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

Recruiting now · Phase 1

Conditions studied: Ovarian Cancer Recurrent, Ovarian Cancer, Platinum Resistant Ovarian Cancer

In brief

The goal of this clinical trial is to learn if OPB-101 is safe in platinum resistant ovarian cancer participants and also to find the optimal dose of OPB-101. Participants will have their own T cells modified in a laboratory and given back to them as OPB-101 in this one-time treatment. Participants will be in the hospital when they receive OPB-101 and then be checked at the clinical site frequently for the first few months.

Key facts

Study ID

NCT07030907

Run by

Outpace Bio, Inc.

People needed

30

Starts

2025-06-16

Expected to finish

2030-05-15

Last updated by the study team

2025-12-18

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• 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

You may not qualify if…

• 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

Where it is running

• Karmanos Cancer Institute — Detroit, Michigan, United States (enrolling)
• University of Minnesota — Minneapolis, Minnesota, United States (enrolling)
• Roswell Park — Buffalo, New York, United States (enrolling)
• MD Anderson Cancer Center — Houston, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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