EU/3/14/1272 - orphan designation for treatment of epidermolysis bullosa

recombinant human alpha 1 chain homotrimer of type VII collagen

Overview

On 4 June 2014, orphan designation (EU/3/14/1272) was granted by the European Commission to Shire Pharmaceuticals (Ireland) Limited, Ireland, for recombinant human alpha 1 chain homotrimer of type VII collagen for the treatment of epidermolysis bullosa.

The sponsorship was transferred to Voisin Consulting S.A.R.L., France, in January 2018.

In October 2021, Voisin Consulting S.A.R.L. changed name to Voisin Consulting Life Sciences.

What is epidermolysis bullosa?

Epidermolysis bullosa describes a group of diseases of the skin, in which the skin is very fragile and forms severe blisters upon minor mechanical friction or injury. The condition is usually present from birth, although some forms occur in adults. The diseases are caused by abnormalities in the genes responsible for the production of certain proteins that make the skin strong and elastic, such as collagen or keratins.

Epidermolysis bullosa is a long-term debilitating and life-threatening condition because the severe blistering and associated scarring and deformities result in poor quality of life and may also reduce life expectancy.

What is the estimated number of patients affected by the condition?

At the time of designation, epidermolysis bullosa affected not more than 0.8 in 10,000 people in the European Union (EU). This was equivalent to a total of not more than 41,000 people*, and is below the ceiling for orphan designation, which is 5 people in 10,000. This isbased on the information provided by the sponsor and the knowledge of the Committee for Orphan Medicinal Products (COMP).

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*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 28), Norway, Iceland and Liechtenstein. This represents a population of 511,100,000 (Eurostat 2014).

What treatments are available?

At the time of designation, no satisfactory methods were authorised in the EU to treat epidermolysis bullosa. A high standard of personal hygiene and wound care were recommended to help blisters heal, to avoid infections and to protect the skin from damage. Painkillers and antibiotics were also used to manage pain and infections. Surgery was sometimes necessary if there were complications such as deformed hands or the development of skin cancer.

How is this medicine expected to work?

In patients with a type of epidermolysis bullosa known as dystrophic epidermolysis bullosa, the blistering is caused by a faulty gene for a protein known as collagen VII that is needed to hold different skin layers together.

This medicine contains functional collagen VII that is lacking in patients with dystrophic epidermolysis bullosa. The medicine is to be given by injection and it is expected that the collagen will be incorporated into the skin, where they will help to hold the skin layers together and prevent the formation of blisters.

The collagen VII in the medicine is made by a method known as 'recombinant DNA technology': it is made by cells into which a gene (DNA) has been introduced that makes them able to produce the protein.

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 the medicine in experimental models was ongoing.

At the time of submission, no clinical trials with the medicine in patients with epidermolysis bullosa had been started.

At the time of submission, the medicine was not authorised anywhere in the EU for epidermolysis bullosa. Orphan designation has been granted in the United States for this condition.

In accordance with Regulation (EC) No 141/2000 of 16 December 1999, the COMP adopted a positive opinion on 9 April 2014 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.

EU/3/14/1272: Public summary of opinion on orphan designation of recombinant human alpha 1 chain homotrimer of type VII collagen for the treatment of epidermolysis bullosa

AdoptedReference Number: EMA/COMP/258960/2014

Key facts

• Active substance:
  recombinant human alpha 1 chain homotrimer of type VII collagen
• Intended use:
  Treatment of epidermolysis bullosa
• Orphan designation status:
  Positive
• EU designation number:
  EU/3/14/1272
• Date of designation:
  04/06/2014
• Sponsor:

  Voisin Consulting Life Sciences ;