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PPS is the only FDA-approved oral agent for the treatment of IC/BPS and is by far the most-studied oral medication in use for IC/BPS

The DXN group was administered an intraperitoneal dose of 5 mg/kg body weight (BW) for four cycles (cumulative dose 20 mg/kg), with each cycle separated by a three-day interval, and this dosage was consistent with the therapeutic levels typically administered to individuals receiving cancer treatment (Zhong et al., 2023

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All-in-one nanotheranostic platform based on tumor microenvironment: new strategies in multimodal imaging and therapeutic protocol