Clinical Trials Directory

Trials / Completed

CompletedNCT00084214

STA-4783/Paclitaxel or Paclitaxel Alone in Melanoma

A Two-Stage Trial of STA-4783 in Combination With Weekly Paclitaxel for Treatment of Patients With Metastatic Melanoma

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
103 (planned)
Sponsor
Synta Pharmaceuticals Corp. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is designed to assess the efficacy of a weekly treatment regimen of STA-4783 and paclitaxel in comparison to paclitaxel alone on tumor response in metastatic melanoma patients.

Detailed description

STA-4783 is a taxane potentiator, enhancing the effect of antitumor response of paclitaxel. In an attempt to improve efficacy, paclitaxel is sometimes used in combination with other anticancer agents. When paclitaxel is combined with other anticancer agents, although response rate is usually increased, side effects are usually increased as well. There is an urgent need for agents that can enhance the antitumor effects of paclitaxel without further increasing undesirable side effects.

Conditions

Interventions

TypeNameDescription
DRUGSTA-4783
DRUGPaclitaxel

Timeline

Start date
2004-05-01
First posted
2004-06-10
Last updated
2014-03-06

Locations

28 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00084214. Inclusion in this directory is not an endorsement.