At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 25 enrolled
Drug / intervention
Temozolomidedrug
Likely dose
Temozolomide 100 mg/m2from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Efficacy of a Protracted Temozolomide Schedule in Patients With Progression After Standard Dose Temozolomide for High-grade Gliomas
In Brief
A Phase 2 clinical trial evaluating Temozolomide for Glioblastoma and 3 related conditions. Completed, enrolled 25 participants across 1 site.
Detailed Summary
The purpose of this study is to evaluate the efficacy of temozolomide on a protracted schedule, after standard 5-day temozolomide regimen in patients with recurrent or progressive high grade glioma.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsGlioblastoma, Astrocytoma, Oligodendroglioma, Brain Tumor, Recurrent
CountriesTurkey (Türkiye)
CollaboratorsSchering-Plough
Timeline
Phase 2CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartAug 2006
First PostedDec 2007
Primary CompletionMar 2009
TodayJul 2026
First PostedDec 18, 2007
Enrollment StartAug 1, 2006
Primary CompletionMar 1, 2009
TodayJul 2, 2026
Enrollment to primary: 2.6 yearsPosted 18.5 years ago
Interventions
Temozolomidedrug
100 mg/m2/day, (PO) orally, on days between 1 and 21 of each 28 day cycles. Number of cycles: Until progression or unacceptable toxicity