This clinical trial is focused on studying the effectiveness and safety of a new treatment called luveltamab tazevibulin (also known as STRO-002) for women with a type of cancer known as relapsed platinum-resistant epithelial ovarian cancer. This includes cancers that originate in the ovaries, fallopian tubes, or the lining of the abdomen, known as the peritoneum. The study will compare this new treatment to standard chemotherapy options chosen by the doctor, which may include medications like gemcitabine, paclitaxel, topotecan, or Caelyx (pegylated liposomal doxorubicin).
The purpose of the study is to evaluate how well luveltamab tazevibulin works compared to these standard treatments. Participants will receive either the new treatment or one of the standard chemotherapy options. The study will monitor the participants over a period of time to assess the treatment’s impact on the cancer and any side effects that may occur. The study will also use a special test called the VENTANA FOLR1 CDx Assay to identify patients who might benefit from the new treatment. This test checks for the presence of a protein called folate receptor alpha in the cancer cells.
Throughout the study, participants will receive their assigned treatment and undergo regular check-ups to monitor their health and the cancer’s response to the treatment. The study aims to provide valuable information on whether luveltamab tazevibulin can be a more effective option for treating this type of ovarian cancer compared to existing chemotherapy treatments. The study is expected to continue until 2027, with recruitment starting in 2024.



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