Endometrial Cancers

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Review clinical trials related to Endometrial Cancers. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

A Phase 1 Study to Evaluate the Safety and Efficacy of OPB-201 in Recurrent Endometrial and Platinum-resistant Ovarian Cancer.

The goal of this clinical trial is to learn if OPB-201 is safe in recurrent endometrial and platinum resistant ovarian cancer participants and also to find the optimal dose of OPB-201. Participants will have their own T cells modified in a laboratory and given back to them as OPB-201 in this one-time treatment. Participants will be in the hospital when they receive OPB-201 and then be checked at the clinical site frequently for the first few months.

Participants needed: 30
Trial details
Phase: Phase 1Age: 18+Biological sex: FemaleType: InterventionalSponsor: Outpace Bio, Inc.Updated: Jun 24, 2026
Eligibility criteria

Age ≥ 18 years of age at the time of signing the informed consent form. [+9]

Women of child-bearing potential who are pregnant or breastfeeding. [+9]

Status: Not yet recruiting

Near-Infrared Fluorescence Imaging With Indocyanine Green to Evaluate Bowel Anastomoses in Gynecologic Oncology Surgery

The goal of this study is to evaluate if indocyanine green (ICG) fluorescence imaging helps reduce complications in bowel surgery performed during gynecologic cancer operations. The main question it aims to answer is: Does using ICG fluorescence imaging during bowel anastomosis reduce the rate of complications such as leaks, infections, and abscesses within 30 days after surgery? Participants are women aged 18 and older undergoing surgery for gynecologic cancers (such as ovarian, uterine, cervical, or vulvar cancer). During surgery, investigators will inject ICG intravenously, then use a special near-infrared camera to see how well blood flows at the anastomosis site. The investigators will then decide if the reconnection is good enough or needs adjustment. Researchers will record any complications within the first 30 days after surgery to understand if this imaging method helps reduce surgical risks.

Participants needed: 50
Trial details
Phase: Phase 4Age: 18+Biological sex: FemaleType: InterventionalSponsor: Istanbul UniversityUpdated: Mar 14, 2025Locations: 1
Eligibility criteria

Female patients aged 18 years or older. [+3]

Known allergy or hypersensitivity to indocyanine green (ICG). [+2]