Rare Diseases
AOP Health is committed to helping people with rare diseases. Focusing on the special needs of patients with rare diseases, we investigate, develop and provide these into the market.
What exactly are rare diseases?
Whether a disease is defined as a rare disease depends on the frequency of its occurrence in the population. However, from the global point of view the definition is not consistent.
Thus, in Europe those diseases that occur in less than 5 per 10,000 residents are defined as rare diseases.
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Univ. Prof. Irene Lang, MD
Global figures
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Dr. Rainer Riedl | Chairman of Debra Austria
What are the special features of RARE DISEASES?
Nearly all genetic disorders are rare diseases, but not all rare diseases are caused by genetic factors. Rare diseases include, for instance, some very rare infectious diseases, rare forms of autoimmune disorders, and even rare cancers.
Most causes of rare diseases have not been explained yet.
For many diseases the first symptoms may occur shortly after birth or in early childhood. In around 50% the first symptoms occur in adulthood.
Characteristics of rare diseases
- Around half of the diseases occur in children; nearly all are caused by genetic factors
- Many rare diseases are nearly unknown; very few specialists exist for these
- The pathway to the correct diagnosis is tedious and frequently spans a period of several years
- For the majority of the diseases (more than 95%) there are, to date, no specific therapy options.
Many rare diseases are life-threatening or very burdensome
Specific Difficulties & Problems
Lengthy Process of Diagnosis
Many rare diseases have not been sufficiently investigated so far to permit their unequivocal diagnosis at an early point in time. The time until the establishment of a reliable diagnosis is measured here not in weeks or months; some patients wait for several years. Quite frequently the patients are confronted with a series of false diagnoses due to the incorrect interpretation of their symptoms.
"The time period from the onset of symptoms to the diagnosis may be 5 years or even 10 years for narcolepsy. To my knowledge, the longest period of diagnosis for this condition was 40 years."
"In the case of my daughter who has Epidermolysis bullosa, the clinical diagnosis took several months – and the exact diagnosis took as long as 14 years."
Living and Everyday Life with Rare Diseases
Many family members and especially social associates cannot imagine what a rare disease is and how it will progress. How they deal with the ill person and offer the person help in his/her daily life is a special challenge. Therefore, specialists who are able to offer the patient information about the course of the disease and therapy options are a great source of support.
Difficult to Access Specialists
The patients are frequently dependent on a very small number of specialists. In many cases the access to the specialists is rendered difficult by spatial distance; the patient may not be aware of the required expertise and the necessary specialised facilities or these may not be easy to find.
Patient organisations and self-help groups are a valuable means of exchanging experience among patients. A few patients desire more intensive exchange of experience with others, whereas others desire a more intensive doctor-patient relationship. The organisations take care of the Rare Disease Community while taking the patients‘ personal privacy into account.
Aspects of Therapy
Persons affected by rare diseases are frequently confronted with unsatisfactory therapy options or yet unapproved treatments. In many cases, suitable nursing measures can improve the patients‘ quality of life and also enhance their life expectancy. In part, impressive progress has been made in the treatment of some diseases. This shows that research work is not in vain; energy and resources should be invested in the targeted research of rare diseases.
95% of rare diseases
Development under the burden of barriers
The development of ideas and solutions in the field of rare diseases requires an international network. Only by combining know-how is it possible to define fields of action and introduce lasting measures.
How does the European Union deal with RARE DISEASES?
The EU regulation on drugs for the treatment of rare diseases came into force on 22 January 2000. Its purpose was to promote the research, development, and dissemination of medical products for rare diseases.
The rising numbers of orphan drugs (drugs that have been specifically developed for the treatment of rare diseases) show that companies like AOP Health are actively and increasingly focussed on the field of rare diseases. About 20% of the drugs approved in the EU every year are orphan drugs.
Sources:
European Medicines Agency (EMA) at: https://www.ema.europa.eu/en/human-regulatory/overview/orphan-designation-overview, retrieved on 9.1.2019
Pharmig | Association of the Pharmaceutical Industry of Austria at http://www.pharmig.at/DE/Der%20Verband/Fachbereiche/Seltene%20Erkrankungen/Seltene+Erkrankungen.aspx, retrieved on 9.1.2019
Interview with Dr. Rainer Riedl on 29.11.2018
Interview with Univ. Prof. Irene Lang, MD, on 15.11.2018
Interview with Ass.-Prof. Priv.-Doz. Dr. Stefan Seidel on 30.10.2018