EU/3/05/305

Table of contents

About

Please note that this product was withdrawn from the Community Register of designated orphan medicinal products in April 2012 on request of the sponsor.

On 26 August 2005 orphan designation (EU/3/05/305) was granted by the European Commission to Novartis Europharm Limited, United Kingdom, for imatinib mesilate for the treatment of dermatofibrosarcoma protuberans.

Imatinib mesilate for treatment of dermatofibrosarcoma protuberans has been authorised in the EU as Glivec since 13 September 2006.

Key facts

Active substance
imatinib mesilate
Medicine name
Glivec
Disease / condition
Treatment of dermatofibrosarcoma protuberans
Date of first decision
26/08/2005
Outcome
Expired
EU designation number
EU/3/05/305

Sponsor's contact details

Novartis Europharm Limited
Frimley Business Park
Camberley GU16 7SR
United Kingdom
Tel. +41 61 324 11 11 (Switzerland)
E-mail: orphan.enquiries@novartis.com

Patients' organisations

For contact details of patients’ organisations whose activities are targeted at rare diseases, see:

  • European Organisation for Rare Diseases (EURORDIS), a non-governmental alliance of patient organisations and individuals active in the field of rare diseases.
  • Orphanet, a database containing information on rare diseases, which includes a directory of patients’ organisations registered in Europe;

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