Figure 1.

A consort diagram of this trial. A total of 91 women was randomly assigned to either TOR120 (n = 46) or EXE (n = 45), who were analyzed as intention-to-treat (ITT) cohort. Three of the 46 patients in the TOR120 were not received treatment, 2 patients having withdrawn from the trial by their preference and one having been dropped due to administration of another SERM. Except for these 3 cases, 43 cases of TOR120 were analyzed the efficacy and safety as ‘treatment-received’ cohort. Three of 43 treatment-received patients with TOR120 were dropped out of TOR120 early because of adverse effects.