About this trial
This study is a Prospective, Single-arm, Phase II clinical trial. The purpose of this study is to find out if taking Etoposide Capsules combined With Bevacizumab and Iparomlimab and Tuvonralimab is safe and works well for people with platinum-resistant or platinum refractory ovarian cancer . Researchers will look at the Progression-Free Survival, Objective Response Rate, Overall Survival, safety, and any side effects.
Eligibility criteria
Qualifiers
Age: 18-75, female;
According to RECIST 1.1 criteria, there are measurable lesions at baseline;
ECOG PS: 0-1;
Epithelial ovarian, fallopian tube, and primary peritoneal cancer with platinum resistance or platinum refractory recurrence; Provide 10 white films for pathological type confirmation and efficacy marker exploration, and meet all of the following conditions.
Disqualifiers
Patients who participate in other clinical trials simultaneously;
Allergic constitution, including a history of severe drug allergies or drug allergic reactions; Known to be allergic or intolerant to the investigational drug;
No measurable lesions or lesions that cannot be evaluated;
Patients with untreated central nervous system metastases, who have previously received systemic or curative treatment for brain or meningeal metastases (radiotherapy or surgery), have been confirmed stable for at least one month by imaging, and have stopped systemic hormone therapy (dose>10mg/day prednisone or other therapeutic hormones) for more than two weeks without clinical symptoms can be included;
Trial design
Treatments tested in this trial
- Etoposide Capsules
- Bevacizumab
- Iparomlimab and Tuvonralimab (QL1706)