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 @ 10:58 PM
Ignite Modification Date:
2025-12-25 @ 8:27 PM
NCT ID:
NCT01743469
Group ID:
EG000
Title:
Hepatocellular Carcinoma Cohort
Description:
1 capsule of tasquinimod (0.25 mg or 0.5 mg or 1 mg) taken orally each day until disease progression, lost to follow-up, withdrawal or death.
1 capsule: initially at 0.5 mg/day, increasing to 1 mg/day, maintaining 0.5 mg/day or decreasing to 0.25 mg/day after at least 2 weeks.
Deaths Number Affected:
38
Deaths Number At Risk:
None
Serious Number Affected:
14
Serious Number At Risk:
53
Other Number Affected:
53
Other Number At Risk:
53
Study:
NCT01743469
Results Section:
NCT01743469
Adverse Events Module:
NCT01743469