Ignite Creation Date:
2024-05-05 @ 5:33 PM
Last Modification Date:
2024-10-26 @ 9:33 AM
Study NCT ID:
NCT00480935
Status:
TERMINATED
Last Update Posted:
2015-12-09
First Post:
2007-05-29
Brief Title:
A Study of Neoadjuvant Sutent for Patients With Renal Cell Carcinoma
Sponsor:
University Health Network Toronto
Organization:
University Health Network Toronto
Study Overview
Official Title:
A Phase II Single Arm Prospective Study of Neoadjuvant Sutent for Patients With Renal Cell Carcinoma
Status:
TERMINATED
Status Verified Date:
2015-12
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
poor recruitment
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Study Hypothesis Patients with local renal cell carcinoma who are treated neoadjuvantly with Sutent may show a radiologic response to the study drug Sutent
The study is looking at the neoadjuvant pre-surgery administration of Sutent in patients with localized kidney cancer The purpose of this research is also to evaluate both the safety and effectiveness of Sutent in this patient population
The study is looking at the neoadjuvant pre-surgery administration of Sutent in patients with localized kidney cancer The purpose of this research is also to evaluate both the safety and effectiveness of Sutent in this patient population
Detailed Description:
Sutent will be given at 50 mg once daily for 4 consecutive weeks followed by a 1 week rest period The dosage may change during the cycle due to possible drug toxicities The nephrectomy will then take place following a one-week washout period After surgery patients will have follow-up visits at 6 weeks and 3 months Patients will be followed for 3 years after completions to assess late toxicities time to progression and progression-free survival
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