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 @ 12:09 AM
Ignite Modification Date:
2025-12-25 @ 10:09 PM
NCT ID:
NCT06768658
Group ID:
EG001
Title:
TAK-951 4 mg
Description:
Participants were to receive TAK-951 4 mg (Treatment B), injection, subcutaneously, single dose, on Day 1 in CVS Episodes 1, 2, 3, or 4 (Periods 1, 2, 3 or 4). A washout period of at least 14 days was planned to be maintained between each Period.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
0
Other Number Affected:
0
Other Number At Risk:
0
Study:
NCT06768658
Results Section:
NCT06768658
Adverse Events Module:
NCT06768658