Study on the Safety and Effectiveness of TORL-1-23 with Chemotherapy Before Surgery in Women with Advanced Ovarian Cancer
Sponsor: TORL Biotherapeutics, LLC
Sponsor score: 0
ClinicalTrials ID:NCT07322094
This clinical trial is testing a new treatment, TORL-1-23, combined with chemotherapy, to see if it is safe and effective when given before surgery in women with advanced ovarian cancer.
Patient Parameters
| Parameter | Options |
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Program Overview
The purpose of this study is to evaluate the safety and effectiveness of a new treatment called TORL-1-23, used together with chemotherapy, in women who have advanced stage ovarian cancer. The treatment is given before the initial surgery to see if it can help manage the cancer better.
Eligibility Criteria
Inclusion Criteria
- Women with a good overall health status, as measured by a performance score of 2 or less.
- Diagnosed with epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer.
- Cancer must be at an advanced stage (FIGO Stage III or IV).
- Cancer cells must show a specific marker called claudin 6 (CLDN6).
- Must have adequate organ function as determined by medical tests.
Exclusion Criteria
- Have certain types of ovarian cancer, such as clear cell, mucinous, sarcomatous, mixed histology, low-grade/borderline, or non-epithelial.
- Have received any prior systemic treatment for the ovarian cancer being studied.
- Have had previous surgery for the cancer.
- Have had radiation therapy to the abdomen or pelvis.
- Are currently receiving or have recently received chemotherapy, targeted therapy, or immunotherapy for any condition.
- Have active, worsening, or symptomatic cancer spread to the brain.
- Have serious, uncontrolled medical conditions or active infections that make them a poor candidate for the study.
- Are pregnant or breastfeeding.
Locations
| FACILITY | ZIP | CITY | STATE |
|---|---|---|---|
| UCLA | 90095 | Los Angeles | California |
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