Viewing Study NCT00183885



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Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00183885
Status: UNKNOWN
Last Update Posted: 2018-05-16
First Post: 2005-09-09

Brief Title: A Phase II Study of Intra-arterial Chemotherapy With Cisplatin and Mitomycin-C in Patients With Hepatocellular Carcinoma
Sponsor: University of Southern California
Organization: University of Southern California

Study Overview

Official Title: A Phase II Study of Intra-arterial Chemotherapy With Cisplatin and Mitomycin-C
Status: UNKNOWN
Status Verified Date: 2018-05
Last Known Status: ACTIVE_NOT_RECRUITING
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: This study is for people with cancer of the liver that cannot be completely removed by surgery This study involves giving the drugs mitomycin-C and cisplatin into an artery in the liver Mitomycin-C is a drug that has been approved by the FDA to treat cancer of the stomach and pancreas Mitomycin-C is a drug that causes cancer cells to die and prevents them from reproducing Cisplatin is also a drug that has been approved by the FDA Cisplatin is approved to treat cancer of the testes ovaries lung esophagus bladder head and neck Cisplatin is a drug that prevents cancer cells from reproducing The purpose of this study is to see how long it takes subjects tumors to grow after receiving the study drugs Another purpose of this study is to look at the side effects of this study therapy and how long subjects survive after receiving it

An additional purpose of this study is to see how well we can predict subjects response to the study therapy based on blood and tumor tissue tests These tests will measure the levels of genes the cells blueprint in subjects tumors and blood These genes affect how peoples bodies react to the cancer drugs
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?: None