Viewing Study NCT00329329



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Last Modification Date: 2024-10-26 @ 9:25 AM
Study NCT ID: NCT00329329
Status: TERMINATED
Last Update Posted: 2012-03-23
First Post: 2006-05-22

Brief Title: Study of Satraplatin With Capecitabine to Treat Advanced Solid Malignancies
Sponsor: Agennix
Organization: Agennix

Study Overview

Official Title: Phase 1 Study of the Oral Platinum Agent Satraplatin in Combination With Capecitabine for the Treatment of Patients With Advanced Solid Malignancies
Status: TERMINATED
Status Verified Date: 2012-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Sponsor decided to discontinue study drug development
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 determine the maximally tolerated dose MTD and Phase 2 recommended dose of satraplatin when administered in combination with capecitabine in patients with advanced solid malignancies
Detailed Description: This is a single center open-label non-randomized Phase I dose finding study of the investigational oral cytotoxic drug satraplatin in combination with capecitabine in patients with advanced solid tumors for whom curative therapy is not available Please refer to the Eligibility Criteria below for key inclusion and exclusion criteria

PURPOSE The purpose of this trial is to determine a tolerable dose and schedule for the combination of satraplatin and docetaxel when given to patients with advanced solid tumors

WHAT IS SATRAPLATIN Satraplatin is an oral investigational anticancer drug that is a member of the platinum-based class of chemotherapy drugs Platinum-based drugs have been clinically proven to be one of the most effective classes of anticancer therapies Unlike the currently marketed platinum-based drugs satraplatin can be given orally

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