EU/3/14/1356 - orphan designation for treatment of acute myeloid leukaemia

Donor T lymphocytes depleted ex-vivo of host alloreactive T cells using photodynamic treatment

Overview

On 19 November 2014, orphan designation (EU/3/14/1356) was granted by the European Commission to Kiadis Pharma Netherlands B.V., the Netherlands, for donor T lymphocytes depleted ex-vivo of host alloreactive T cells using photodynamic treatment for the treatment of acute myeloid leukaemia.

Please note that this product was withdrawn from the Union Register of orphan medicinal products in February 2022 on request of the Sponsor.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

Acute myeloid leukaemia (AML) is a cancer of the white blood cells (cells that fight against infections). In patients with AML, the bone marrow (the spongy tissue inside the large bones, where blood cells are produced) produces large numbers of abnormal, immature white blood cells. These abnormal cells quickly build up in large numbers in the bone marrow and are found in the blood.

AML is a long-term debilitating and life-threatening disease because these abnormal immature cells take the place of the normal blood cells, causing bleeding episodes, blood clots and reducing the patient's ability to fight infections.

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

At the time of designation, AML affected approximately 1 in 10,000 people in the European Union (EU). This was equivalent to a total of 51,000 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?

Treatment for AML is complex and depends on a number of factors including the extent of the disease, whether it has been treated before, and the patient's age, symptoms and general state of health. At the time of designation, the main treatments for AML were chemotherapy (medicines to treat cancer) and haematopoietic (blood) stem-cell transplantation (a complex procedure where the patient receives stem cells from a donor to help restore the bone marrow with healthy cells). However, a risk of this procedure is graft-versus-host disease, a potentially fatal complication in which the transplanted cells recognise the patient's cells as 'foreign' and attack them.

The sponsor has provided sufficient information to show that this medicine might be of significant benefit for patients with AML because early studies suggest that it might help rebuild the patient's immune system following a stem-cell transplant and may also help to fight the leukaemia cells. 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?

For many patients with AML who require haematopoietic stem-cell transplantation, it is often difficult to find a fully matched donor, which is important to reduce the risk of the transplanted cells attacking the patient's own cells.

This medicine is made of T cells, a type of white blood cell, extracted from a donor who is partly matched to the patient (e.g. a close relative). Before being injected into the patient, a specific group of T cells (known as alloreactive T cells) that is known to attack the patient's cells is first removed. The remaining T cells are then injected into the patient after the patient has received a haematopoietic stem-cell transplant depleted of T cells from the same partly matched donor. The injected T cells are expected to help early recovery of the patient's immune system without attacking the patient's own cells, and to help fight against the leukaemia cells.

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 AML were ongoing.

At the time of submission, the medicine was not authorised anywhere in the EU for AML 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 9 October 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.

Key facts

• Active substance:
  Donor T lymphocytes depleted ex-vivo of host alloreactive T cells using photodynamic treatment
• Intended use:
  Treatment of acute myeloid leukaemia
• Orphan designation status:
  Withdrawn
• EU designation number:
  EU/3/14/1356
• Date of designation:
  19/11/2014
• Sponsor:

  Kiadis Pharma Netherlands B.V; Entrada 231-234; 1114 AA Amsterdam-Duivendrecht; The Netherlands; Tel. [phone]; Fax [phone]; E-mail: [e-mail]

Review of designation

The Committee for Orphan Medicinal Products reviews the orphan designation of a product if it is approved for marketing authorisation.