EU/3/16/1762 - orphan designation for treatment of paroxysmal nocturnal haemoglobinuria

synthetic 15-amino-acid macrocyclic peptide acylated with a polyethyleneglycol palmitoylated linker (zilucoplan)

Overview

This medicine is now known as zilucoplan.

On 14 October 2016, orphan designation (EU/3/16/1762) was granted by the European Commission to Ra Europe Limited, United Kingdom, for synthetic 15-amino-acid macrocyclic peptide acylated with a polyethyleneglycol palmitoylated linker for the treatment of paroxysmal nocturnal haemoglobinuria.

The sponsorship was transferred to Pharma Gateway AB, Sweden, in September 2018 and subsequently, to UCB Pharma, Belgium, in November 2020.

Please note that this product was withdrawn from the Union Register of orphan medicinal products in February 2022 on request of the Sponsor.

What is paroxysmal nocturnal haemoglobinuria?

Paroxysmal nocturnal haemoglobinuria (PNH) is a condition in which there is excessive breakdown of red blood cells, leading to the release into the urine of a large amount of haemoglobin (the pigment contained in the cells). Because of the red colour of haemoglobin, the passing of red urine, particularly in the mornings, is usually the most obvious sign of the disease. Patients may also experience problems related to blood clotting.

The condition is caused by the lack of certain proteins on the surface of the red blood cells which normally protect them from being destroyed by the immune system (the body's natural defences).

PNH is a long-term debilitating and life-threatening condition due to its complications including abdominal pain, infection and kidney problems, and problems due to bleeding and blood clots.

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

At the time of designation, PNH affected less than 0.2 in 10,000 people in the European Union (EU). This was equivalent to a total of fewer than 10,000 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).

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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 513,700,000 (Eurostat 2016).

What treatments are available?

At the time of designation, the medicine Soliris (eculizumab) was authorised in the EU for the treatment of PNH. Bone marrow transplantation to replace the defective red blood cells was another therapy available to patients, however this treatment is available to only a small proportion of patients since a suitable donor is required. Other methods such as blood transfusions and treatment with blood-thinning compounds to prevent clotting were used in some patients to improve symptoms.

The sponsor has provided sufficient information to show that the medicine might be of significant benefit for patients with PNH because preliminary data suggest that it can be used in patients for whom Soliris does not work. In addition, patients may be able to take the medicine themselves, as it would be injected under the skin and not into a vein. 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?

This medicine is expected to work by attaching to and blocking the C5 complement protein, one of the proteins of the 'complement system', which is part of the body's defence system. In patients with PNH, the complement system causes damage to the patients' own blood cells which lack proteins on their surface that would normally protect them. By blocking the C5 complement protein, this medicine is expected to prevent the complement system from damaging the blood cells, thereby helping to relieve the symptoms of the disease.

What is the stage of development of this medicine?

The effects of this medicine have been evaluated in experimental models.

At the time of submission of the application for orphan designation, clinical trials with the medicine in patients with PNH were planned.

At the time of submission, the medicine was not authorised anywhere in the EU for PNH 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 8 September 2016 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/3/16/1762: Public summary of positive opinion for orphan designation of synthetic 15-amino-acid macrocyclic peptide acylated with a polyethyleneglycol palmitoylated linker for the treatment of paroxysmal nocturnal hae...

Adopted Reference Number: EMA/620104/2016

Key facts

• Active substance:
  synthetic 15-amino-acid macrocyclic peptide acylated with a polyethyleneglycol palmitoylated linker (zilucoplan)
• Intended use:
  Treatment of paroxysmal nocturnal haemoglobinuria
• Orphan designation status:
  Withdrawn
• EU designation number:
  EU/3/16/1762
• Date of designation:
  14/10/2016
• Sponsor:

  UCB Pharma;