On 15 May 2009, orphan designation (EU/3/09/635) was granted by the European Commission to United Therapeutics Europe Ltd, United Kingdom, for treprostinil diethanolamine for the treatment of systemic sclerosis.
- What is systemic sclerosis?
Systemic sclerosis is a complex disease in which the immune system (the body’s natural defences) is overactivated, causing inflammation and overproduction of various proteins, particularly collagen. The reason why the immune system is activated is not known. Collagen is an important component of connective tissue (the tissue that supports the skin and internal organs).
The overproduction of collagen leads to abnormal growth of connective tissue, causing the skin to become thick and hard. It also damages the tissues around the blood vessels of the internal organs, such as the heart, lungs and kidneys. This makes it more difficult for the blood to move through the vessels, causing tissue damage, circulation problems and high blood pressure. The high collagen levels can also stimulate the body’s immune system to attack the collagen, increasing the inflammation in the body.
Systemic sclerosis is a debilitating disease that is long lasting and may be life threatening because of its effects on the heart, lungs and kidneys.
- What is the estimated number of patients affected by the condition?
At the time of designation, systemic sclerosis affected between 1 and 3.5 in 10,000 people in the European Union (EU)*. This is equivalent to a total of between 50,000 and 180,000 people, and is below the threshold for orphan designation, which is 5 people in 10,000. This is based on the information provided by the sponsor and knowledge of the Committee for Orphan Medicinal Products (COMP).
*Disclaimer: For the purpose of the designation, the number of patients affected by the condition is estimated and assessed on the basis of data from the European Union (EU 27), Norway, Iceland and Liechtenstein. This represents a population of 504,800,000 (Eurostat 2009).
- What treatments are available?
At the time of designation, there were no treatments for systemic sclerosis that could stop the build-up of collagen. Treatments authorised in the EU were aimed at relieving the symptoms of the disease and limiting the damage it causes. Several medicines were used to reduce inflammation and circulation problems.
The sponsor has provided sufficient information to show that treprostinil diethanolamine might be of significant benefit for patients with systemic sclerosis mainly because the medicine is expected to be given to patients as tablets. This may contribute to the care of patients because it may allow the medicine to be given less often and may result in the levels of the medicine in the body being more stable over time. This medicine might also have improved safety and effectiveness compared with other treatments. These assumptions will need to be confirmed at the time of marketing authorisation, in order to maintain the orphan status.
- How is this medicine expected to work?
Treprostinil is already available as a solution for continuous infusion under the skin in some countries in the EU. Treprostinil is a substance that it is very similar to prostacyclin, a naturally occurring substance that causes blood vessels to dilate (widen). In systemic sclerosis, treprostinil is expected to act in the same way as prostacyclin to lower the blood pressure in the internal organs and improve the circulation problems.
Treprostinil diethanolamine is a new salt of treprostinil that is expected to be given to patients as sustained-release tablets (tablets that release treprostinil continuously over a few hours).
- What is the stage of development of this medicine?
The effects of treprostinil diethanolamine have been evaluated in experimental models.
At the time of submission of the application for orphan designation, no clinical trials in patients with systemic sclerosis had been started.
At the time of submission, treprostinil diethanolamine was not authorised anywhere in the EU for systemic sclerosis or designated as orphan medicinal product elsewhere for this condition.
In accordance with Regulation (EC) No 141/2000 of 16 December 1999, the COMP adopted a positive opinion on 2 April 2009 recommending the granting of this designation.
- Opinions on orphan medicinal product designations are based on the following three criteria:
- the seriousness of the condition;
- the existence of alternative methods of diagnosis, prevention or treatment;
- and either the rarity of the condition (affecting not more than five in 10,000 people in the Community) or the insufficient returns on investment.
Designated orphan medicinal products are products that are still under investigation and are considered for orphan designation on the basis of potential activity. An orphan designation is not a marketing authorisation. As a consequence, demonstration of the quality, safety and efficacy is necessary before a product can be granted a marketing authorisation.
|Name||Language||First published||Last updated|
|EU/3/09/635: Public summary of positive opinion for orphan designation of treprostinil diethanolamine for the treatment of systemic sclerosis||(English only)||09/06/2009|
|Active substance||Treprostinil diethanolamine|
|Disease/condition||Treatment of systemic sclerosis|
|Date of decision||15/05/2009|
|Orphan decision number||EU/3/09/635|
Review of designation
Sponsor’s contact details:
United Therapeutics Europe Ltd
Unither House Curfew Bell Road Chertsey KT16 9FG
Telephone: +44 1932 573 800
Telefax: +44 1932 571 110
Patient associations’ contact points:
Sklerodermie Selbsthilfe e.V.
Am Wollhaus 2
Telephone: +49 7131 3902425
Telefax: +49 7131 3902426
Association des Sclérodermiques de France
41 Rue du Pont de Fer
Telephone: +33 0820 620 615
Raynaud's & Scleroderma Association (RSA)
112 Crewe Road
Cheshire ST7 2JA
Telephone: +44 1270 872776
Freephone: +44 800 9172494 (for UK enquiries only)
Fax: +44 1270 883556