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COMPLETED
NCT00209989
PHASE2

Phase II Trial to Assess the Radiosensitizing Effect of ZARNESTRA in Patients With Glioblastoma Multiforme

Sponsor: Institut Claudius Regaud

View on ClinicalTrials.gov

Summary

The purpose of this study is to determine the efficacy by the determination of the Time To Progression (TTP) in patients with resectable GBM or non surgical GBM with a size less than 5 cm treated with the combination of ZARNESTRA plus Radiation therapy.

Official title: Phase I/II Trial to Assess the Radiosensitizing Effect of ZARNESTRA in Patients With Glioblastoma Multiforme

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

27

Start Date

2005-10

Completion Date

2011-06

Last Updated

2026-06-26

Healthy Volunteers

No

Interventions

DRUG

Zarnestra

ZARNESTRA 100 bid (phase II recommended dose defined in phase I)will be administered continuously from one week prior to start of radiation therapy until the last day of radiation therapy.

PROCEDURE

standard Radiation therapy

Radiotherapy will be focused on the initial tumour volume with a reasonable margin of safety (2 cm). A total dose of 60 Gray (Gy) will be given to the Clinical Target Volume

Locations (2)

Centre Jean Perrin

Clermont-Ferrand, France

Institut Claudius Regaud

Toulouse, France