Data from EMA (European Medicines Agency) - Curated by EPG Health - Last updated 16 July 2018

Indication(s)

Temomedac 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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More information

Category Value
Agency product number EMEA/H/C/001124
Orphan designation No
Date First Approved 25-01-2010
Type Medicinal product subject to restricted medical prescription
Marketing authorisation holder medac Gesellschaft für klinische Spezialpräparate mbH