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 @ 11:09 PM
Ignite Modification Date:
2025-12-25 @ 8:43 PM
NCT ID:
NCT05321069
Group ID:
EG001
Title:
Nera 9 mg BID
Description:
Participants received 9 mg film-coated nerandomilast tablets orally twice daily, with doses administered at least 12 hours apart, each taken with 250 mL of water.
Deaths Number Affected:
36
Deaths Number At Risk:
None
Serious Number Affected:
159
Serious Number At Risk:
392
Other Number Affected:
319
Other Number At Risk:
392
Study:
NCT05321069
Results Section:
NCT05321069
Adverse Events Module:
NCT05321069