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 @ 4:02 PM
Ignite Modification Date:
2025-12-25 @ 2:04 PM
NCT ID:
NCT02057666
Group ID:
EG000
Title:
Tasquinimod
Description:
One capsule (0.25, 0.50 or 1 mg), taken orally once a day with water and food (preferably the main evening meal).
A patient initially received a 0.25 mg/day dose which was then titrated through 0.5 mg/day (from Day 15) to a maximum of 1 mg/day (from Day 29). If tolerability issues arose at 0.5 or 1 mg/day, patients had their dose reduced to 0.25 or 0.5 mg/day, respectively.
Deaths Number Affected:
76
Deaths Number At Risk:
None
Serious Number Affected:
19
Serious Number At Risk:
94
Other Number Affected:
52
Other Number At Risk:
94
Study:
NCT02057666
Results Section:
NCT02057666
Adverse Events Module:
NCT02057666