Biosimilars Development Strategies
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Biosimilars Development Strategies
Fast to Market Approaches
Niazi, Sarfaraz K.
Taylor & Francis Ltd
07/2024
188
Dura
9781032517018
Pré-lançamento - envio 15 a 20 dias após a sua edição
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Preface
Chapter 1 All About Biosimilars
1. Introduction
2. Approvals
3. Future Candidates
4. Approval Guidelines
5. Waivers
6. Appendix: Terminology
7. Appendix 2: Therapeutic Proteins approved by the FDA: potential biosimilar candidates.
8. Bibliography
Chapter 2 Product Type and Selection Strategies
1. Background
2. Exclusivity
3. Formulation
4. Route of Administration
5. Reference Product
Chapter 3 Development Master Plan
1. Introduction
2. Creating a Plan
3. Intellectual Property
4. Expression System
5. Release Specification
6. Nonclinical Testing
7. Clinical Pharmacology Assessment
8. Clinical Immunogenicity Assessment
9. Clinical Efficacy Assessment
10. Extrapolation of Clinical Data Across Indications
11. Interchangeability and Substitution
Chapter 4 Optimization of Cost of Goods
1. Background
2. Creation of Cell Lines
3. Media
4. Containers and Mixing Systems
5. Working downstream
6. Regulatory
7. Ongoing Production
8. Continuous Manufacturing
Chapter 5 Strategic Understanding for Biosimilars Future
1. Introduction
2. The Role of the US Congress
3. The Role of the FDA
4. The Role of Developers
5. The Role of the Associations
6. Conclusions
Chapter 6 Repurposing Biosimilars
1. Introduction
2. Understanding Therapeutic Proteins
3. Reinvention Scope
4. Intellectual Property
5. Artificial Intelligence (AI) and Machine Learning (ML)
6. Structure Prediction
7. Target identification
8. Molecular Docking
9. Drug Conjugates
10. Regulatory Perspective
11. Conclusions
12. References
Chapter 1 All About Biosimilars
1. Introduction
2. Approvals
3. Future Candidates
4. Approval Guidelines
5. Waivers
6. Appendix: Terminology
7. Appendix 2: Therapeutic Proteins approved by the FDA: potential biosimilar candidates.
8. Bibliography
Chapter 2 Product Type and Selection Strategies
1. Background
2. Exclusivity
3. Formulation
4. Route of Administration
5. Reference Product
Chapter 3 Development Master Plan
1. Introduction
2. Creating a Plan
3. Intellectual Property
4. Expression System
5. Release Specification
6. Nonclinical Testing
7. Clinical Pharmacology Assessment
8. Clinical Immunogenicity Assessment
9. Clinical Efficacy Assessment
10. Extrapolation of Clinical Data Across Indications
11. Interchangeability and Substitution
Chapter 4 Optimization of Cost of Goods
1. Background
2. Creation of Cell Lines
3. Media
4. Containers and Mixing Systems
5. Working downstream
6. Regulatory
7. Ongoing Production
8. Continuous Manufacturing
Chapter 5 Strategic Understanding for Biosimilars Future
1. Introduction
2. The Role of the US Congress
3. The Role of the FDA
4. The Role of Developers
5. The Role of the Associations
6. Conclusions
Chapter 6 Repurposing Biosimilars
1. Introduction
2. Understanding Therapeutic Proteins
3. Reinvention Scope
4. Intellectual Property
5. Artificial Intelligence (AI) and Machine Learning (ML)
6. Structure Prediction
7. Target identification
8. Molecular Docking
9. Drug Conjugates
10. Regulatory Perspective
11. Conclusions
12. References
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
Animal and efficacy testing;Recombinant engineering patent;Evolution of regulatory guidelines;Analysis of EU and FDA-approved products;Contract development and manufacturing organizations;Safety and efficacy of biosimilars
Preface
Chapter 1 All About Biosimilars
1. Introduction
2. Approvals
3. Future Candidates
4. Approval Guidelines
5. Waivers
6. Appendix: Terminology
7. Appendix 2: Therapeutic Proteins approved by the FDA: potential biosimilar candidates.
8. Bibliography
Chapter 2 Product Type and Selection Strategies
1. Background
2. Exclusivity
3. Formulation
4. Route of Administration
5. Reference Product
Chapter 3 Development Master Plan
1. Introduction
2. Creating a Plan
3. Intellectual Property
4. Expression System
5. Release Specification
6. Nonclinical Testing
7. Clinical Pharmacology Assessment
8. Clinical Immunogenicity Assessment
9. Clinical Efficacy Assessment
10. Extrapolation of Clinical Data Across Indications
11. Interchangeability and Substitution
Chapter 4 Optimization of Cost of Goods
1. Background
2. Creation of Cell Lines
3. Media
4. Containers and Mixing Systems
5. Working downstream
6. Regulatory
7. Ongoing Production
8. Continuous Manufacturing
Chapter 5 Strategic Understanding for Biosimilars Future
1. Introduction
2. The Role of the US Congress
3. The Role of the FDA
4. The Role of Developers
5. The Role of the Associations
6. Conclusions
Chapter 6 Repurposing Biosimilars
1. Introduction
2. Understanding Therapeutic Proteins
3. Reinvention Scope
4. Intellectual Property
5. Artificial Intelligence (AI) and Machine Learning (ML)
6. Structure Prediction
7. Target identification
8. Molecular Docking
9. Drug Conjugates
10. Regulatory Perspective
11. Conclusions
12. References
Chapter 1 All About Biosimilars
1. Introduction
2. Approvals
3. Future Candidates
4. Approval Guidelines
5. Waivers
6. Appendix: Terminology
7. Appendix 2: Therapeutic Proteins approved by the FDA: potential biosimilar candidates.
8. Bibliography
Chapter 2 Product Type and Selection Strategies
1. Background
2. Exclusivity
3. Formulation
4. Route of Administration
5. Reference Product
Chapter 3 Development Master Plan
1. Introduction
2. Creating a Plan
3. Intellectual Property
4. Expression System
5. Release Specification
6. Nonclinical Testing
7. Clinical Pharmacology Assessment
8. Clinical Immunogenicity Assessment
9. Clinical Efficacy Assessment
10. Extrapolation of Clinical Data Across Indications
11. Interchangeability and Substitution
Chapter 4 Optimization of Cost of Goods
1. Background
2. Creation of Cell Lines
3. Media
4. Containers and Mixing Systems
5. Working downstream
6. Regulatory
7. Ongoing Production
8. Continuous Manufacturing
Chapter 5 Strategic Understanding for Biosimilars Future
1. Introduction
2. The Role of the US Congress
3. The Role of the FDA
4. The Role of Developers
5. The Role of the Associations
6. Conclusions
Chapter 6 Repurposing Biosimilars
1. Introduction
2. Understanding Therapeutic Proteins
3. Reinvention Scope
4. Intellectual Property
5. Artificial Intelligence (AI) and Machine Learning (ML)
6. Structure Prediction
7. Target identification
8. Molecular Docking
9. Drug Conjugates
10. Regulatory Perspective
11. Conclusions
12. References
Este título pertence ao(s) assunto(s) indicados(s). Para ver outros títulos clique no assunto desejado.
