Contribution to a book DZNE-2020-00765

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Chapter 4 - Therapies for prion diseases

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2019
Elsevier

Handbook of Clinical Neurology Elsevier 165, 47 - 58 ()

Abstract: Recent advances in understanding of the molecular biology of prion diseases and improved clinical diagnostic techniques might allow researchers to think about therapeutic trials in Creutzfeldt–Jakob disease (CJD) patients. Some attempts have been made in the past and various compounds have been tested in single case reports and patient series. Controlled trials are rare. However, in the past few years, it has been demonstrated that clinical trials are feasible. The clinicians might face several specific problems when evaluating the efficacy of the drug in CJD, such as rareness of the disease, lack of appropriate preclinical tests and heterogeneous clinical presentation in humans. These problems have to be carefully addressed in future.


Contributing Institute(s):
  1. Ext UMG Zerr (Ext UMG Zerr)
  2. Göttingen Pre 2020 (Göttingen Pre 2020)
  3. Translational Studies and Biomarkers (AG Zerr)
Research Program(s):
  1. 344 - Clinical and Health Care Research (POF3-344) (POF3-344)

Appears in the scientific report 2019
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Document types > Books > Contribution to a book
Institute Collections > GÖ DZNE > GÖ DZNE-Ext UMG Zerr
Institute Collections > GÖ DZNE > GÖ DZNE-AG Zerr
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 Record created 2020-08-04, last modified 2020-09-25


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