Viewing Study NCT01589094



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Last Modification Date: 2024-10-26 @ 10:50 AM
Study NCT ID: NCT01589094
Status: COMPLETED
Last Update Posted: 2019-10-02
First Post: 2012-04-27

Brief Title: Neoadjuvant Dose Dense Gemcitabine and Cisplatin DD GC In Patients With Muscle-Invasive Bladder Cancer
Sponsor: Memorial Sloan Kettering Cancer Center
Organization: Memorial Sloan Kettering Cancer Center

Study Overview

Official Title: Phase II Study of Neoadjuvant Dose Dense Gemcitabine and Cisplatin DD GC In Patients With Muscle-Invasive Bladder Cancer
Status: COMPLETED
Status Verified Date: 2018-08
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: The purpose of this study is to find out if standard chemotherapy gemcitabine and cisplatin given on a dose-dense treatment schedule with less time between treatments can help shrink the tumor better than standard chemotherapy given on a standard treatment schedule before the patient undergoes surgery for bladder cancer
Detailed Description: None

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