EU/3/14/1302 - orphan designation for treatment of Prader-Willi syndrome
Oxytocin
OrphanHuman
Overview
On 29 July 2014, orphan designation (EU/3/14/1302) was granted by the European Commission to Maïté Tauber, France, for oxytocin for the treatment of Prader-Willi syndrome.
The sponsorship was transferred to OT4B, France in January 2021.
Prader-Willi syndrome is a genetic condition caused by defects in specific areas of chromosome 15. This causes a wide range of symptoms, some of which can appear at birth, such as feeding problems, small size and reduced muscle strength. During childhood further symptoms develop, including absence of the sense of satiety often leading to severe obesity, short stature, incomplete sexual development, learning difficulties and behavioural problems, such as aggression and stubbornness.
Prader-Willi syndrome is a life-long debilitating and life-threatening disease because of its serious symptoms, particularly learning difficulties, behavioural problems and obesity.
At the time of designation, Prader-Willi syndrome affected approximately 2 in 10,000 people in the European Union (EU). This was equivalent to a total of around 102,000 people*, and is below the ceiling for orphan designation, which is 5 people in 10,000. This isbased on the information provided by the sponsor and the knowledge of the Committee for Orphan Medicinal Products (COMP).
*Disclaimer: For the purpose of the designation, the number of patients affected by the condition is estimated and assessed on the basis of data from the European Union (EU 28), Norway, Iceland and Liechtenstein. This represents a population of 511,100,000 (Eurostat 2014).
At the time of designation, growth hormone was authorised in the EU for treating Prader-Willi syndrome. In addition, patients' symptoms were treated or managed in various ways, including supervised access to food to prevent obesity.
The sponsor has provided sufficient information to show that oxytocin might be of significant benefit for patients with Prader-Willi syndrome because early studies show improvements in the behaviour and feeding patterns of patients with the condition. This assumption will need to be confirmed at the time of marketing authorisation, in order to maintain the orphan status.
Oxytocin is a hormone mostly associated with childbirth because of its effect in uterine (womb) contractions. Oxytocin is also thought to influence several aspects of behaviour (such as bonding with other people) and to regulate food intake. A lower number of oxytocin-producing cells have been reported in the brain of patients with Prader-Willi syndrome. The medicine is to be used to increase the patients' levels of oxytocin and thereby improve behaviour and feeding in patients with Prader-Willi.
The effects of oxytocin have been evaluated in experimental models.
At the time of submission of the application for orphan designation, clinical trials with oxytocin in patients with Prader-Willi syndrome were ongoing.
At the time of submission, oxytocin was not authorised anywhere in the EU for Prader-Willi syndrome or designated as an orphan medicinal product elsewhere for this condition.
In accordance with Regulation (EC) No 141/2000 of 16 December 1999, the COMP adopted a positive opinion on 12 June 2014 recommending the granting of this designation.
- the seriousness of the condition;
- the existence of alternative methods of diagnosis, prevention or treatment;
- either the rarity of the condition (affecting not more than 5 in 10,000 people in the EU) or insufficient returns on investment.
Designated orphan medicinal products are products that are still under investigation and are considered for orphan designation on the basis of potential activity. An orphan designation is not a marketing authorisation. As a consequence, demonstration of quality, safety and efficacy is necessary before a product can be granted a marketing authorisation.
Key facts
- Active substance
- Oxytocin
- Intended use
- Treatment of Prader-Willi syndrome
- Orphan designation status
- Positive
- EU designation number
- EU/3/14/1302
- Date of designation
- Sponsor
OT4B
109 Avenue de Lespinet
31400 Toulouse
France
Email: cbastos@ot4b.com
Review of designation
The Committee for Orphan Medicinal Products reviews the orphan designation of a product if it is approved for marketing authorisation.
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: