Overview

On 29 July 2004, orphan designation (EU/3/04/213) was granted by the European Commission to SmithKline Beecham plc, United Kingdom, for mepolizumab for the treatment of hypereosinophilic syndrome.

The sponsorship was transferred to Glaxo Group Limited, United Kingdom, in September 2008.

The sponsorship was transferred to GlaxoSmithKline Trading Services Limited, Ireland, in May 2018.

The sponsor’s address was updated in April 2020. In April 2020, GlaxoSmithKline Trading Services Limited changed name to GlaxoSmithKline (Ireland) Limited.

Please note that this product was withdrawn from the Union Register of orphan medicinal products in October 2020 on request of the Sponsor.

Hypereosinophilic syndrome is a type of leukaemia (chronic eosinophilic leukaemia) for which it is impossible to find the origin of the cancer cells. It is a disease in which cancer cells are found in the blood, the bone marrow and in tissues. The bone marrow is the spongy tissue inside the large bones in the body. Normally, the bone marrow makes cells called “blasts” that mature into several different types of blood cells that have specific functions in the body. These include red cells, white cells and platelets. Red blood cells carry oxygen and other materials to all tissues of the body. White blood cells fight infection. Platelets make the blood clot. When leukaemia develops, the bone marrow produces large numbers of abnormal blood cells. There are several types of leukaemias. In the hypereosinophilic syndrome, blasts that are developing into white blood cells called “eosinophils” are affected. The eosinophils become too numerous and are then found in the bone marrow, blood and in other tissues such as the heart, lungs, nerves and skin. The excess of eosinophils in tissues can cause disturbances in the function and thereby damage the affected organs. The hypereosinophilic syndrome is life-threatening.

At the time of designation, hypereosinophilic syndrome affected approximately 0.15 in 10,000 people in the European Union (EU)*. This is equivalent to a total of around 7,000 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 25), Norway, Iceland and Liechtenstein. This represents a population of 459,700,000 (Eurostat 2004).

No satisfactory methods exist that were authorised at the time of application.

Different substances produced in the body as interleukin 5, interleukin 3 and granulocyte-monocyte colony stimulating factor (GMCSF) regulate eosinophilic cells production. Antibodies are proteins in the body that target specific shapes (receptors) on the surface of foreign bodies, such as bacteria or cancer cells. Mepolizumab is a human protein that is able to recognise and bind to the receptor of interleukin 5, present on the surface of the eosinophilic cells. It is expected that mepolizumab, by binding to the eosinophilic cells, will prohibit interleukin 5 to interact with its receptor. Thereby interleukin 5 will not be able to stimulate the production of eosinophils anymore. This could then lead to a decrease of the number of eosinophils in blood.

At the time of submission of the application for orphan designation, no clinical trials in patients with hypereosinophilic syndrome were initiated.

Mepolizumab was not marketed anywhere worldwide for hypereosinophilic syndrome. Orphan designation of mepolizumab was granted in the United States for treatment of hypereosinophilic syndrome.

In accordance with Regulation (EC) No 141/2000 of 16 December 1999, the COMP adopted a positive opinion on 16 June 2004 recommending the granting of this designation.

  • the seriousness of the condition;
  • the existence of alternative methods of diagnosis, prevention or treatment;
  • either the rarity of the condition (affecting not more than 5 in 10,000 people in the Community) or 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 quality, safety and efficacy is necessary before a product can be granted a marketing authorisation.

EU/3/04/213: Public summary of positive opinion for orphan designation of mepolizumab for the treatment of hypereosinophilic syndrome

AdoptedReference Number: EMEA/COMP/292/04 Rev. 2

English (EN) (195.84 KB - PDF)

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Key facts

Active substance
Mepolizumab
Intended use
Treatment of hypereosinophilic syndrome
Orphan designation status
Withdrawn
EU designation number
EU/3/04/213
Date of designation
Sponsor

GlaxoSmithKline (Ireland) Limited
12 Riverwalk
Citywest Business Campus
Dublin 24
D24 YK11
Ireland
E-mail: customercontactuk@gsk.com

EMA list of opinions on orphan medicinal product designation

EMA publishes information on orphan medicinal product designation adopted by the Committee for Orphan Medicinal Products (COMP) on the IRIS online platform:

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.

EU register of orphan medicines

The list of medicines that have received an orphan designation in the EU is available on the European Commission's website:

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