Ignite Creation Date:
2024-05-05 @ 10:00 AM
Last Modification Date:
2024-10-26 @ 9:05 AM
Study NCT ID:
NCT00006459
Status:
COMPLETED
Last Update Posted:
2012-06-07
First Post:
2000-11-06
Brief Title:
Paclitaxel With or Without Gemcitabine in Treating Women With Advanced Breast Cancer
Sponsor:
Eli Lilly and Company
Organization:
Eli Lilly and Company
Study Overview
Official Title:
Phase III Study of Gemcitabine Plus Paclitaxel Versus Paclitaxel in Patients With Unresectable Locally Recurrent or Metastatic Breast Cancer
Status:
COMPLETED
Status Verified Date:
2002-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
RATIONALE Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die Combining more than one drug may kill more tumor cells It is not yet known if paclitaxel is more effective with or without gemcitabine for advanced breast cancer
PURPOSE Randomized phase III trial to study the effectiveness of paclitaxel with or without gemcitabine in treating women who have advanced breast cancer
PURPOSE Randomized phase III trial to study the effectiveness of paclitaxel with or without gemcitabine in treating women who have advanced breast cancer
Detailed Description:
OBJECTIVES I Compare overall survival of patients with unresectable locally recurrent or metastatic breast cancer treated with paclitaxel with or without gemcitabine
OUTLINE This is a randomized multicenter study Patients are randomized to one of two treatment arms Patients receive paclitaxel with or without gemcitabine Treatment continues every 21 days in the absence of disease progression Patients are followed every 2-4 months for 2 years after active treatment
PROJECTED ACCRUAL Not specified
National Cancer Institute NCI registered this trial with Eli Lilly as sponsor NCI did not update the record when the trial completed In June 2012 NCI transferred the trial to Lillys clinicaltrialsgov account and Lilly updated the record with the trial completion date This trial is not an applicable trial under Food and Drug Administration Amendments Act of 2007 FDAAA
OUTLINE This is a randomized multicenter study Patients are randomized to one of two treatment arms Patients receive paclitaxel with or without gemcitabine Treatment continues every 21 days in the absence of disease progression Patients are followed every 2-4 months for 2 years after active treatment
PROJECTED ACCRUAL Not specified
National Cancer Institute NCI registered this trial with Eli Lilly as sponsor NCI did not update the record when the trial completed In June 2012 NCI transferred the trial to Lillys clinicaltrialsgov account and Lilly updated the record with the trial completion date This trial is not an applicable trial under Food and Drug Administration Amendments Act of 2007 FDAAA
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| CDR0000068216 | None | None | None |
| LILLY-B9E-MC-JHQG | None | None | None |