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 @ 11:31 PM
Ignite Modification Date:
2025-12-25 @ 9:19 PM
NCT ID:
NCT00405756
Group ID:
EG000
Title:
MPR+R
Description:
Double-blind induction therapy with melphalan/prednisone and lenalidomide 10 mg (MPR) for up to 9 cycles, followed by maintenance therapy with single-agent lenalidomide (R) 10mg from cycle 10 to disease progression. Optional open-label extension therapy with lenalidomide up to 25 mg for participants with progressive disease.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
66
Serious Number At Risk:
150
Other Number Affected:
149
Other Number At Risk:
150
Study:
NCT00405756
Results Section:
NCT00405756
Adverse Events Module:
NCT00405756