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Clinical Trial Summary

This phase I/II, multi-centered, non-randomized trial is designed to determine a safe dose of PT-523 for subjects, and to make preliminary evaluations on the activity of PT-523 as therapy in subjects with NSCLC.


Clinical Trial Description

n/a


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 NCT00112060
Study type Interventional
Source Spectrum Pharmaceuticals, Inc
Contact
Status Withdrawn
Phase Phase 1/Phase 2
Start date April 2008
Completion date September 2011

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