Biosimilarity The FDA Perspective
Auteur : Niazi Sarfaraz K.
Summary:
The focus of this book is on how the U.S. FDA will approve biosimilar drugs, as learned from recent approvals by the FDA. Understanding the limitations of the statutory limits and non-inferiority testing are presented as tools to obviate patient trials and minimize testing of immunogenicity. An in-depth scientific, mathematical and statistical view of the tools required to establish biosimilarity of biological drugs of different complexity -- a must for every developer of biosimilars.
Features:
First comprehensive analysis based on new guidelines and approval packages of several biosimilars
Presents the first approach to challenge FDA in reducing or eliminating any testing in patients.
Provides a comprehensive understanding of the U.S. statutory requirements vis-a-vis the regulatory guidelines
Provides model CQA and Analytical Similarity testing protocols for cytokines and monoclonal antibodies
Allow creation of a fast-to-market pathway to develop biosimilars
Current Status of Biosimilar Biological Products. The FDA Position. Biosimilarity Tetrahedron. Analytical and Functionality Similarity. Non-clinical Assessment. Clinical Pharmacology Assessment. Clinical Studies. Interchangeability Status. Comprehensive Presentation
Sarfaraz K. Niazi Ph.D, is Adjunct Professor at the faculty of University of Houston as well Chairman and President of Therapeutic Proteins Inc.
Date de parution : 06-2024
17.8x25.4 cm
Date de parution : 08-2018
17.8x25.4 cm
Thème de Biosimilarity :
Mots-clés :
Biosimilar Product; Generic Drug Development; Reference Product; Generic Drug Approval Process; BPCI Act; Biosimiars Manufacturing; Biosimilar Developer; FDA Regulations for Biosimilars; Biological Product; Drug Development Regulations; Analytical Similarity Assessment; Ich Q8; Biosimilar Candidate; Clinical Pharmacology Studies; Ich Q6B; Sialic Acid; BLA; Container Closure Systems; LMWH; FDA Guidance; Residual Uncertainty; Residual DNA; Ich Q5E; Reference Medicinal Product; PD Similarity; Reversible Self-association; Native Page; PHS Act; FDA Risk; Tolerance Breakdown