EU/3/08/559

Table of contents

About

Please note that this product was withdrawn from the Community register of designated orphan medicinal products in April 2014 on request of the sponsor.

On 5 September 2008, orphan designation (EU/3/08/559) was granted by the European Commission to Actelion Registration Limited, United Kingdom, for bosentan for the treatment of idiopathic pulmonary fibrosis.

For a list of the administrative updates to this public summary of opinion please refer to the PDF document below.

Key facts

Active substance
Bosentan
Disease / condition
Treatment of idiopathic pulmonary fibrosis
Date of first decision
05/09/2008
Outcome
Withdrawn
EU designation number
EU/3/08/559

Sponsor's contact details

Actelion Registration Limited
BSI Building 13th floor
389 Chiswick High Road
London W4 4AL
United Kingdom
Tel. + 44 (0)20 8987 3320
Fax + 44 (0)20 8987 3322
E-mail: registration@actelion.com

Patients' organisations

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

  • Orphanet, a database containing information on rare diseases, which includes a directory of patients’ organisations registered in Europe.

  • European Organisation for Rare Diseases (EURORDIS), a non-governmental alliance of patient organisations and individuals active in the field of rare diseases.

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