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Clinical Trial Summary

The purpose of this study is to determine the maximum tolerated dose of the TLC D-99 combined with ifosfamide and then the efficacy of this combination in terms of overall response rate, time to progression and time of response


Clinical Trial Description

The Maximum Tolerated Dose of the combination was determined and the Phase I terminated.

Then, Phase II study started. ;


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00289809
Study type Interventional
Source Istituto Clinico Humanitas
Contact
Status Completed
Phase Phase 1/Phase 2
Start date September 2006
Completion date December 2009

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