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Ingetrokken vergunning voor het in de handel brengen - Europa

  • Handelsnaam : IMATINIB TEVA B.V.
  • ATC-code : L01XE01
  • EU-nummer : EU/1/17/1243
  • datum van de VHB: 15/11/2017
  • houder van de VHB: TEVA PHARMACEUTICALS EUROPE B.V.

Therapeutic indication

Imatinib Teva B.V. is indicated for the treatment of:
* Paediatric patients with newly diagnosed Philadelphia chromosome (bcr-abl) positive (Ph+) chronic myeloid leukaemia (CML) for whom bone marrow transplantation is not considered as the first line of treatment.
* Paediatric patients with Ph+ CML in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis.
* Adult patients with Ph+ CML in blast crisis.
* Adult and paediatric patients with newly diagnosed Philadelphia chromosome positive acute lymphoblastic leukaemia (Ph+ ALL) integrated with chemotherapy.
* Adult patients with relapsed or refractory Ph+ ALL as monotherapy.
* Adult patients with myelodysplastic/myeloproliferative diseases (MDS/MPD) associated with platelet-derived growth factor receptor (PDGFR) gene re-arrangements.
* Adult patients with advanced hypereosinophilic syndrome (HES) and/or chronic eosinophilic leukaemia (CEL) with FIP1L1-PDGFRα rearrangement.
The effect of imatinib on the outcome of bone marrow transplantation has not been determined.

Imatinib Teva B.V. is indicated for:
* The treatment of adult patients with Kit (CD 117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumours (GIST).
* The adjuvant treatment of adult patients who are at significant risk of relapse following resection of Kit (CD117)-positive GIST. Patients who have a low or very low risk of recurrence should not receive adjuvant treatment.
* The treatment of adult patients with unresectable dermatofibrosarcoma protuberans (DFSP) and adult patients with recurrent and/or metastatic DFSP who are not eligible for surgery.

De documenten op deze website zijn louter ter informatie. Het materiaal is geenszins bestemd om professionele medische zorgen door een gediplomeerde specialist te vervangen en mag niet worden gebruikt als basis voor een diagnose of behandeling.