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Methodologies in Biosimilar Product Development

Engelsk Paperback
SPAR
kr 63

Methodologies in Biosimilar Product Development

Engelsk Paperback

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  • Reviews withdrawn draft guidance on analytical similarity assessment.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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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.

Produktdetaljer
Sprog: Engelsk
Sider: 380
ISBN-13: 9781032071800
Indbinding: Paperback
Udgave:
ISBN-10: 103207180X
Kategori: Kliniske forsøg
Udg. Dato: 25 sep 2023
Længde: 0mm
Bredde: 234mm
Højde: 156mm
Forlag: Taylor & Francis Ltd
Oplagsdato: 25 sep 2023
Forfatter(e):
Forfatter(e)


Kategori Kliniske forsøg


Sprog Engelsk


Indbinding Paperback


Sider 380


Udgave


Længde 0mm


Bredde 234mm


Højde 156mm


Udg. Dato 25 sep 2023


Oplagsdato 25 sep 2023

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