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Introduction:

Oral biologic drugs have become an increasingly important area of research in the field of pharmacology and drug development. Biologic drugs are large molecules derived from living organisms, such as antibodies, proteins, or nucleic acids, and have revolutionized the treatment of various diseases, including autoimmune disorders, cancer, and infectious diseases. While most biologic drugs are administered through injections or infusions, the development of oral biologics presents a promising alternative that could improve patient compliance, convenience, and overall treatment outcomes.

This thesis aims to explore the current status and challenges of developing oral biologic drugs, with a focus on the underlying mechanisms, formulation strategies, and clinical implications. By conducting a comprehensive review of the existing literature and presenting original research findings, this study seeks to contribute to the growing body of knowledge in this rapidly evolving field.

Table of contents:

Chapter 1: Introduction
1.1 Introduction
1.2 Background of study
1.3 Problem Statement
1.4 Objective of study
1.5 Limitation of study
1.6 Scope of study
1.7 Significance of study
1.8 Structure of the Thesis
1.9 Definition of terms

Chapter 2: Literature Review
2.1 Overview of oral biologic drugs
2.2 Mechanisms of action
2.3 Formulation and delivery challenges
2.4 Clinical applications
2.5 Regulatory considerations
2.6 Current trends and future directions
2.7 Case studies
2.8 Challenges and opportunities
2.9 Gaps in the literature
2.10 Summary of key findings

Chapter 3: Research Methodology
3.1 Research design
3.2 Data collection methods
3.3 Sample selection
3.4 Data analysis techniques
3.5 Ethical considerations
3.6 Pilot testing
3.7 Validity and reliability
3.8 Limitations of the methodology

Chapter 4: Discussion of Findings
4.1 Overview of research findings
4.2 Comparison with existing literature
4.3 Implications for drug development
4.4 Potential clinical applications
4.5 Recommendations for future research
4.6 Strengths and limitations of the study
4.7 Conclusion

Chapter 5: Conclusion and Summary
5.1 Summary of key findings
5.2 Implications for practice
5.3 Contributions to the field
5.4 Recommendations for further research
5.5 Conclusion

Thesis Overview:

The development of oral biologic drugs holds great promise for improving the treatment of various diseases by providing a more convenient and patient-friendly alternative to traditional injectable biologics. This thesis aims to explore the current landscape of oral biologic drug development, including the underlying mechanisms, formulation strategies, clinical implications, and regulatory considerations. Through a comprehensive literature review and original research, this study seeks to contribute to our understanding of the challenges and opportunities in this emerging field.

Chapter 1 provides an introduction to the topic, outlining the background of the study, the problem statement, objectives, limitations, scope, significance, and structure of the thesis. Chapter 2 offers a detailed review of the existing literature on oral biologic drugs, covering mechanisms of action, formulation challenges, clinical applications, regulatory issues, current trends, and future directions. Chapter 3 discusses the research methodology employed in this study, including research design, data collection methods, sample selection, analysis techniques, ethical considerations, and limitations.

In Chapter 4, the findings of the study are presented and discussed in detail, with a focus on their implications for drug development, clinical applications, and future research directions. Finally, Chapter 5 summarizes the key findings, discusses their implications for practice, highlights the contributions of the study to the field, offers recommendations for further research, and concludes the thesis.

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