Literature DB >> 28987289

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

Maria E Sheean1, Violeta Stoyanova-Beninska2, Giuseppe Capovilla3, Dinah Duarte4, Matthias P Hofer5, Michel Hoffmann6, Armando Magrelli7, Segundo Mariz5, Stelios Tsigkos5, Evyenia Shaili5, Benedetta Polsinelli5, Mario Ricciardi8, Milton Bonelli5, Pavel Balabanov5, Kristina Larsson5, Bruno Sepodes9.   

Abstract

Here, we provide an in-depth literature and experience-based review of nonclinical models and data used to support orphan medicinal product designations (OMPDs) in rare neurodegenerative conditions. The Committee for Orphan Medicinal Products (COMP) of the European Medicines Agency updates its assessment processes based on scientific progress and aims to provide transparent criteria required in support of OMPDs. Thus, we also provide an updated analysis of existing nonclinical models in selected conditions and identify key features of nonclinical studies that are crucial for the support of OMPDs. This could not only inform future drug development in rare neurological conditions, but also indicate areas where the use of nonclinical models can be made more efficient.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Mesh:

Year:  2017        PMID: 28987289     DOI: 10.1016/j.drudis.2017.09.015

Source DB:  PubMed          Journal:  Drug Discov Today        ISSN: 1359-6446            Impact factor:   7.851


  1 in total

Review 1.  Regulatory Standards in Orphan Medicinal Product Designation in the EU.

Authors:  Stelios Tsigkos; Segundo Mariz; Maria Elzbieta Sheean; Kristina Larsson; Armando Magrelli; Violeta Stoyanova-Beninska
Journal:  Front Med (Lausanne)       Date:  2021-06-25
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.