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J Biopharm Stat. 2017;27(2):265-271. doi: 10.1080/10543406.2017.1275956. Epub 2016 Dec 27.

On hybrid parallel-crossover designs for assessing drug interchangeability of biosimilar products.

Author information

1
a Department of Biostatistics and Bioinformatics , Duke University School of Medicine , Durham , North Carolina , USA.
2
b Peking University Clinical Research Institute , Peking University , Beijing , China.

Abstract

In recent years, a specific hybrid parallel-crossover design that consists of two sequences of treatments, namely R-R-R-R and R-T-R-T, where T and R is a proposed biosimilar product and an innovative biological product, respectively, have been proposed and received much attention for assessing drug interchangeability between T and R, where R could be either a US-licensed product or an EU-reference product. In practice, there are three types of hybrid parallel-crossover designs that are commonly employed in assessing drug interchangeability of biosimilar products. These three types of parallel-crossover hybrid designs include (1) a parallel + 2 × 2 crossover design, (2) a parallel + 2 × 3 crossover design, and (3) a parallel + 2 × 4 crossover design. This article provides a comprehensive review of these study designs including a complete N-of-1 randomized trial design. A specific hybrid parallel-crossover design, that is, (RRRR, RTRT) for addressing drug interchangeability in terms of switching and the relative risk between with/without alternation is discussed.

KEYWORDS:

Alternation; N-of-1 trial design; by period analysis; by sequence analysis; switching

PMID:
28026996
DOI:
10.1080/10543406.2017.1275956
[Indexed for MEDLINE]

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