A Study to Evaluate the Safety and Efficacy of OPB-101 in Platinum-resistant Ovarian Cancer

Inclusion Criteria

• Age ≥ 18 years of age at the time of signing the informed consent form.
• Histologically confirmed diagnosis of high grade serous epithelial ovarian, peritoneal, or fallopian tube cancer based on local histopathological findings.
• Recurrent platinum-resistant disease defined as: Disease that has recurred within 6 months of the last receipt of platinum-based therapy.
• Received at least 2 prior lines of systemic chemotherapy including a platinum-based chemotherapy.
• Received prior therapy with a PARP inhibitor if the subject has a known germline or somatic BRCA1/2 mutation.
• Measurable disease.
• Consent to provide archived tumor tissue sample.
• ECOG performance status of 0 or 1.
• Adequate organ function.
• Alkaline phosphatase ≤ 2.5 x ULN
• ≤ Grade 1 dyspnea and oxygen saturation levels (SpO2) > 92% on room air.
• LVEF ≥ 50%
• Life expectancy of ≥ 3 months
• Adequate venous access.
• Negative screen for infectious disease markers.
• Negative serum pregnancy test.
• Abstain from heterosexual activity or to use 2 forms of effective methods of contraception. Note: Other protocol defined inclusion criteria could apply

Exclusion Criteria

• Women of child-bearing potential who are pregnant or breastfeeding.
• Uncontrolled bacterial, fungal, or viral infections.
• Active infection requiring systemic therapy.
• Bleeding or thrombotic disorders or at risk for severe hemorrhage.
• Any form of primary immunodeficiency.
• Had an allogenic tissue/solid organ transplant.
• Active autoimmune disease.
• Concurrent treatment with systemic high dose corticosteroids.
• Unresolved acute effects of any prior therapy.
• Active invasive cancer other than the cancer under study.
• Significant lung disease.
• Clinically significant pericardial effusion.
• Prior radiotherapy within 2 weeks of start of study intervention.
• No major surgery within 28 days prior to enrollment.
• Received investigational agents or tumor vaccines.
• Received chemotherapy within the previous 3 weeks.
• History of grade ≥ 3 ascites.
• Active CNS involvement.
• Received a live vaccine within 30 days prior to study treatment.
• Received prior CAR T cell therapy.
• Received prior mesothelin targeted therapy.
• Dependent on intravenous hydration or total parenteral nutrition. Note: Other protocol defined exclusion criteria could apply