Methodologies in Biosimilar Product Development
eBook - ePub

Methodologies in Biosimilar Product Development

  1. 440 pages
  2. English
  3. ePUB (mobile friendly)
  4. Available on iOS & Android
eBook - ePub

Methodologies in Biosimilar Product Development

About this book

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  • Reviews withdrawn draft guidance on analytical similarity assessment.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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Yes, you can access Methodologies in Biosimilar Product Development by Sang Joon Lee, Shein-Chung Chow, Sang Joon Lee,Shein-Chung Chow in PDF and/or ePUB format, as well as other popular books in Mathematics & Pharmacology. We have over one million books available in our catalogue for you to explore.

Information

Edition
1
Subtopic
Pharmacology

Table of contents

  1. Cover
  2. Half Title
  3. Series Page
  4. Title Page
  5. Copyright Page
  6. Table of Contents
  7. Preface
  8. Authors
  9. Contributors
  10. 1. Biosimilar Product Development
  11. 2. CMC Considerations for Quality
  12. 3. Quality by Design
  13. 4. Stability Studies
  14. 5. Two One-Sided Tests Versus Confidence Interval Approach
  15. 6. Equivalence Test with Flexible Margin
  16. 7. Modified Quality Range Method for Analytical Similarity Evaluation
  17. 8. PK/PD Bridging Studies
  18. 9. Non-inferiority/Similarity Margin
  19. 10. Design and Analysis of Biosimilar Switching Studies
  20. 11. Detecting Reference Product Change in Biosimilar Studies
  21. 12. Sensitivity Analysis for Assessment of Extrapolation
  22. 13. Non-Medical Switch
  23. 14. Case Studies
  24. Index