EU/3/22/2624 - orphan designation for treatment of soft tissue sarcoma

Doxorubicin
OrphanHuman

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Overview

This medicine was designated as an orphan medicine for the treatment of soft tissue sarcoma in the European Union on 21 June 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:

Soft tissue sarcomas are types of cancer that start in soft tissue, such as muscle, nerves, fat or deep skin tissue. This medicine, also known as DPPG2-TSL-DOX, contains the active substance doxorubicin, a chemotherapy medicine that has been in use to treat various cancers, including soft tissue sarcoma, for a long time. In DPPG2-TSL-DOX, doxorubicin is contained in liposomes (tiny bubbles or vesicles made of fat-like particles) that are thermosensitive. This means that at body temperature (37°C), doxorubicin is stored in the liposomes and is not available in the body. Only when the temperature of the part of the body where the tumour is located is increased (so-called regional hyperthermia), the liposomes become leaky and doxorubicin is released into the tumour microcirculation. Inside the blood vessels of the heated tumour, doxorubicin then reaches very high concentrations that push doxorubicin into the tumour tissue, where doxorubicin then kills the tumour cells.

Based on description provided by sponsor

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

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

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:

Key facts

Active substance
Doxorubicin
Intended use
Treatment of soft tissue sarcoma
Orphan designation status
Positive
EU designation number
EU/3/22/2624
Date of designation
Sponsor

Thermosome GmbH
Am Klopferspitz 19
Martinsried
82152 Planegg
Bavaria
Germany
Email: info@thermosome.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:

  • European Organisation for Rare Diseases (EURORDIS), a non-governmental alliance of patient organisations and individuals active in the field of rare diseases.

  • Orphanet, a database containing information on rare diseases, which includes a directory of patients’ organisations registered in Europe.

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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