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 @ 12:30 AM
Ignite Modification Date:
2025-12-25 @ 10:37 PM
NCT ID:
NCT00243867
Group ID:
EG000
Title:
Taxoprexin® and Carboplatin
Description:
Taxoprexin® 400 mg/m² intravenously weekly for 5 weeks
Carboplatin was given at an Area Under the Curve (AUC) = 4 mg\*min/mL on Week 1 and Week 4, Taxoprexin and carboplatin were given up to 3 treatment cycles.
Taxoprexin: Administered by intravenous infusion over 1 hour infusion
Carboplatin: Administered by intravenous infusion over 30 minutes. Dosing was based on the Calvert formula: carboplatin dose (mg) = (Target AUC) x (glomerular filtration rate \[GFR\] + 25).
Deaths Number Affected:
198
Deaths Number At Risk:
None
Serious Number Affected:
70
Serious Number At Risk:
256
Other Number Affected:
235
Other Number At Risk:
256
Study:
NCT00243867
Results Section:
NCT00243867
Adverse Events Module:
NCT00243867