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 @ 3:46 PM
Ignite Modification Date:
2025-12-25 @ 1:53 PM
NCT ID:
NCT00996892
Group ID:
EG010
Title:
S1A CD/S2A Expension: 125 mg Cobimetinib + 180 mg Pictilisib
Description:
Participants received cobimetinib 125 mg capsules on Days 1, 4, 8, 11, 15, and 18 and pictilisib 180 mg capsules from Days 1 to 21 and then 7 days off study drugs from Days 22 to 28 in continuous 28-day cycles. Treatment continued until disease progression, unacceptable toxicity, or any other discontinuation criterion was met. This arm included participants form S1A CD as well as S2A expansion cohort.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
28
Serious Number At Risk:
52
Other Number Affected:
52
Other Number At Risk:
52
Study:
NCT00996892
Results Section:
NCT00996892
Adverse Events Module:
NCT00996892