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This drug is a combination of three distinct oral chemotherapeutic agents: **D07001** (an absorption-enhanced oral formulation of gemcitabine using self-microemulsifying technology), **capecitabine** (an oral prodrug of 5-fluorouracil used widely in gastrointestinal and breast cancers), and **TS-1/S-1** (an oral fluoropyrimidine combining tegafur, gimeracil, and oteracil to provide sustained 5-fluorouracil release while reducing gastrointestinal toxicity). - **D07001** acts as an oral bioavailable gemcitabine, a nucleoside analog inhibiting DNA synthesis in cancer cells[1][3][5][7]. - **Capecitabine** is a 5-fluorouracil prodrug that interferes with DNA synthesis[6]. - **TS-1** leverages tegafur (prodrug of 5-FU), gimeracil (DPD inhibitor to increase 5-FU plasma levels), and oteracil (reduces gastrointestinal side effects) for anti-tumor effects[2][4][6]. This combination aims to provide multifaceted inhibition of DNA synthesis and cell replication, potentially with complementary safety and efficacy profiles.
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