What are the phases of the clinical trial process?
What are the phases of the clinical trial
process?
<p>
<p>There are three primary phases an investigational drug has to go through before it can be approved by the Food and Drug Administration (FDA), and a fourth phase that an
approved drug may enter. Phase I</p>
<p>In this phase of a clinical trial, the manufacturer wants to find out how the drug works in healthy study participants. Mode of action (how the drug exerts its effects),
safety, and side effects-these are some of the main issues that are of the utmost concern to drug makers at this stage of the clinical trial process. It is important to note
that in Phase I studies, the overall safety of the medication in patients has not been established.</p>
<p>Phase II</p>
<p>A drug gets to Phase II only when the FDA has reviewed the Phase I data and concludes that the drug is safe for patients, and that its clinical activity may be beneficial
against a particular disease or condition. At this point, a larger group of patients are enrolled and condition- or disease-specific rating scales are used to record data.</p>
<p>Phase III</p>
<p>This is an important turning point for drug manufacturers. The medication has already past the rigorous testing and review process required by the FDA, and now it's ready
to be studied in an even larger patient population, with even more advanced rating scales and clinical measures. In recent years, there has been a growing industry trend to
not only measure clinical effectiveness at this phase, but also measure "real world" results. For example, if a patient shows clinical improvement after entering
the study, how are their activities of daily living improving (i.e., the patient can work in the garden more often or attend their child's games on a regular basis)? Most
medications that make it to Phase III will at least be considered for approval by an FDA advisory board.</p>
<p>Phase IV</p>
<p>At this phase in development, the drug has already been granted FDA approval. Phase IV studies are often performed to either identify an additional use for an already
approved drug, or to gather additional safety information from a larger group of patients. In some cases, Phase IV studies are implemented to establish effectiveness in a
subgroup of patients, for example, patients over age 65.</p>
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