EU/3/16/1792 - orphan designation for treatment of diffuse large B-cell lymphoma

Valproic acid
OrphanHuman

Overview

On 18 November 2016, orphan designation (EU/3/16/1792) was granted by the European Commission to Valcuria AB, Sweden, for valproic acid for the treatment of diffuse large B-cell lymphoma.

Diffuse large B-cell lymphoma is a type of blood cancer and the most common form of a group of blood cancers known as non-Hodgkin lymphomas.

Diffuse large B-cell lymphoma affects a type of white blood cell called B lymphocytes, or B cells. In patients with this cancer, the B cells multiply too quickly and live for too long, so there are too many of them in the lymph nodes. The first sign of the disease is usually a lump in the neck, under the arm or in the groin area, which is caused by an enlarged lymph node. Patients with diffuse large B-cell lymphoma may also have fever, tiredness, night sweats or weight loss that have no obvious cause.

Although some people with diffuse large B-cell lymphoma can be cured, it remains a serious and life-threatening disease, particularly when the disease is diagnosed late or has come back after treatment.

At the time of designation, diffuse large B-cell lymphoma affected approximately 4.3 in 10,000 people in the European Union (EU). This was equivalent to a total of around 221,000 people1, 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)


1Disclaimer: 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).

At the time of designation, several medicines were authorised for the treatment of diffuse large B-cell lymphoma in the EU. The main treatment was chemotherapy (medicines to treat cancer) usually in combination with medicines called monoclonal antibodies and sometimes with radiotherapy (treatment with radiation). Autologous haematopoietic (blood) stem-cell transplantation was also used in patients at risk of the disease coming back after treatment. This is a procedure where the patient's bone marrow is replaced with the patient's own stem cells to form new bone marrow that produces healthy blood cells.

The sponsor has provided sufficient information to show that this medicine might be of significant benefit for patients with diffuse large B-cell lymphoma. This is based on preliminary results in patients showing that the medicine can be added to standard treatment and may prolong survival. This assumption will need to be confirmed at the time of marketing authorisation, in order to maintain the orphan status.

Valproic acid (or valproate) is a well-known medicine used in the EU to treat epilepsy and bipolar disorder. In diffuse large B-cell lymphoma, the medicine is expected to work by blocking the activity of histone deacetylases (HDACs), proteins that promote cell division. By blocking HDACs, the medicine is expected to stop the cancer cells from dividing and multiplying, leading to cell death. Valproic acid is also thought to increase the sensitivity of the cancer cells to standard cancer treatments, for example by increasing production of CD20 receptors, which are the target of the cancer medicine rituximab. This increases the effectiveness of rituximab treatment, helping to control the cancer and improve survival.

The effects of the 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 diffuse large B-cell lymphoma were ongoing.

At the time of submission, the medicine was not authorised anywhere in the EU for diffuse large B-cell lymphoma 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 6 October 2016 recommending the granting of this designation.

  • 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
Valproic acid
Intended use
Treatment of diffuse large B-cell lymphoma
Orphan designation status
Positive
EU designation number
EU/3/16/1792
Date of designation
Sponsor

Valcuria AB
Scheelevägen 2
223 81 Lund
Sweden
Tel. +46 709 22 41 40
E-mail: info@respiratorius.com

EMA list of opinions on orphan medicinal product designation

EMA publishes information on orphan medicinal product designation adopted by the Committee for Orphan Medicinal Products (COMP) on the IRIS online platform:

Patients' organisations

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.

EU register of orphan medicines

The list of medicines that have received an orphan designation in the EU is available on the European Commission's website:

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