On 9 December 2011, orphan designation (EU/3/11/936) was granted by the European Commission to Bio Products Laboratory Ltd, United Kingdom, for human haptoglobin for the treatment of sickle cell disease.
- What is sickle cell disease?
Sickle cell disease is a genetic disease in which the red blood cells become rigid and sticky, and change from being disc-shaped to being crescent-shaped (like a sickle). The change in shape is caused by the presence of an abnormal form of haemoglobin, the protein in red blood cells that carries oxygen around the body. In patients with sickle cell disease, the abnormal red blood cells attach to the walls of blood vessels and block them, restricting the flow of nutrients to the internal organs such as the heart, lungs and spleen. Because the abnormal red blood cells have a shorter life span, they release haemoglobin into the blood circulation rather than carrying it to the internal organs where it is needed. This causes severe pain and damage to these organs as well as repeated infections and anaemia (low red blood cell counts).
Sickle cell disease is a severe disease that is long lasting and may be life threatening because of damage to the heart and the lungs, anaemia and infections.
- What is the estimated number of patients affected by the condition?
At the time of designation, sickle cell disease affected approximately 1.5 in 10,000 people in the European Union (EU)*. This is equivalent to a total of around 76,000 people, and is below the ceiling for orphan designation, which is 5 people in 10,000. This is based on the information provided by the sponsor and the 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 506,300,000 (Eurostat 2011).
- What treatments are available?
At the time of designation, the only medicine authorised in the EU to treat sickle cell disease was hydroxyurea (also known as hydroxycarbamide). The main treatment for sickle cell disease was blood transfusion. This was usually combined with ‘iron chelators’, medicines used to reduce the high iron levels in the body caused by repeated blood transfusions, which are necessary in patients with long-term anaemias such as sickle cell disease. In some cases, haematopoietic (blood) stem cell transplantation was used (a complex procedure where the patient receives stem cells from a matched donor to help restore the bone marrow) to allow the patient to produce red blood cells containing normal haemoglobin.
The sponsor has provided sufficient information to show that human haptoglobin might be of significant benefit for patients with sickle cell disease because early studies in experimental models show that it works in a different way to existing medicines and might improve the treatment of patients with this condition. This assumption 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?
Human haptoglobin is a protein obtained from human blood. It works by attaching to free haemoglobin. In sickle cell disease, the medicine is expected to reduce the amount of free haemoglobin that is released into the circulation from the abnormal red blood cells. This is expected to reduce the symptoms of the disease. The haptoglobin-haemoglobin complex is then broken down by specialised cells called macrophages and cleared from the body.
- What is the stage of development of this medicine?
At the time of submission of the application for orphan designation, the evaluation of the effects of human haptoglobin in experimental models was ongoing.
At the time of submission of the application for orphan designation, no clinical trials with human haptoglobin in patients with sickle cell disease had been started.
At the time of submission, human haptoglobin was not authorised anywhere in the EU for treatment for sickle cell disease or designated as an 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 7 October 2011 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;
- either the rarity of the condition (affecting not more than 5 in 10,000 people in the EU) 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.
|Name||Language||First published||Last updated|
|EU/3/11/936: Public summary of opinion on orphan designation: Human haptoglobin for the treatment of sickle cell disease||(English only)||20/12/2011|
|Active substance||Human haptoglobin|
|Disease/condition||Treatment of sickle cell disease|
|Date of decision||09/12/2011|
|Orphan decision number||EU/3/11/936|
Review of designation
The Committee for Orphan Medicinal Products reviews the orphan designation of a product if it is approved for marketing authorisation.
Sponsor’s contact details:
Bio Products Laboratory Ltd
Hertfordshire WD6 3BX
Telephone: +44 20 82 58 22 00
Telefax: +44 20 82 58 26 08
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.