EU/3/02/113 - orphan designation for treatment of adrenal cortical carcinoma
mitotane
OrphanHuman
Please note that this product was withdrawn from the Community Register of designated Orphan Medicinal Products in May 2005 on request from the sponsor.
On 11 September 2002, orphan designation (EU/3/02/113) was granted by the European Commission to Etablissement Pharmaceutique des Hôpitaux de Paris (AGEPS-EPHP), France, for mitotane for the treatment of adrenal cortical carcinoma.
Cancer of the adrenal cortex is a disease in which cancer (malignant) cells are found in the adrenal cortex, which is the outside layer of the adrenal gland. Cancer of the adrenal cortex is also called adrenal cortical carcinoma. There are two adrenal glands, one above each kidney in the back of the upper abdomen. The adrenal cortex produces steroid hormones. Steroid hormones include sex hormones and hormones used to control minerals and sugar in the body. Cancer cells in the adrenal cortex may make too much of one or more hormones, which can cause symptoms such as high blood pressure, weakening of the bones, or diabetes. If male or female hormones are affected, the body may go through changes such as a deepening of the voice, growing hair on the face, swelling of the sex organs, or swelling of the breasts. Cancers that make hormones are called functioning tumours. Many cancers of the adrenal cortex do not make extra hormones and are called non-functioning tumours. Adrenal cortical carcinoma is a life-threatening condition, mainly due to frequent spreading of the cancer cells (metastasis).
The methods of treatment used include surgery, chemotherapy (using drugs to kill the cancer cells) and radiotherapy (using x-rays or other high-energy rays to kill cancer cells). An anticancer medicinal product had been authorised for the treatment of the symptoms of the condition in the Community at the time of the submission of the application for orphan designation. However, there is no authorised treatment available to target adrenocortical carcinoma.
According to the information provided by the sponsor, adrenocortical carcinoma was considered to affect about 4,000 people in the European Union.
*Disclaimer: The number of patients affected by the condition is estimated and assessed for the purpose of the designation, for a European Community population of 377,000,000 (Eurostat 2001) and may differ from the true number of patients affected by the condition. This estimate is based on available information and calculations presented by the sponsor at the time of the application.
The potential of mitotane to be toxic to the adrenal cells, and therefore to limit tumour growth has been known since several decades but the exact mechanism of action is not known. Mitotane may be of potential interest for the treatment of adrenocortical carcinoma, particularly based on the effect, which have been shown in experimental models of the condition and in several small clinical studies.
At the time of submission of the application for orphan designation, clinical trials in patients with adrenal cortical carcinoma had been completed.
Mitotane had been marketed in the United States of America and Canada for the treatment of the condition at the time of the orphan application. Mitotane had not been designated as orphan medicinal product elsewhere for this condition, at the time of submission.
According to Regulation (EC) No 141/2000 of 16 December 1999, the Committee for Orphan Medicinal Products (COMP) adopted on 18 July 2002 a positive opinion recommending the grant of the above-mentioned designation.
Designated orphan medicinal products are still investigational products, which have been considered for designation on the basis of potential activity. An orphan designation is not a marketing authorisation. As a consequence, demonstration of the quality, safety and efficacy will be necessary before this product can be granted a marketing authorisation.
Etablissement Pharmaceutique des Hôpitaux de Paris (AGEPS-EPHP)
7, rue du Fer à Moulin
F-75221 Paris CEDEX 5
France
Telephone: +33 1 46 69 15 90
Telefax: +33 1 46 69 14 20
E-mail: francois.guyon@eps.ap-hop-paris.fr
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:
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.
The list of medicines that have received an orphan designation in the EU is available on the European Commission's website: