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 @ 12:37 AM
Ignite Modification Date:
2025-12-25 @ 10:47 PM
NCT ID:
NCT01136967
Group ID:
EG000
Title:
Cohort 1 (V600E BRAF Negative)
Description:
Cohort 1 (V600E BRAF negative) enrolled participants not harboring the V600E BRAF mutation with disease progression following up to 2 prior systemic anticancer regimens (excluding anti-VEGF) for unresectable Stage III or Stage IV melanoma. Participants received lenvatinib 24 mg orally, once daily continuously in 28-day cycles.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
39
Serious Number At Risk:
93
Other Number Affected:
93
Other Number At Risk:
93
Study:
NCT01136967
Results Section:
NCT01136967
Adverse Events Module:
NCT01136967