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Preferably to account for the psychological effects of receiving treatments, the trial is conducted in a double-blinded fashion. Volunteers presenting with a cancerous condition, for example, chronic myeloid leukemia, are randomly assigned to placebo or treatment groups. Furthermore, to prevent the doctors from being biased in treatments, they are not informed as to whether the medication they are administering is the topical pharmaceutical composition of the present invention or a topical placebo. Using this randomization approach, each volunteer has the same chance of being given either the new treatment or the placebo.

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