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Mouse Models of Lung Fibrosis
Journal article

Mouse Models of Lung Fibrosis

Abstract

The drug discovery pipeline, from discovery of therapeutic targets through preclinical and clinical development phases, to an approved product by health authorities, is a time-consuming and costly process, where a lead candidates’ success at reaching the final stage is rare. Although the time from discovery to final approval has been reduced over the last decade, there is still potential to further optimize and streamline the evaluation process of each candidate as it moves through the different development phases. In this book chapter, we describe our preclinical strategies and overall decision-making process designed to evaluate the tolerability and efficacy of therapeutic candidates suitable for patients diagnosed with fibrotic lung disease. We also describe the benefits of conducting preliminary discovery trials, to aid in the selection of suitable primary and secondary outcomes to be further evaluated and assessed in subsequent internal and external validation studies. We outline all relevant research methodologies and protocols routinely performed by our research group and hope that these strategies and protocols will be a useful guide for biomedical and translational researchers aiming to develop safe and beneficial therapies for patients with fibrotic lung disease.

Authors

Mekhael O; Naiel S; Vierhout M; Hayat AI; Revill SD; Abed S; Inman MD; Kolb MRJ; Ask K

Journal

Methods in Molecular Biology, Vol. 2299, , pp. 291–321

Publisher

Springer Nature

Publication Date

January 1, 2021

DOI

10.1007/978-1-0716-1382-5_21

ISSN

1064-3745
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