Nonclinical data supporting orphan medicinal product designations: lessons from rare neurological conditions

2018 ◽  
Vol 23 (1) ◽  
pp. 26-48 ◽  
Author(s):  
Maria E. Sheean ◽  
Violeta Stoyanova-Beninska ◽  
Giuseppe Capovilla ◽  
Dinah Duarte ◽  
Matthias P. Hofer ◽  
...  
2013 ◽  
Vol 60 (Supplementum-VIII) ◽  
pp. 26-31 ◽  
Author(s):  
T. Foltánová ◽  
M. Mazág

Medical and scientific knowledge about rare diseases is minimal or lacking, thus making research difficulties for pharmaceutical industry. Orphan drugs in EU are under supervision of European Commission, European medical agency (EMA) and Committee for orphan medicinal products (COMP). The presentation provides a brief review of all supportive incentives in the field of orphan medicinal products as: the European orphan medicinal product (OMP) regulation, Guideline on Clinical Trials in Small Populations and Commission Regulation (EC) No 2049/2005 / support of small and medium enterprises (SMEs). It also introduces the concept of Clinical added value of orphan medicinal products, as one of the key instruments to increase the availability of orphan medicinal products in the member states. Separately it stresses the necessity of Health technology assessment implementation in whole process of orphan medicinal product development as well as the implementation of the Europlan indicators into the Slovak National plan


2020 ◽  
Vol 25 (2) ◽  
pp. 274-291 ◽  
Author(s):  
Maria E. Sheean ◽  
Eva Malikova ◽  
Dinah Duarte ◽  
Giuseppe Capovilla ◽  
Laura Fregonese ◽  
...  

2020 ◽  
Vol 13 (12) ◽  
pp. 425
Author(s):  
Anna Maria Piras ◽  
Ylenia Zambito ◽  
Maurizio Lugli ◽  
Baldassare Ferro ◽  
Paolo Roncucci ◽  
...  

The SARS-CoV-2 infection is associated with pulmonary coagulopathy, which determines the deposition of fibrin in the air spaces and lung parenchyma. The resulting lung lesions compromise patient pulmonary function and increase mortality, or end in permanent lung damage for those who have recovered from the COVID-19 disease. Therefore, local pulmonary fibrinolysis can be efficacious in degrading pre-existing fibrin clots and reducing the conversion of lung lesions into lasting scars. Plasminogen is considered a key player in fibrinolysis processes, and in view of a bench-to-bedside translation, we focused on the aerosolization of an orphan medicinal product (OMP) for ligneous conjunctivitis: human plasminogen (PLG-OMP) eye drops. As such, the sterile and preservative-free solution guarantees the pharmaceutical quality of GMP production and meets the Ph. Eur. requirements of liquid preparations for nebulization. PLG-OMP aerosolization was evaluated both from technological and stability viewpoints, after being submitted to either jet or ultrasonic nebulization. Jet nebulization resulted in a more efficient delivery of an aerosol suitable for pulmonary deposition. The biochemical investigation highlighted substantial protein integrity maintenance with the percentage of native plasminogen band > 90%, in accordance with the quality specifications of PLG-OMP. In a coherent way, the specific activity of plasminogen is maintained within the range 4.8–5.6 IU/mg (PLG-OMP pre-nebulization: 5.0 IU/mg). This is the first study that focuses on the technological and biochemical aspects of aerosolized plasminogen, which could affect both treatment efficacy and clinical dosage delivery. Increasing evidence for the need of local fibrinolytic therapy could merge with the availability of PLG-OMP as an easy handling solution, readily aerosolizable for a fast translation into an extended clinical efficacy assessment in COVID-19 patients.


2018 ◽  
Vol 23 (3) ◽  
pp. 681-686 ◽  
Author(s):  
Stelios Tsigkos ◽  
Matthias Philipp Hofer ◽  
Maria Elzbieta Sheean ◽  
Segundo Mariz ◽  
Kristina Larsson ◽  
...  

2021 ◽  
Vol 8 ◽  
Author(s):  
Stelios Tsigkos ◽  
Segundo Mariz ◽  
Maria Elzbieta Sheean ◽  
Kristina Larsson ◽  
Armando Magrelli ◽  
...  

Twenty years of orphan regulation in Europe have now elapsed, with almost 2,400 orphan designated medicinal products and more than 190 orphan products authorised in the EU. Alongside the evolution in understanding of rare diseases, considerable regulatory knowledge has also been accumulated regarding the level of evidence that would support inclusion of products into the framework. This article reviews publications and regulatory documents pertaining to orphan medicinal product designation in the EU and discusses the general expectations in submitted applications as reflected in the current regulatory practise. Important elements to recommend granting a European orphan designation are the key considerations of orphan condition, medical plausibility, seriousness, and prevalence, while significant benefit is also assessed when there are authorised medicinal products for the sought indication. This review attempts to clarify the specific concepts currently used in that regard and discusses how the available data can be used to justify the criteria for designation. Moving away from theoretical expectations or assumptions, it stresses that the applications have to be complemented with nosological and epidemiological justifications pertaining to the proposed condition, as well as relevant data in specific non-clinical in vivo models or in affected patients to support inclusion into the orphan scheme.


Sign in / Sign up

Export Citation Format

Share Document