drugset / Trial / NCT00470613

Safety Study of Infusion of SGT-53 to Treat Solid Tumors

NCT00470613

Phase 1 Completed 25 enrolled SynerGene Therapeutics, Inc.
NaSingle-groupOpen-labelTreatment

Summary

This is a Phase Ib study as a continuation of the original Phase I protocol. The purpose of this Phase Ib study is to evaluate the safety of a single course of SGT-53 in combination with docetaxel and determine the recommended Phase II doses of SGT-53 and docetaxel in combination for evaluation in subsequent clinical studies for the treatment of solid tumors.

Timeline

Start
2008-02
Primary completion
2016-12
Completion
2016-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Docetaxel Small molecule 40 mg/m2
Subject Docetaxel Small molecule 60 mg/m2
Subject Docetaxel Small molecule 75 mg/m2
Subject SGT-53 Other / unclassified 2.4 mg Other
Subject SGT-53 Other / unclassified 3.6 mg Other

Indications