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A pharmaceutical company plans to test a potiental anti-cancer drug on human subjects, The drug will...

A pharmaceutical company plans to test a potiental anti-cancer drug on human subjects, The drug will be administered in pill form. How would this study be designed so that appropriate controls are in place?
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A double blind randomised controlled trial should be conducted to test the efficacy of this potential anti-cancer drug. Informed written consent should be obtained from the study participants after explaining them in detail about the study. The cancer patients are randomised into two groups: study group and control group. The study group receives the anti-cancer drug and the control group receives the placebo. The data are collected which may include improvement in clinical profile of the study participants over a different time period. The data from the study group and control group are compared after eliminating confounding factors. The study results are then published.

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