Viewing Study NCT00191243



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Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00191243
Status: COMPLETED
Last Update Posted: 2019-09-12
First Post: 2005-09-12

Brief Title: Docetaxel vs Docetaxel-Gemcitabine in Breast Cancer
Sponsor: Eli Lilly and Company
Organization: Eli Lilly and Company

Study Overview

Official Title: A Randomized Phase II Study Comparing Single-Agent Docetaxel to Alternating Docetaxel-Gemcitabine as Primary Chemotherapy in Patients With Metastatic Breast Cancer
Status: COMPLETED
Status Verified Date: 2019-09
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: Randomizednon-blindedmulti-center study in patients with metastatic breast cancerPatients will be treated with docetaxel or docetaxel-gemcitabine

Aim of the study is to assess the optimal dosage and safety in this setting
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
Secondary IDs
Secondary ID Type Domain Link
B9E-MC-S241 OTHER Eli Lilly and Company None