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Sponsored by: |
Schering-Plough |
Information provided by: | Schering-Plough |
ClinicalTrials.gov Identifier: | NCT00723827 |
The purpose of this surveillance is to evaluate the postmarketing safety and efficacy of Temodal capsule (temozolomide) under actual conditions of use, and to understand some points in question and doubt:
Condition | Intervention |
Glioblastoma Glioma Astrocytoma |
Drug: Temozolomide Radiation: Radiotherapy |
MedlinePlus related topics: | Cancer |
Drug Information available for: | Temozolomide |
Study Type: | Observational |
Study Design: | Cohort, Prospective |
Official Title: | Temodal (Temozolomide) Post Marketing Surveillance Protocol |
Estimated Enrollment: | 900 |
Study Start Date: | March 2008 |
Estimated Study Completion Date: | October 2011 |
Estimated Primary Completion Date: | October 2011 (Final data collection date for primary outcome measure) |
Groups/Cohorts | Assigned Interventions |
1
Patients with newly diagnosed glioblastoma multiforme.
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Drug: Temozolomide
Administration of temozolomide based on the product labeling.
Radiation: Radiotherapy
Radiotherapy given concomitantly with temozolomide for newly diagnosed glioblastoma multiforme.
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2
Patients with malignant glioma, such as glioblastoma multiforme or anaplastic astrocytoma, showing recurrence or progression after standard therapy.
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Drug: Temozolomide
Administration of temozolomide based on the product labeling.
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Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Sampling Method: | Probability Sample |
Patients with newly diagnosed glioblastoma multiforme. Patients with malignant glioma, such as glioblastoma multiforme or anaplastic astrocytoma, showing recurrence or progression after standard therapy.
Inclusion Criteria:
Patients who are prescribed with temozolomide by local labeling:
Exclusion Criteria:
Responsible Party: | Schering-Plough ( Head, Clinical Trials Registry & Results Disclosure Group ) |
Study ID Numbers: | P05557 |
First Received: | July 25, 2008 |
Last Updated: | October 21, 2008 |
ClinicalTrials.gov Identifier: | NCT00723827 |
Health Authority: | South Korea: Institutional Review Board; South Korea: Korea Food and Drug Administration (KFDA) |
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