Data from EMA (European Medicines Agency) - Curated by Marshall Pearce - Last updated 09 August 2017

Indication(s)

Temozolomide Teva is indicated for the treatment of:
- adult patients with newly-diagnosed glioblastoma multiforme concomitantly with radiotherapy (RT) and subsequently as monotherapy treatment.
- children from the age of three years, adolescents and adult patients with malignant glioma, such as glioblastoma multiforme or anaplastic astrocytoma, showing recurrence or progression after standard therapy.

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Category Value
Agency product number EMEA/H/C/001126
Orphan designation No
Date First Approved 28-01-2010
Type Medicinal product subject to restricted medical prescription
Marketing authorisation holder Teva B.V.