EU/3/10/802 - orphan designation for treatment of idiopathic pulmonary fibrosis
2-(2-chlorophenyl)-4-[3-(dimethylamino)phenyl]-5-methyl-1H-pyrazolo[4,3-C]pyridine-3,6(2H,5H)-dione
OrphanHuman
Overview
On 26 November 2010, orphan designation (EU/3/10/802) was granted by the European Commission to Fulcrum Pharma (Europe) Ltd, United Kingdom, for 2-(2-chlorophenyl)-4-[3-(dimethylamino)phenyl]-5-methyl-1H-pyrazolo[4,3-C]pyridine-3,6(2H,5H)-dione for the treatment of idiopathic pulmonary fibrosis.
The sponsorship was transferred to GenKyoTex Innovation S.A.S, France, in August 2011.
The sponsorship was transferred to GenKyoTex S.A., France in January 2018.
Idiopathic pulmonary fibrosis is a long-term disease of the lungs characterised by the progressive formation of hard tissue in the lining of the lungs. 'Idiopathic' means that the cause of the disease is unknown. As the tissue becomes thicker and forms scars, the lungs become unable to work normally, reducing the transfer of oxygen from the air into the blood. Patients with idiopathic pulmonary fibrosis have a persistent cough, frequent lung infections and severe shortness of breath that worsens over time.
Idiopathic pulmonary fibrosis is a long-term debilitating disease that may be life-threatening because the lungs gradually lose their ability to work properly.
At the time of designation, idiopathic pulmonary fibrosis affected approximately 3 in 10,000 people in the European Union (EU)*. This is equivalent to a total of around 152,000 people, and is below the threshold for orphan designation, which is 5 people in 10,000. This is based 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 27), Norway, Iceland and Liechtenstein. This represents a population of 506,500,000 (Eurostat 2010).
At the time of designation, corticosteroids (anti-inflammatory medicines) were authorised in the EU for the treatment of idiopathic pulmonary fibrosis. Medicines that reduce the activity of the immune system (the body's natural defences) were also used. In some patients, the disease needed to be treated with a lung transplant.
The sponsor has provided sufficient information to show that this medicine might be of significant benefit for patients with idiopathic pulmonary fibrosis because early studies in experimental models show that it works in a different way to existing treatments and might improve the outcome of patients with this condition. This assumption will need to be confirmed at the time of marketing authorisation, in order to maintain the orphan status.
The medicine is expected to work by blocking the action of an enzyme called 'NADPH oxidase 4'. This enzyme is thought to be responsible for the production of toxic molecules containing oxygen, which are involved in causing the lung damage seen in idiopathic pulmonary fibrosis. By blocking the actions of NADPH oxidase 4, the medicine is expected to reduce lung damage, thereby slowing down or reversing the symptoms of the disease.
The effects of the medicine have been evaluated in experimental models.
At the time of submission of the application for orphan designation, no clinical trials with the medicine in patients with idiopathic pulmonary fibrosis had been started.
At the time of submission, the medicine was not authorised anywhere in the EU for idiopathic pulmonary fibrosis. Orphan designation of the medicine had been granted in the United States of America for this condition.
In accordance with Regulation (EC) No 141/2000 of 16 December 1999, the COMP adopted a positive opinion on 9 September 2010 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 European Union) 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
- 2-(2-chlorophenyl)-4-[3-(dimethylamino)phenyl]-5-methyl-1H-pyrazolo[4,3-C]pyridine-3,6(2H,5H)-dione
- Intended use
- Treatment of idiopathic pulmonary fibrosis
- Orphan designation status
- Positive
- EU designation number
- EU/3/10/802
- Date of designation
- Sponsor
Calliditas Therapeutics France S.A.S.
Forum 2
Archamps Technopole
218 Avenue Marie Curie
74166 Saint-Julien-En-Genevois Cedex
FranceE-mail: malin.waage@calliditas.com
Review of designation
The Committee for Orphan Medicinal Products reviews the orphan designation of a product if it is approved for marketing authorisation.
Update history
| Date | Update |
|---|---|
| August 2022 | The sponsor's name was changed from GenKyoTex S.A. to Calliditas Therapeutics France S.A.S in August 2022. |
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: