EU/3/22/2579 - orphan designation for treatment of Dravet syndrome

18‐mer antisense oligonucleotide complementary to SCN1A mRNA

sodium salt

Overview

This medicine was designated as an orphan medicine for the treatment of Dravet syndrome in the European Union on 24 February 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

This medicine, also known as STK-001, is an oligonucleotide. Oligonucleotides are short sequences of acid substances called nucleic acids. They are similar to those that carry the genetic information in the cells. The genetic information is used to produce proteins. Oligonucleotides can be used to block a cell from producing a protein. In the case of Dravet syndrome, the oligonucleotide aims to increase the production of a protein called SCN1A. This protein is a critical element in the nervous function of the body, and is lacking in patients with Dravet syndrome. By increasing the production of SCN1A, the medicine is expected to improve the symptoms of the condition.

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.
• Clinical trials with the medicine in patients with Dravet syndrome were ongoing.

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 on 18-20 January 2022

Adopted Reference Number: EMA/COMP/63104/2022

Key facts

• Active substance:
  • 18‐mer antisense oligonucleotide complementary to SCN1A mRNA
  • sodium salt
• Intended use:
  Treatment of Dravet syndrome
• Orphan designation status:
  Positive
• EU designation number:
  EU/3/22/2579
• Date of designation:
  24/02/2022
• Sponsor:

  Pharma Gateway AB;