EU/3/22/2726 - orphan designation for treatment of autosomal dominant polycystic kidney disease

Mebendazole

Overview

This medicine was designated as an orphan medicine for the treatment of autosomal dominant polycystic kidney disease in the European Union on 9 December 2022.

This means that the developer will receive scientific and regulatory support from EMA to advance their medicine to the stage where they can apply for a marketing authorisation.

Orphan designation does not mean the medicine is available or authorised for use. All medicines, including designated orphan medicines, must be authorised before they can be marketed and made available to patients in the EU.

During the medicine's development, doctors may be able to enrol patients in clinical trials investigating the medicine. For information on ongoing clinical trials in the EU, see:

• EU Clinical Trials Register

• ClinicalTrials.gov

How the medicine is expected to work

Autosomal dominant polycystic kidney disease (ADPKD) is an inherited disorder caused by mutations in the PDK1 and PDK2 genes. These mutations result in the proliferation of a certain type of kidney cells and their excessive secretion of fluid, leading to the development of cysts (fluid-filled sacs) in the kidneys and associated loss of kidney function.

Mebendazole is currently used as an antiparasitic agent in humans and animals. Its acts by binding to tubulin, a protein involved in key cellular processes, of parasites, leading to their paralysis and death. Mebendazole is also thought to prevent the division of rapidly dividing cells and is therefore expected to prevent the formation of cysts in kidneys of patients with ADPKD.

Based on description provided by sponsor

Stage of development at time of orphan designation

At the time of submission of the application for orphan designation:

• The effects of the medicine had been evaluated in experimental models.
• No clinical trials with the medicine in patients with autosomal dominant polycystic kidney disease had been started.  

More information on how potential new medicines are tested during their development is available on Authorisation of medicines.

About orphan designation

Medicines intended for rare diseases can be granted an orphan designation during their development.

The orphan designation allows the developer to benefit from:

• scientific and regulatory support to advance their medicine to the stage where they can request marketing authorisation;

• market exclusivity once the medicine is on the market.

To qualify for orphan designation, a medicine must meet a number of criteria:

• it must be intended for the treatment, prevention or diagnosis of a disease that is life-threatening or chronically debilitating;

• the prevalence of the condition in the EU must not be more than 5 in 10,000 or it must be unlikely that marketing of the medicine would generate sufficient returns to justify the investment needed for its development;

• there are no satisfactory alternative methods for the diagnosis, prevention or treatment of the condition or, if such a method exists, the medicine is of significant benefit to those affected by the condition.

EMA's Committee for Orphan Medicinal Products (COMP) is responsible for issuing opinions on applications for orphan designations.

The Agency sends the COMP opinion to the European Commission, which is responsible for granting the orphan designation. The full list of orphan designations is available in the Community register of orphan medicinal products for human use.

For more information, see:

• Orphan designation: Overview

• Rare diseases, orphan medicines - Getting the facts straight

Minutes of the COMP meeting 8-10 November 2022

Adopted Reference Number: EMA/COMP/897858/2022 Rev.1

Key facts

• Active substance:
  Mebendazole
• Intended use:
  Treatment of autosomal dominant polycystic kidney disease
• Orphan designation status:
  Positive
• EU designation number:
  EU/3/22/2726
• Date of designation:
  09/12/2022
• Sponsor:

  Healx Technology Limited; Clifton House; Fitzwilliam Street Lower; Dublin 2 D02 XT91; Ireland; E-mail: [e-mail]