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

StatusCompleted
PhasePhase 2
Started

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Record History

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  1. Study Status, Referencesv9
  2. Notable Primary and study completion dates changed from estimate of Sep 2010 to Jun 2011
    • Trial status: Active, Not Recruiting to Completed
    v8
  3. Minor Trial status: Recruiting to Active, Not Recruiting
    • Primary completion date: Sep 2010
    • Study completion date: Dec 2008 to Sep 2010
    • Site details revised at 2 of 2 sites
    v7
  4. Minor Study completion date: Dec 2007 to Dec 2008
    • Secondary endpoints: details revised at 3 of 3 entries
    v6
  5. Minor Study completion date: Jun 2006 to Dec 2007
    • Site contacts updated at 1 of 2 sites
    v5
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  1. Minor Study sites: 1 to 2
    • Collaborators expanded, about 2 words
    v4
  2. Minor Eligibility criteria expanded, about 1 wordv3
  3. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date: Oct 2005
    • Site details revised
    v2
  1. Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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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.
Trial Details
NCT Number NCT00209989
Lead Sponsor Institut Claudius Regaud
Collaborators: Janssen-Cilag Ltd.
Conditions
(from sponsor)
Glioblastoma Multiforme
Related terms Glioblastoma
Enrollment 27 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov