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Clinical Trial Summary

Objectives:

- To determine the maximum tolerated dose of oral topotecan when administered with Temodar to patients with malignant glioma

- To characterize any toxicity associated with the combination oral topotecan and Temodar.

- To observe patients for clinical antitumor response when treated with oral topotecan and Temodar.


Clinical Trial Description

Subjects are patients with glioblastoma (GBM), anaplastic astrocytoma (AA) or grade 3 or greater WHO astrocytic, oligodendroglial or mixed glial tumors, which were initially diagnosed by histologic examination of biopsy/resection. Modified classical "3+3" phase I design used to determine maximum tolerated dose of topotecan in combination with Temodar. ;


Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00610571
Study type Interventional
Source Duke University
Contact
Status Completed
Phase Phase 1
Start date April 2004
Completion date April 2012

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