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Carte Methodologies in Biosimilar Product Development Sang Joon Lee

Methodologies in Biosimilar Product Development

Autor: Sang Joon Lee, Shein-Chung Chow
Limbă: engleză
Legare: Carte broșată
Editura: Taylor & Francis Ltd
Disponibilitate: În depozitul extern
Expediem în 9-15 zile
371.90 lei
Methodologies for Biosimilar Product Development covers the practical and challenging issues that ar...

Informații despre carte

Autor
Sang Joon Lee, Shein-Chung Chow
Limbă
engleză
Legare
Carte - Carte broșată
Publicat
2023
Pagini
380
EAN
9781032071800
Enbook ID
43908221
Editura
Taylor & Francis Ltd
Greutate
453
Dimensiuni
156 x 234

Descriere completă

Methodologies for Biosimilar Product Development covers the practical and challenging issues that are commonly encountered during the development, review, and approval of a proposed biosimilar product. These practical and challenging issues include, but are not limited to the mix-up use of interval hypotheses testing (i.e., the use of TOST) and confidence interval approach, a risk/benefit assessment for non-inferiority/similarity margin, PK/PD bridging studies with multiple references, the detection of possible reference product change over time, design and analysis of biosimilar switching studies, the assessment of sensitivity index for assessment of extrapolation across indications without collecting data from those indications not under study, and the feasibility and validation of non-medical switch post-approval.


Key Features:



  • Reviews withdrawn draft guidance on analytical similarity assessment.

  • Evaluates various methods for analytical similarity evaluation based on FDA's current guidelines.

  • Provides a general approach for the use of n-of-1 trial design for assessment of interchangeability.

  • Discusses the feasibility and validity of the non-medical switch studies.

  • Provides innovative thinking for detection of possible reference product change over time.

This book embraces innovative thinking of design and analysis for biosimilar studies, which are required for review and approval of biosimilar regulatory submissions.

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