| Literature DB >> 25033370 |
Masayuki Nagasaki1, Yuki Ando.
Abstract
In recent years, development of biosimilar products has attracted considerable attention. Because of the structural complexity of biologics, it is difficult to demonstrate that a biosimilar product is identical to the reference product. Therefore, for the development of biosimilar products, we need to adopt an approach that is different from generic product development. In this article, we discuss the guidelines for the development of biosimilar products along with the case examples of biosimilar product development in Japan. In addition, we discuss several issues of clinical trial design for demonstrating biosimilarity to a reference product.Keywords: Biosimilarity; Equivalence margin; Global clinical trial
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Year: 2014 PMID: 25033370 DOI: 10.1080/10543406.2014.941983
Source DB: PubMed Journal: J Biopharm Stat ISSN: 1054-3406 Impact factor: 1.051