
Methodologies in Biosimilar Product Development
- 440 pages
- English
- ePUB (mobile friendly)
- Available on iOS & Android
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- Reviews withdrawn draft guidance on analytical similarity assessment.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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Information
Table of contents
- Cover
- Half Title
- Series Page
- Title Page
- Copyright Page
- Table of Contents
- Preface
- Authors
- Contributors
- 1. Biosimilar Product Development
- 2. CMC Considerations for Quality
- 3. Quality by Design
- 4. Stability Studies
- 5. Two One-Sided Tests Versus Confidence Interval Approach
- 6. Equivalence Test with Flexible Margin
- 7. Modified Quality Range Method for Analytical Similarity Evaluation
- 8. PK/PD Bridging Studies
- 9. Non-inferiority/Similarity Margin
- 10. Design and Analysis of Biosimilar Switching Studies
- 11. Detecting Reference Product Change in Biosimilar Studies
- 12. Sensitivity Analysis for Assessment of Extrapolation
- 13. Non-Medical Switch
- 14. Case Studies
- Index