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Study design: The study is planning to enroll male and female subjects affected by genital lesions, in particular to collect 200 scrapes/biopsies from women with normal ectocervical epithelium as well as with all different degrees of ectocervical lesions (from CIN 1/LSIL to cervical carcinoma).
An ongoing American study is planning to enroll up to 3,400 premenopausal and postmenopausal women with HR+/HER2- breast cancer who have received prior standard neoadjuvant or adjuvant chemotherapy.
As with all assays, the starting point for developing a microarray study is planning the comparisons that will be made, and the simplest experimental designs are based on the comparative analysis of two classes of samples, either using a series of paired case-control comparisons, or comparisons to a common reference sample, although other approaches have been described.
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A more detailed general study is planned for the future.
A separate toxicity study is planned to answer this question.
A larger-scale study is planned [ 25].
A phase III study is planned.
The study is planned to end mid 2014.
A larger validation study is planned.
A prospective comparative study is planned.
The study is planned as a prospective simulated study.
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