EU/3/22/2624 - orphan designation for treatment of soft tissue sarcoma
Doxorubicin
OrphanHuman
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:
To qualify for orphan designation, a medicine must meet a number of criteria:
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:
Thermosome GmbH
Am Klopferspitz 19
Martinsried
82152 Planegg
Bavaria
Germany
Email: info@thermosome.com
EMA publishes information on orphan medicinal product designation adopted by the Committee for Orphan Medicinal Products (COMP) on the IRIS online platform:
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.
The list of medicines that have received an orphan designation in the EU is available on the European Commission's website: