Ignite Creation Date:
2024-05-05 @ 4:38 PM
Last Modification Date:
2024-10-26 @ 9:22 AM
Study NCT ID:
NCT00287859
Status:
TERMINATED
Last Update Posted:
2017-11-29
First Post:
2006-02-06
Brief Title:
Topotecan in Treating Patients With Ovarian Epithelial Fallopian Tube or Primary Peritoneal Cavity Cancer
Sponsor:
Masonic Cancer Center University of Minnesota
Organization:
Masonic Cancer Center University of Minnesota
Study Overview
Official Title:
Phase I Study of Weekly Topotecan in Women With Progressive or Recurrent Ovarian Cancer and a Poor Performance Status
Status:
TERMINATED
Status Verified Date:
2017-11
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Withdrawn due to low accrual
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 such as topotecan work in different ways to stop the growth of tumor cells either by killing the cells or by stopping them from dividing Chemotherapy drugs may have different effects in patients who have a poor performance status
PURPOSE This phase I trial is studying the side effects and best dose of topotecan in treating patients with progressive or recurrent ovarian epithelial fallopian tube or primary peritoneal cavity cancer with a poor performance status
PURPOSE This phase I trial is studying the side effects and best dose of topotecan in treating patients with progressive or recurrent ovarian epithelial fallopian tube or primary peritoneal cavity cancer with a poor performance status
Detailed Description:
OBJECTIVES
Primary
Determine the maximum tolerated dose of weekly topotecan in patients with progressive or recurrent ovarian epithelial fallopian tube or primary peritoneal cavity cancer and a poor performance status
Secondary
Estimate the response rate of women with poor performance status for use in future clinical trials
OUTLINE This is a dose-escalation study
Patients receive topotecan intravenously IV over 30 minutes on days 1 8 15 22 and 29 Treatment repeats every 42 days for up to 6 courses in the absence of disease progression or unacceptable toxicity
Cohorts of 3-6 patients receive escalating doses of topotecan until the maximum tolerated dose MTD is determined The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity A total of 6 patients will be treated at the MTD
Patients are followed periodically for up to 2 years
Primary
Determine the maximum tolerated dose of weekly topotecan in patients with progressive or recurrent ovarian epithelial fallopian tube or primary peritoneal cavity cancer and a poor performance status
Secondary
Estimate the response rate of women with poor performance status for use in future clinical trials
OUTLINE This is a dose-escalation study
Patients receive topotecan intravenously IV over 30 minutes on days 1 8 15 22 and 29 Treatment repeats every 42 days for up to 6 courses in the absence of disease progression or unacceptable toxicity
Cohorts of 3-6 patients receive escalating doses of topotecan until the maximum tolerated dose MTD is determined The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity A total of 6 patients will be treated at the MTD
Patients are followed periodically for up to 2 years
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 |
|---|---|---|---|
| UMN-WCC-39 | OTHER | Womens Cancer Center University of Minnesota | None |