:
11
Deaths Number At Risk:
None
Serious Number Affected:
193
Serious Number At Risk:
742
Other Number Affected:
515
Other Number At Risk:
742
Study:
NCT03169361
Results Section:
NCT03169361
Adverse Events Module:
NCT03169361