To compare and evaluate the efficacy and safety of Liporaxel® solution (oral paclitaxel) and Taxol® (IV paclitaxel) on recurrent or metastatic breast cancer.
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[Phase II] Objective Response Rate (ORR)
Timeframe: Participants will be followed every 6 weeks until progression, an expected average of 9 months.
[Phase III] Progression Free Survival (PFS)
Timeframe: From date of randomization, assessed up to 18 months.