Metastatic Ovarian Cancer

5

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

Condition / disease
Location
Status: Recruiting

Immunotherapy Using Tumor Infiltrating Lymphocytes for Patients With Metastatic Cancer

Background: The NCI Surgery Branch has developed an experimental therapy that involves taking white blood cells from patients' tumors, growing them in the laboratory in large numbers, and then giving the cells back to the patient. These cells are called Tumor Infiltrating Lymphocytes, or TIL and we have given this type of treatment to over 200 patients with melanoma. Researchers want to know if TIL shrink s tumors in people with digestive tract, urothelial, breast, or ovarian/endometrial cancers. In this study, we are selecting a specific subset of white blood cells from the tumor that we think are the most effective in fighting tumors and will use only these cells in making the tumor fighting cells. Objective: The purpose of this study is to see if these specifically selected tumor fighting cells can cause digestive tract, urothelial, breast, or ovarian/endometrial tumors to shrink and to see if this treatment is safe. Eligibility: \- Adults age 18-72 with upper or lower gastrointestinal, hepatobiliary, genitourinary, breast, ovarian/endometrial cancer, or glioblastoma refractory to standard chemotherapy. Design: Work up stage: Patients will be seen as an outpatient at the NIH clinical Center and undergo a history and physical examination, scans, x-rays, lab tests, and other tests as needed. Surgery: If the patients meet all of the requirements for the study they will undergo surgery to remove a tumor that can be used to grow the TIL product. Leukapheresis: Patients may undergo leukapheresis to obtain additional white blood cells. (Leukapheresis is a common procedure, which removes only the white blood cells from the patient.) Treatment: Once their cells have grown, the patients will be admitted to the hospital for the conditioning chemotherapy, the TIL cells and aldesleukin. They will stay in the hospital for about 4 weeks for the treatment. Follow up: Patients will return to the clinic for a physical exam, review of side effects, lab tests, and scans about every 1-3 months for the first year, and then every 6 months to 1 year as long as their tumors are shrinking. Follow up visits will take up to 2 days. ...

Participants needed: 332
Trial details
Phase: Phase 2Age: 18-72Biological sex: AllType: InterventionalSponsor: National Cancer Institute (NCI)Updated: Aug 19, 2026Locations: 1
Eligibility criteria

Measurable (per RECIST v1.0 criteria), metastatic cancer of one of the following... [+22]

Participants who are pregnant or nursing because of the potentially dangerous ef... [+13]

Status: Recruiting

Phase 1 Study to Assess Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Antitumor Activity of ARR-002 in Advanced or Metastatic Ovarian or Endometrial Cancer.

This is a Phase 1 study to assess safety, tolerability, pharmacokinetics, immunogenicity, and antitumor activity of ARR-002 in advanced or metastatic ovarian or endometrial cancer.

Participants needed: 180
Trial details
Phase: Phase 1Age: 18+Biological sex: FemaleType: InterventionalSponsor: ArriVent BioPharma, Inc.Updated: Aug 10, 2026Locations: 2
Eligibility criteria

Patients with histologically and cytologically confirmed advanced or metastatic... [+6]

Prior treatment with auristatin-derived drugs s (eg, MMAE and monomethyl aurista... [+16]

Status: Not yet recruiting

Sacituzumab Tirumotecan +/- Pembrolizumab in I/O Exposed Metastatic or Recurrent Ovarian Clear Cell Cancer

This is a phase II randomized study of Sacituzumab tirumotecan, an intravenous antibody-drug conjugate (ADC) that targets Trop-1, administered alone or in combination with pembrolizumab, a monoclonal antibody to PD-1 in patients with relapsed clear cell cancers that originated in the ovary, fallopian tube or peritoneal cavity, inclusive of endometriosis (collectively referred to as OCCC throughout the protocol) after previous treatment with anti-PD1 therapy.

Participants needed: 50
Trial details
Phase: Phase 2Age: 18+Biological sex: FemaleType: InterventionalSponsor: Tufts Medical CenterUpdated: Jul 22, 2026Locations: 1
Eligibility criteria

Has a histologically-confirmed diagnosis of pure OCCC. Patients with mixed histo... [+18]

Has a history of documented severe dry eye syndrome, severe Meibomian gland dise... [+20]

Status: Recruiting

A Phase 1 Trial of ERX-315 in Participants With Advanced Solid Tumors

This is a Phase 1 study to assess the safety of ERX-315 in patients with advanced solid tumors that have failed approved systemic therapies.

Participants needed: 36
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: EtiraRx Australia Pty LtdUpdated: May 29, 2026Locations: 5
Eligibility criteria

Patients must be at least 18 years of age at the time of signing the informed co... [+5]

Systemic anti cancer therapy within 4 weeks of first dose of study drug [+3]

Status: Recruiting

Measuring Oncological Value of Exercise and Statin

The aim of the study is to find out whether supervised physical exercise during cancer drug treatment improves the effectiveness of the treatment in metastasized breast, kidney, ovarian and prostate cancer compared to unsupervised exercise. In addition, the investigators are investigating whether the use of atorvastatin combined with guided group exercise training would further improve the response to cancer treatment.

Participants needed: 240
Trial details
Phase: Phase 3Age: 18-99Biological sex: AllType: InterventionalSponsor: Tampere University HospitalUpdated: Jun 27, 2025Locations: 1
Eligibility criteria

The patient has metastatic prostate cancer, breast cancer, ovarian cancer or kid... [+7]

High risk of bone fractures [+12]