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 @ 9:54 PM
Ignite Modification Date:
2025-12-25 @ 7:32 PM
NCT ID:
NCT00048932
Group ID:
EG001
Title:
Abatacept (ABA)
Description:
Participants received a fixed dose of abatacept approximating 10 mg/kg (500 mg for subjects \< 60 kg, 750 mg for subjects 60 to 100 kg and 1 g for subjects \> 100 kg). Abatacept was administered intravenously (IV) on Days 1, 15, 29, and every 28 days thereafter, for a total of 14 doses. Participants also received background therapy(ies) for rheumatoid arthritis (RA) (non-biologic or biologic disease-modifying drugs \[DMARDs\], or combination) throughout the double-blind treatment period.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
124
Serious Number At Risk:
959
Other Number Affected:
715
Other Number At Risk:
959
Study:
NCT00048932
Results Section:
NCT00048932
Adverse Events Module:
NCT00048932