What are the key phases of clinical trials, and how are they covered in Clinical Trials courses?

<p>The key phases of Clinical Trials course are:</p><ul><li dir="ltr"><strong>Phase I: </strong>This phase involves studying a new drug or treatment in a small number of people for the first time to evaluate its safety, dosage range, and side effects. The course will also explore how to conduct dose-escalation studies and monitor participants.</li><li dir="ltr"><strong>Phase II: </strong>This phase focuses on evaluating the treatment's effectiveness and continues to evaluate safety. In Phase II, students will study design, endpoints, and patient selection in greater detail.</li><li dir="ltr"><strong>Phase III: </strong>This phase is conducted in large populations to confirm effectiveness, monitor side effects, and compare it to standard treatments. During this phase of the course, we will discuss trial protocol development, data management, and regulatory submissions.</li><li dir="ltr"><strong>Phase IV: </strong>Post-marketing studies are also conducted to gather additional information about the drug's risks, benefits, and optimal use. The course will identify pharmacovigilance, long-term tracking of safety, and generating real-world evidence.</li></ul>

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