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A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary...

A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_rcaap_revistas_10451_48439

A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary transthyretin-mediated (hATTR) amyloidosis

About this item

Full title

A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary transthyretin-mediated (hATTR) amyloidosis

Publisher

Springer Nature

Journal title

Orphanet journal of rare diseases, 2020, Vol.15 (1), p.179

Language

English

Formats

Publication information

Publisher

Springer Nature

More information

Scope and Contents

Contents

© The Author(s). 2020. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Background: Patisiran, an RNA interference therape...

Alternative Titles

Full title

A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary transthyretin-mediated (hATTR) amyloidosis

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_rcaap_revistas_10451_48439

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_rcaap_revistas_10451_48439

Other Identifiers

E-ISSN

1750-1172

DOI

10.1186/s13023-020-01399-4

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