Viewing StudyNCT00191971



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Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00191971
Status: COMPLETED
Last Update Posted: 2007-11-06
First Post: 2005-09-12

Brief Title: 2nd Line Gemcitabine Monotherapy for Transitional Cell Carcinoma of Urothelium TCC After CDDP Regimen
Sponsor:
Organization: Eli Lilly and Company

Study Design

Study Type: INTERVENTIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: None
Target Duration: None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention: None
Bio Spec Description: None
Enrollment Count: 40
Enrollment Type: None
Design Primary Purpose:
Design Masking:
Phases:
Name
PHASE2
Observational Models:
Time Perspective List:
Who Masked List: