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 @ 2:39 AM
Ignite Modification Date:
2025-12-26 @ 1:17 AM
NCT ID:
NCT03312634
Group ID:
EG001
Title:
Palovarotene 20/10 mg
Description:
Participants with flare-up symptoms or traumatic events received palovarotene 20 mg once daily for 4 weeks after the flare-up confirmation by the Investigator. Followed by palovarotene 10 mg once daily for 8 weeks.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
81
Other Number Affected:
77
Other Number At Risk:
81
Study:
NCT03312634
Results Section:
NCT03312634
Adverse Events Module:
NCT03312634