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 @ 10:29 PM
Ignite Modification Date:
2025-12-25 @ 8:03 PM
NCT ID:
NCT00451035
Group ID:
EG000
Title:
Panobinostat
Description:
Participants were administered panobinostat 20 mg orally OD three times a week as part of a 4 week (28 day) treatment cycle. Treatment were administered at the same time each morning with 240 ml of water after a fasting period of at least two hours (water was allowed). Participants could continue treatment until they experienced unacceptable toxicity or disease progression.
Deaths Number Affected:
3
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
29
Other Number Affected:
26
Other Number At Risk:
29
Study:
NCT00451035
Results Section:
NCT00451035
Adverse Events Module:
NCT00451035