On 24 October 2003, orphan designation (EU/3/03/172) was granted by the European Commission to Univar Limited, United Kingdom, for trientine dihydrochloride for the treatment of Wilson’s disease.
The sponsorship was transferred to Univar BV, The Netherlands, in July 2013.
For a list of the administrative updates to this public summary of opinion please refer to the PDF document below.
- What is Wilson’s disease?
Wilson's disease is a genetic disorder that causes excessive copper accumulation in the liver or brain. The liver of a person who has Wilson's disease does not release copper into the bile, as it should. Bile is a liquid produced by the liver that helps with digestion. In Wilson disease, the copper absorbed from the food by the intestines builds up in the liver and injures liver tissue. Eventually, the damage causes the liver to release the copper directly into the bloodstream, which carries the copper throughout the body. The copper accumulated and transported by the bloodstream can then cause damage in other organs like the kidneys, brain, and eyes. If not treated, Wilson's disease can be chronically debilitating and life threatening.
- What is the estimated number of patients affected by the condition?
At the time of designation, Wilson’s disease affected approximately 0.6 in 10,000 people in the European Union (EU)*. This is equivalent to a total of around 23,000 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 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. At the time of designation, this represented a population of 382,800,000 (Eurostat 2003).
- What treatments are available?
Treatment of Wilson's disease generally consists of anti-copper agents to remove excess copper from the body and to prevent it from re-accumulating. Several medicinal products were authorised for Wilson’s disease in the Community at the time of submission of the application for orphan drug designation.
Trientine dihydrochloride could be of potential significant benefit for the treatment of Wilson's disease, by making it available over the whole Community. In addition, trientine dihydrochloride may have a different safety profile for the treatment of the condition from that of medicinal products authorised today. This assumption will have to be confirmed at the time of marketing authorisation. This will be necessary to maintain the orphan status.
- How is this medicine expected to work?
Trientine dihydrochloride binds to the free copper in blood and increases copper excretion in the urine. It might also act by blocking intestinal copper absorption, but this possible mechanism remains to be fully demonstrated.
- What is the stage of development of this medicine?
The active substance, trientine dihydrochloride is authorised in the United Kingdom, in Wilson’s patients who are intolerant of penicillamine therapy. The product authorised in the United Kingdom is exported to Germany, France, Greece, Norway, Switzerland, Austria and Ireland, however supply is restricted to named patients only.
Trientine dihydrochloride has been granted marketing authorisation in the United States for treatment of Wilson’s disease in patients who are intolerant of penicillamine.
In accordance with Regulation (EC) No 141/2000 of 16 December 1999, the COMP adopted a positive opinion on 10 September 2003 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 European Union) 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/3/03/172: Public summary of positive opinion for orphan designation of trientine dihydrochloride for the treatement of Wilson's disease||(English only)||26/04/2004||23/09/2013|
|Active substance||Trientine dihydrochloride|
|Disease/condition||Treatment of Wilson's disease|
|Date of decision||24/10/2003|
|Orphan decision number||EU/3/03/172|
Review of designation
Sponsor’s contact details
3011 GB Rotterdam
Tel. +31 10 275 7840
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.