Clinical Trials for Ovarian Cancer

Currently registered clinical trials for Ovarian Cancer from ClinicalTrials.gov. 27 recruiting, 50 total studies.

This content is for informational purposes only. Always consult a healthcare professional.

Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).

This page lists clinical trials related to Ovarian Cancer from the ClinicalTrials.gov database.

Trial Summary

  • Total studies: 50
  • Recruiting: 27
  • Active, not recruiting: 12
  • Completed: 3
  • Other: 8

Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.

Recruiting Trials

NCT01174121 — Immunotherapy Using Tumor Infiltrating Lymphocytes for Patients With Metastatic Cancer

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment332
Study TypeINTERVENTIONAL
ConditionsMetastatic Colorectal Cancer; Metastatic Pancreatic Cancer; Metastatic Ovarian Cancer; Metastatic Breast Carcinoma; Metastatic Endocrine Tumors/ Neuroendocrine Tumors
Interventions; ;

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 i…

StatusRecruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment1500
Study TypeOBSERVATIONAL
ConditionsPleuropulmonary Blastoma; Cystic Nephroma; Ovarian Sertoli-Leydig Cell Tumors; Ocular Medulloepithelioma; Nasal Chondromesenchymal Hamartoma

Background:

- Pleuropulmonary blastoma (PPB) is a rare fast-growing lung tumor that is associated with other, rare tumor types. Most cases of PPB appear in children younger than 6 years of age. Recently, it has been shown that this condition can be inherited (e.g., mutation of the DICER1 gene). Researchers are studying both clinical and genetic aspects of this newly described condition. They …

NCT03049462 — The Physiological Responses and Adaptation of Brown Adipose Tissue to Chronic Treatment With Beta3-Adrenergic Receptor Agonists

StatusRecruiting
PhasePhase 1
SponsorNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Enrollment100
Study TypeINTERVENTIONAL
ConditionsPolycystic Ovary Syndrome
Interventions;

Background:

Brown adipose tissue (BAT) is a type of fat in the body. It may prevent weight gain, improve insulin sensitivity, and reduce fatty liver. Researchers want to see if BAT helps the body burn energy.

Objective:

To learn more about how BAT works to burn energy.

Eligibility:

People ages 18-40 with a body mass index between 18 and 40

Design:

Participants will be screened with:

Med…

NCT04633239 — Testing the Addition of Abemaciclib to Olaparib for Women With Recurrent Ovarian Cancer

StatusRecruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment42
Study TypeINTERVENTIONAL
ConditionsRecurrent Ovarian High Grade Serous Adenocarcinoma; Recurrent Platinum-Resistant Ovarian Carcinoma
Interventions; ;

This phase I/Ib trial identifies the side effects and best dose of abemaciclib when given together with olaparib in treating patients with ovarian cancer that responds at first to treatment with drugs that contain the metal platinum but then comes back within a certain period (recurrent platinum-resistant). Abemaciclib may stop the growth of tumor cells by blocking some of the enzymes needed fo…

NCT05053230 — A Study Evaluating the Integrative Medicine at Home (IM@HOME) Program in People With Cancer

StatusRecruiting
PhaseN/A
SponsorMemorial Sloan Kettering Cancer Center
Enrollment324
Study TypeINTERVENTIONAL
ConditionsHead and Neck Cancer; Head and Neck Tumor; Thoracic Tumor; Thoracic Cancer; Gynecologic Cancer
Interventions;

The overarching long-term goal of the Integrative Medicine for Patient-reported Outcomes Values and Experience (IMPROVE) research program is to evaluate whether integrating a virtual mind-body programming, Integrative Medicine at Home (IM@Home), will improve patient perceived values, outcomes, and experiences as they undergo systemic cancer treatment such as chemotherapy, immunotherapy, radioth…

NCT04847063 — Individual Response to Hyperthermic Intraperitoneal Chemotherapy (HIPEC) Treatment of Peritoneal Carcinomatosis From Peritoneal Mesothelioma or Atypical Mesothelial Proliferation or From Ovarian, Colorectal, or Appendiceal Histologies

StatusRecruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment60
Study TypeINTERVENTIONAL
ConditionsPeritoneal Mesothelioma; Peritoneal Carcinomatosis; Ovarian Cancer; Gastrointestinal Cancer; Appendiceal Cancer
Interventions; ;

Background:

Cytoreductive surgery (CRS) removes tumors in the abdomen. HIPEC is hyperthermic (heated) chemotherapy that washes the inside of the abdomen. CRS with HIPEC may help people with peritoneal carcinomatosis. These are tumors that have spread to the lining of the abdomen from other cancers. Researchers think they can improve the results of CRS with HIPEC treatment on these tumors by ch…

NCT05417594 — Study of AZD9574 as Monotherapy and in Combination With Anti-cancer Agents in Participants With Advanced Solid Malignancies

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorAstraZeneca
Enrollment695
Study TypeINTERVENTIONAL
ConditionsAdvanced Solid Malignancies
Interventions; ;

This study will assess the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary efficacy of AZD9574 individually and in combination with anti-cancer agents in participants with advanced cancer that has recurred/progressed.

NCT05564377 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Locally Advanced or Advanced Solid Tumors, The ComboMATCH Screening Trial

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment2900
Study TypeINTERVENTIONAL
ConditionsAdvanced Malignant Solid Neoplasm; Anatomic Stage III Breast Cancer AJCC v8; Anatomic Stage IV Breast Cancer AJCC v8; Locally Advanced Malignant Solid Neoplasm; Malignant Female Reproductive System Neoplasm
Interventions; ;

This ComboMATCH patient screening trial is the gateway to a coordinated set of clinical trials to study cancer treatment directed by genetic testing. Patients with solid tumors that have spread to nearby tissue or lymph nodes (locally advanced) or have spread to other places in the body (advanced) and have progressed on at least one line of standard systemic therapy or have no standard treatmen…

NCT05768139 — First-in-Human Study of Tersolisib (STX-478) as Monotherapy and in Combination With Other Antineoplastic Agents in Participants With Advanced Solid Tumors

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorEli Lilly and Company
Enrollment880
Study TypeINTERVENTIONAL
ConditionsBreast Cancer; Solid Tumors, Adult
Interventions; ;

Study STX-478-101 (LY4064809) is a multipart, open-label, phase 1/2 study evaluating the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of STX-478 (LY4064809) in participants with advanced solid tumors with P13Ka mutations.

Part 1 will evaluate STX-478 as monotherapy in participants with advanced solid tumors. Part 2 will evaluate STX-478 therapy as combination…

NCT05554328 — Testing the Use of the Combination of Selumetinib and Olaparib or Selumetinib Alone Targeted Treatment for RAS Pathway Mutant Recurrent or Persistent Ovarian and Endometrial Cancers, A ComboMATCH Treatment Trial

StatusRecruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment165
Study TypeINTERVENTIONAL
ConditionsRecurrent Endometrial Carcinoma; Recurrent Fallopian Tube Carcinoma; Recurrent Ovarian Carcinoma; Recurrent Primary Peritoneal Carcinoma
Interventions; ;

This phase II ComboMATCH treatment trial compares selumetinib plus olaparib to selumetinib alone in women with endometrial or ovarian (fallopian tube and primary peritoneal) cancer that has come back (recurrent) or that remains despite treatment (persistent) and harbors a mutation in the RAS pathway. Selumetinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell …

NCT05950464 — Testing Different Amounts of the Combination of Drugs M1774 and ZEN-3694 for the Treatment of Recurrent Ovarian and Endometrial Cancer

StatusRecruiting
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment65
Study TypeINTERVENTIONAL
ConditionsRecurrent Endometrial Carcinoma; Recurrent Endometrial Clear Cell Adenocarcinoma; Recurrent Endometrial Endometrioid Adenocarcinoma; Recurrent Endometrial Low Grade Endometrioid Adenocarcinoma; Recurrent Ovarian Clear Cell Adenocarcinoma
Interventions; ;

This phase Ib trial tests the safety, side effects, and best dose of M1774 when given with ZEN-3694 in treating patients with ovarian and endometrial cancer that has come back (recurrent). M1774 and ZEN-3694 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. M1774 and ZEN-3694 combined together has demonstrated to be better than either drug alone in killi…

NCT05942300 — CPI-0209 Plus Carboplatin in Patients With Platinum Sensitive Recurrent Ovarian Cancer

StatusRecruiting
PhasePhase 1
SponsorLan Coffman
Enrollment30
Study TypeINTERVENTIONAL
ConditionsRecurrent Ovarian Cancer
Interventions;

This is a clinical trial using CPI-0209 in combination with Carboplatin chemotherapy followed by CPI-0209 maintenance in patients with platinum sensitive, recurrent ovarian cancer.

NCT06465069 — A Study of LY4052031 in Participants With Advanced or Metastatic Urothelial Cancer or Other Solid Tumors

StatusRecruiting
PhasePhase 1
SponsorEli Lilly and Company
Enrollment420
Study TypeINTERVENTIONAL
ConditionsMetastatic Solid Tumor; Recurrent Solid Tumor; Advanced Solid Tumor; Urinary Bladder Neoplasm; Triple Negative Breast Cancer
Interventions

The purpose of this study is to find out whether the study drug, LY4052031, is safe, tolerable and effective in participants with advanced, or metastatic solid tumors including urothelial cancer. The study is conducted in two parts - phase Ia (dose-escalation, dose-optimization) and phase Ib (dose-expansion). The study will last up to approximately 4 years.

NCT06760819 — A Study to Learn More About How Well Treatment With Sevabertinib (BAY 2927088) Tablets Works and How Safe it is in Participants Who Have a Solid Tumor With Mutations of the Human Epidermal Growth Factor Receptor 2 (HER2)

StatusRecruiting
PhasePhase 2
SponsorBayer
Enrollment111
Study TypeINTERVENTIONAL
ConditionsAdvanced Solid Tumors; HER2 Mutation
Interventions

Researchers are looking for a better way to treat people who have solid tumors with HER2-activating mutations. Before a treatment can be approved for people to take, researchers do clinical trials to better understand its safety and how it works.

In this trial, the researchers want to learn how well BAY2927088 (sevabertinib) works in people with different types of solid tumors with HER2 mutati…

NCT06799065 — First-in-Human Study of ATX-295, an Oral Inhibitor of KIF18A, in Patients With Advanced or Metastatic Solid Tumors, Including Ovarian Cancer

StatusRecruiting
PhasePhase 1
SponsorAccent Therapeutics
Enrollment90
Study TypeINTERVENTIONAL
ConditionsAdvanced Solid Tumors; Breast Cancer Recurrent; Ovarian Cancer; High-grade Serous Ovarian Carcinoma; Triple Negative Breast Cancer
Interventions

The goal of this study is to identify a safe and tolerated dose of the orally administered KIF18A inhibitor ATX-295. In addition, this study will evaluate the pharmacokinetics, pharmacodynamics and preliminary antitumor activity of ATX-295 in patients with advanced solid tumors and ovarian cancer.

NCT06995898 — The Vanguard Study: Testing a New Way to Screen for Cancer

StatusRecruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment24000
Study TypeINTERVENTIONAL
ConditionsBladder Carcinoma; Breast Carcinoma; Colorectal Carcinoma; Esophageal Carcinoma; Gastric Carcinoma
Interventions; ;

The Vanguard Study is a feasibility study to explore several aspects of evaluating multi-cancer detection (MCD) tests in a future definitive randomized controlled trial. An MCD test measures markers in the blood in order to screen for multiple cancers simultaneously. There is a need to understand how MCDs may work as cancer screening tools. The goal of cancer screening is to reduce the burden o…

NCT07070726 — UNTOLD Ovarian Cancer Unmet Needs Survey

StatusRecruiting
PhaseN/A
SponsorMasonic Cancer Center, University of Minnesota
Enrollment2000
Study TypeOBSERVATIONAL
ConditionsOvarian Cancer

The goal of this study is to comprehensively measure ongoing concerns and unmet needs of individuals living with ovarian cancer. To accomplish this, the UNderstanding The experience of Ovarian cancer - Life after Diagnosis (UNTOLD) study will be conducted using a mixed-methods approach. Ovarian cancer survivors will be enrolled to participate in UNTOLD to complete a one-time survey regarding th…

NCT07115043 — A Study to Investigate Safety of AZD6750 in Adult Participants With Select Advanced or Metastatic Solid Tumors

StatusRecruiting
PhasePhase 1 / Phase 2
SponsorAstraZeneca
Enrollment60
Study TypeINTERVENTIONAL
ConditionsMelanoma; Non-small Cell Lung Cancer; Squamous Cell Carcinoma (Skin); Renal Cell Carcinoma; Merkel Cell Carcinoma
Interventions;

A Study to Investigate Safety of AZD6750 in Adult Participants With Select Advanced or Metastatic Solid Tumors

NCT07213791 — A Study of LY4337713 in Participants With FAP-Positive Solid Tumors

StatusRecruiting
PhasePhase 1
SponsorEli Lilly and Company
Enrollment241
Study TypeINTERVENTIONAL
ConditionsOvarian Neoplasms; Breast Neoplasms; Pancreatic Intraductal Neoplasms; Colorectal Neoplasms; Esophageal Neoplasms
Interventions

This is a study of LY4337713 in participants with certain types of cancer that is advanced or has spread. Participants must have cancer with high levels of a protein called fibroblast activation protein (FAP). The purpose of this study is to evaluate safety, side effects, and efficacy of LY4337713. In addition, this study will evaluate how much LY4337713 gets into the bloodstream, how it is bro…

NCT07213804 — A Three-Part Phase 3 Study of Sofetabart Mipitecan in Participants With Platinum-Resistant (Part A) and Platinum-Sensitive (Parts B and C) Ovarian Cancer

StatusRecruiting
PhasePhase 3
SponsorEli Lilly and Company
Enrollment1630
Study TypeINTERVENTIONAL
ConditionsOvarian Neoplasms; Fallopian Tube Neoplasms; Peritoneal Neoplasms; Neoplasm Metastasis
Interventions; ;

This is a clinical study that has three parts. It is testing a potential new medicine called Sofetabart Mipitecan (Sofe-M) for people with certain types of ovarian, peritoneal, and fallopian tube cancers. Part A enrolls participants with platinum-resistant cancer, meaning their disease progressed during or within six months of platinum-based chemotherapy. Parts B and C enroll participants with …

NCT07402915 — Drug-drug Interaction Study With AZD5335 and Itraconazole in Participants With Ovarian, Primary Peritoneal, or Fallopian Tube Cancer

StatusRecruiting
PhasePhase 1
SponsorAstraZeneca
Enrollment24
Study TypeINTERVENTIONAL
ConditionsFallopian Tube Cancer; Ovarian Cancer; Primary Peritoneal
Interventions;

The purpose of this study is to assess the effect of itraconazole on the pharmacokinetics (PK) of AZ14170132.

NCT07306559 — A Study to Test How Well Different Doses of BI 3820768 Are Tolerated by People With Advanced Cancer (Solid Tumours)

StatusRecruiting
PhasePhase 1
SponsorBoehringer Ingelheim
Enrollment187
Study TypeINTERVENTIONAL
ConditionsAdvanced Relapsed or Refractory Germ Cell Tumours; Advanced Relapsed or Refractory Endometrial Cancer; Advanced Relapsed or Refractory Ovarian Cancer
Interventions

This study is open to adults with advanced germ cell tumours, endometrial cancer, or ovarian cancer whose previous treatments were not successful. People can join the study if they have no remaining treatment options or if standard therapy is not suitable. The purpose of this study is to test increasing doses of BI 3820768 to find a dose that people with these types of cancer can tolerate and t…

NCT07460752 — Evaluation of Alternative Site Goserelin Acetate Injection for Ovarian Function Suppression (OFS) in Local and Locally Advanced Premenopausal Hormone Receptor Positive Breast Cancer Patients

StatusRecruiting
PhasePhase 2
SponsorMayo Clinic
Enrollment98
Study TypeINTERVENTIONAL
ConditionsAnatomic Stage I Breast Cancer AJCC v8; Anatomic Stage II Breast Cancer AJCC v8; Anatomic Stage III Breast Cancer AJCC v8; Locally Advanced Hormone Receptor-Positive Breast Carcinoma
Interventions; ;

This phase II trial determines if giving goserelin acetate injections in the upper gluteal region is as effective for ovarian function suppression (OFS) as giving injections in the abdomen for ovarian function suppression (OFS) in premenopausal patients with hormone receptor positive breast cancer that has not spread to other parts of the body (localized) or that has spread to nearby tissue or …

NCT07286266 — A Study to Investigate Mocertatug Rezetecan Compared With Standard of Care in Participants With Platinum-resistant Ovarian Cancer (BEHOLD-Ovarian01)

StatusRecruiting
PhasePhase 3
SponsorGlaxoSmithKline
Enrollment450
Study TypeINTERVENTIONAL
ConditionsOvarian Neoplasms
Interventions; ;

This study specifically aims to evaluate how well mocertatug rezetecan (Mo-Rez) works in treating ovarian cancer compared to standard treatments. The study also assesses whether Mo-Rez is safe and tolerated well by participants compared to standard treatments and aims to provide a better understanding of the main side effects of the drug.

NCT07690189 — Phase 1 Study of NTB-928 in R/R OC

StatusRecruiting
PhasePhase 1
SponsorTeneoSeven, Inc.
Enrollment90
Study TypeINTERVENTIONAL
ConditionsRelapsed/Refractory Ovarian Carcinoma
Interventions

The goal of this clinical trial is to determine if NTB-928 can be given safely to adult females with ovarian cancer that has come back (relapsed) or stopped responding to treatment (refractory), how NTB-928 moves through the body, and how the immune system reacts to it. The study will also look for early signs of anti-cancer activity of NTB-928. The main questions the study aims to answer are: …

NCT07686783 — Ovarian Reserve After Laparoscopic Cystectomy for Endometriotic and Non-Endometriotic Cysts

StatusRecruiting
PhaseN/A
SponsorBenha University
Enrollment60
Study TypeINTERVENTIONAL
ConditionsOvarian Cysts; Endometriosis; Benign Ovarian Cyst; Ovarian Reserve; Cystectomy
Interventions

We will conduct this study to estimate the effect of laparoscopic cystectomy on ovarian reserve in endometriotic cysts versus non-endometriotic cysts.

NCT07665515 — Study of CryptiVax-1001 in Maintenance Setting for Advanced Serous Ovarian, Fallopian Tube, or Primary Peritoneal Cancer

StatusRecruiting
PhasePhase 1
SponsorEpitopea Ltd
Enrollment50
Study TypeINTERVENTIONAL
ConditionsOvarian Cancer; HGSOC; HGS Ovarian, Fallopian Tube or Primary Peritoneal Cancer
Interventions

Ovarian, fallopian tube, or primary peritoneal cancer, collectively referred to as ovarian cancer, remains the deadliest type of gynaecological cancer. The most common and aggressive form is called high-grade serous ovarian cancer.

The main purpose of this study is to understand whether an experimental study vaccine, CryptiVax-1001, is safe when administered to patients with high-grade serous …

Active, Not Recruiting

NCT00339495 — Prostate Lung Colorectal and Ovarian (PLCO) Cancer Screening Trial

StatusActive, not recruiting
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment154900
Study TypeOBSERVATIONAL
ConditionsCancer; Death

The Division of Cancer Preventionl (DCP, formerly DCPC), under extramural contracts to 10 U.S. clinical centers, is evaluating the effectiveness of screening for prostate, lung, colorectal and ovarian cancer (The PLCO Trial). In 1996 the NCI Executive Committee approved the expansion of the PLCO Trial to collect additional materials and to conduct additional studies. About, 74,000 men and 74,00…

NCT01081262 — Carboplatin and Paclitaxel or Oxaliplatin and Capecitabine With or Without Bevacizumab as First-Line Therapy in Treating Patients With Newly Diagnosed Stage II-IV or Recurrent Stage I Epithelial Ovarian or Fallopian Tube Cancer

StatusActive, not recruiting
PhasePhase 3
SponsorNational Cancer Institute (NCI)
Enrollment50
Study TypeINTERVENTIONAL
ConditionsBorderline Ovarian Mucinous Tumor; Ovarian Mucinous Cystadenocarcinoma; Recurrent Fallopian Tube Carcinoma; Recurrent Ovarian Carcinoma; Stage IA Fallopian Tube Cancer AJCC v6 and v7
Interventions; ;

This randomized phase III trial studies carboplatin given together with paclitaxel with or without bevacizumab to see how well it works compared with oxaliplatin given together with capecitabine with or without bevacizumab as first-line therapy in treating patients with newly diagnosed stage II-IV, or recurrent (has come back) stage I epithelial ovarian or fallopian tube cancer. Drugs used in c…

NCT02068794 — MV-NIS Infected Mesenchymal Stem Cells in Treating Recurrent Ovarian, Primary Peritoneal or Fallopian Tube Cancer

StatusActive, not recruiting
PhasePhase 1 / Phase 2
SponsorMayo Clinic
Enrollment34
Study TypeINTERVENTIONAL
ConditionsFallopian Tube Clear Cell Adenocarcinoma; Fallopian Tube Endometrioid Adenocarcinoma; Fallopian Tube Mucinous Adenocarcinoma; Fallopian Tube Serous Adenocarcinoma; Fallopian Tube Transitional Cell Carcinoma
Interventions; ;

This phase I/II trial studies the side effects and best dose of oncolytic measles virus encoding thyroidal sodium iodide symporter (MV-NIS) infected mesenchymal stem cells and to see how well it works in treating patients with ovarian, primary peritoneal or fallopian tube cancer that has come back. Mesenchymal stem cells may be able to carry tumor-killing substances directly to ovarian, primary…

NCT01883297 — “Re-Stimulated” TILs And IL-2 Therapy for Platinum Resistant Ovarian, Fallopian Tube, or Primary Peritoneal Cancer

StatusActive, not recruiting
PhasePhase 1
SponsorUniversity Health Network, Toronto
Enrollment3
Study TypeINTERVENTIONAL
ConditionsRecurrent; Platinum-resistant; High Grade Serous Ovarian Cancer; Fallopian Tube Cancer; Primary Peritoneal Cancer
Interventions; ;

This is a phase I clinical study for patients with platinum-resistant high grade serous ovarian, fallopian tube, or primary peritoneal cancer, and the response to a combination of cyclophosphamide, autologous tumor-infiltrating lymphocytes (TILs), autologous dendritic cells (DCs), and OKT3 (anti-CD3 antibody), along with low-dose interleukin-2 (IL-2) therapy.

NCT02484404 — Phase I/II Study of the Anti-Programmed Death Ligand-1 Durvalumab Antibody (MEDI4736) in Combination With Olaparib and/or Cediranib for Advanced Solid Tumors and Advanced or Recurrent Ovarian, Triple Negative Breast, Lung, Prostate and Colorectal Can…

StatusActive, not recruiting
PhasePhase 1 / Phase 2
SponsorNational Cancer Institute (NCI)
Enrollment268
Study TypeINTERVENTIONAL
ConditionsColorectal Neoplasms; Breast Neoplasms
Interventions; ;

Background:

- Durvalumab is a drug that may help people s immune systems respond to and kill cancer cells. Olaparib is a drug that may inhibit repairing DNA damage of cancer cells. Cediranib is a drug that may stop the blood vessel growth of cancer cells. This study has two components. In the phase 1 component of the study, researchers want to investigate how well participants tolerate the co…

NCT02465060 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial)

StatusActive, not recruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment6452
Study TypeINTERVENTIONAL
ConditionsAdvanced Lymphoma; Advanced Malignant Solid Neoplasm; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma
Interventions; ;

This phase II MATCH screening and multi-sub-trial studies how well treatment that is directed by genetic testing works in patients with solid tumors, lymphomas, or multiple myelomas that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) and does not respond to treatment (refractory). Patients must have progressed following at leas…

NCT02650986 — Gene-Modified T Cells With or Without Decitabine in Treating Patients With Advanced Malignancies Expressing NY-ESO-1

StatusActive, not recruiting
PhasePhase 1 / Phase 2
SponsorRoswell Park Cancer Institute
Enrollment15
Study TypeINTERVENTIONAL
ConditionsAdvanced Fallopian Tube Carcinoma; Advanced Malignant Solid Neoplasm; Advanced Melanoma; Advanced Ovarian Carcinoma; Advanced Primary Peritoneal Carcinoma
Interventions; ;

This phase I/IIa trial studies the side effects and best dose of gene-modified T cells when given with or without decitabine, and to see how well they work in treating patients with malignancies expressing cancer-testis antigens 1 (NY-ESO-1) gene that have spread to other places in the body (advanced). A T cell is a type of immune cell that can recognize and kill abnormal cells of the body. Pla…

NCT03587311 — Bevacizumab and Anetumab Ravtansine or Paclitaxel in Treating Patients With Refractory Ovarian, Fallopian Tube, or Primary Peritoneal Cancer

StatusActive, not recruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment96
Study TypeINTERVENTIONAL
ConditionsFallopian Tube Endometrioid Adenocarcinoma; Fallopian Tube High Grade Serous Adenocarcinoma; Ovarian Endometrioid Adenocarcinoma; Ovarian High Grade Serous Adenocarcinoma; Platinum-Resistant Fallopian Tube Carcinoma
Interventions; ;

This phase II trial studies the side effects of bevacizumab and anetumab ravtansine or paclitaxel in treating patients with ovarian, fallopian tube, or primary peritoneal cancer that does not respond to treatment (refractory). Bevacizumab is a monoclonal antibody that may interfere with the ability of tumor cells to grow and spread. Anetumab ravtansine is a drug that targets a protein in the bo…

NCT03737643 — Durvalumab Treatment in Combination With Chemotherapy and Bevacizumab, Followed by Maintenance Durvalumab, Bevacizumab and Olaparib Treatment in Advanced Ovarian Cancer Patients

StatusActive, not recruiting
PhasePhase 3
SponsorAstraZeneca
Enrollment1407
Study TypeINTERVENTIONAL
ConditionsAdvanced Ovarian Cancer
Interventions; ;

This is a Phase III randomised, double-blind, multi-centre study to evaluate the efficacy and safety of durvalumab in combination with standard of care platinum based chemotherapy and bevacizumab followed by maintenance durvalumab and bevacizumab or durvalumab, bevacizumab and olaparib in patients with newly diagnosed advanced ovarian cancer.

NCT04739800 — Comparison of Standard of Care Treatment With a Triplet Combination of Targeted Immunotherapeutic Agents

StatusActive, not recruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment120
Study TypeINTERVENTIONAL
ConditionsFallopian Tube Mucinous Adenocarcinoma; Ovarian Seromucinous Carcinoma; Platinum-Refractory Fallopian Tube Carcinoma; Platinum-Refractory Ovarian Carcinoma; Platinum-Refractory Primary Peritoneal Carcinoma
Interventions; ;

This phase II trial studies the possible benefits of treatment with different combinations of the drugs durvalumab, olaparib and cediranib vs. the usual treatment in patients with ovarian, primary peritoneal, or fallopian tube cancer that has come back after a period of improvement with platinum therapy (recurrent platinum resistant). Usual treatment is the type of treatment most patients with …

NCT05715216 — EON: A Single-arm Phase II Study of Etigilimab (OMP-313M32) in Combination With Checkpoint Inhibition (Nivolumab) in Patients With Platinum-resistant, Recurrent Epithelial Ovarian Cancer

StatusActive, not recruiting
PhasePhase 2
SponsorM.D. Anderson Cancer Center
Enrollment23
Study TypeINTERVENTIONAL
ConditionsOvarian Cancer
Interventions;

To learn if adding etigilimab to nivolumab therapy can help to control clear cell ovarian, fallopian tube, and primary peritoneal cancers that are resistant to platinum-based therapy

NCT06619236 — Study to Assess the Efficacy of Rina-S Compared to Treatment of Investigator’s Choice in Participants With Platinum Resistant Ovarian Cancer

StatusActive, not recruiting
PhasePhase 3
SponsorGenmab
Enrollment530
Study TypeINTERVENTIONAL
ConditionsPlatinum-resistant Ovarian Cancer
Interventions; ;

This phase 3 study will be conducted in different countries all over the world.

The purpose of this study is to compare how well Rina-S works against platinum-resistant ovarian cancer compared to chemotherapy drugs that are already approved and used for platinum-resistant ovarian cancer.

Treatment in this study could be Rina-S or it could be 1 of 4 indicated chemotherapy agents that are consi…

Not Yet Recruiting

NCT07604766 — An Extension Study to Assess the Efficacy of Rina-S Compared to Treatment of Investigator’s Choice in Participants With Platinum Resistant Ovarian Cancer in China

StatusNot yet recruiting
PhasePhase 3
SponsorGenmab
Enrollment82
Study TypeINTERVENTIONAL
ConditionsPlatinum-resistant Ovarian Cancer
Interventions; ;

The purpose of this Chinese extension study is to compare how well Rina-S works against platinum-resistant ovarian cancer compared to chemotherapy drugs that are already approved and used for platinum-resistant ovarian cancer.

Treatment in this study could be Rina-S or it could be 1 of 4 indicated chemotherapy agents that are considered standard medical care. There is an equal (50:50) chance o…

NCT07687602 — A Study to Evaluate Adverse Events and Change in Disease Activity of Mirvetuximab Soravtansine-gynx in Adults With Folate Receptor-Alpha Positive, Platinum-Resistant Ovarian Cancer in a Real-World Setting

StatusNot yet recruiting
PhaseN/A
SponsorAbbVie
Enrollment69
Study TypeOBSERVATIONAL
ConditionsFolate Receptor-Alpha Positive Platinum-Resistant High-Grade Serous Epithelial Ovarian Cancer; Folate Receptor-Alpha Positive Platinum-Resistant Fallopian Tube Cancer; Folate Receptor-Alpha Positive Platinum-Resistant Primary Peritoneal Cancer

Epithelial ovarian cancer, which includes fallopian tube and primary peritoneal cancers, is a lethal disease with 3,221 new cases reported in 2021 in Korea. The purpose of this study is to evaluate the adverse events and change in disease activity of mirvetuximab soravtansine-gynx (MIRV) in participants with folate receptor-alpha (FRα) positive, platinum-resistant, high-grade serous epithelial …

NCT07687667 — Effects of GLP-1RAs on Fertility Outcomes in Obese Women With PCOS

StatusNot yet recruiting
PhaseN/A
SponsorPeking University Third Hospital
Enrollment406
Study TypeINTERVENTIONAL
ConditionsPolycystic Ovary Syndrome (PCOS); Obesity; Infertility, Female
Interventions;

The goal of this clinical trial is to examine whether GLP1-RA and healthy lifestyle education in women with PCOS and obesity prior to fertility treatment improves live birth rate and other reproductive, maternal and perinatal outcomes compared to metformin plus healthy lifestyle education.

NCT07564141 — Study to Assess the Efficacy and Safety of Rina-S With or Without Bevacizumab Compared to Investigator’s Choice of Platinum-based Chemotherapy With or Without Bevacizumab as Second-line Treatment in Participants With Recurrent Platinum-sensitive Ovarian Cancer

StatusNot yet recruiting
PhasePhase 3
SponsorGenmab
Enrollment688
Study TypeINTERVENTIONAL
ConditionsPlatinum-Sensitive Ovarian Cancer; Ovarian Cancer
Interventions; ;

This Phase 3 study will be conducted in different countries around the world with up to about 688 participants.

The purpose of this study is to evaluate how well Rina-S works against ovarian cancer in combination with or without bevacizumab and how it compares to an investigator’s choice of platinum-based chemotherapy with or without bevacizumab.

Participants will receive either:

  • Rina-S mo…

NCT07690332 — A Real-World Study of Mirvetuximab Soravtansine (MIRV) in Ovarian Cancer Patients of Expression of Folate Receptor α

StatusNot yet recruiting
PhaseN/A
SponsorNING LI-GYN
Enrollment400
Study TypeOBSERVATIONAL
ConditionsOvarian Cancer; Fallopian Tube Cancers; Primary Peritoneal Cancer
Interventions

Mirvetuximab soravtansine (MIRV) is an antibody-drug conjugate approved for the treatment of ovarian cancer. However, real-world data on its safety and effectiveness in routine clinical practice are limited, especially in the Chinese patient population. MIRAS is a multicenter, prospective,observational, real-word study of Mirvetuximab Soravtansine in patients of Advanced Ovarian Cancer, Fallopi…

NCT07504588 — Sacituzumab Govitecan With Bevacizumab Compared to Usual Chemotherapy (Carboplatin, Pegylated Liposomal Doxorubicin and Bevacizumab) for Treating Recurrent Platinum-Sensitive Ovarian Cancer After PARP Inhibitor Maintenance Therapy

StatusNot yet recruiting
PhasePhase 2
SponsorNational Cancer Institute (NCI)
Enrollment87
Study TypeINTERVENTIONAL
ConditionsRecurrent Platinum-Sensitive Fallopian Tube Endometrioid Adenocarcinoma; Recurrent Platinum-Sensitive Fallopian Tube High Grade Serous Adenocarcinoma; Recurrent Platinum-Sensitive Ovarian High Grade Endometrioid Adenocarcinoma; Recurrent Platinum-Sensitive Ovarian High Grade Serous Adenocarcinoma; Recurrent Platinum-Sensitive Primary Peritoneal Endometrioid Adenocarcinoma
Interventions; ;

This phase II trial compares the effect of sacituzumab govitecan and bevacizumab to standard care (carboplatin, pegylated liposomal doxorubicin, and bevacizumab) in patients with ovarian cancer that has come back after an initial response to platinum therapy (platinum-sensitive), that has progressed after poly (adenosine diphosphate-ribose) polymerase (PARP) inhibitor maintenance therapy (recur…

Completed Trials

NCT00040222 — Clinical, Genetic, Behavioral, Laboratory and Epidemiologic Characterization of Individuals and Families at High Risk of Breast/Ovarian Cancer

StatusCompleted
PhaseN/A
SponsorNational Cancer Institute (NCI)
Enrollment377
Study TypeOBSERVATIONAL
ConditionsFamilial Ovarian Cancer; Familial Breast Cancer; BRCA1-associate Malignancies; BRCA2-associated Malignancies

Individuals and families with known or suspected syndromes that include breast, ovarian or genetically-related cancers are enrolled in this family study, which is a syndrome-specific sub-set of the long-standing DCEG Human Genetics Program umbrella family studies protocol (78-C-0039). Cancer outcomes are documented through review of medical, vital, and pathology records. Selected individuals an…

NCT01352962 — Gemcitabine, Carboplatin, and Lenalidomide for Treatment of Advanced/Metastatic Urothelial Cancer and Other Solid Tumors

StatusCompleted
PhasePhase 1
SponsorNational Cancer Institute (NCI)
Enrollment18
Study TypeINTERVENTIONAL
ConditionsUrethral Neoplasms; Neoplasms, Urethral; Cancer of the Urethra; Urethral Cancer
Interventions; ;

Background:

- Gemcitabine and carboplatin are chemotherapy drugs used to treat several types of cancer, including cancer of the pancreas, bladder, ovaries, and lung. Lenalidomide, a drug that prevents the growth of new blood vessels in tumors, has been approved for treatment of certain blood cancers, but it has not yet been approved for use in combination with gemcitabine and carboplatin. Res…

NCT04560452 — Drug Intensive Monitoring Study of Olaparib in Clinical Practice Among Chinese Patients

StatusCompleted
PhaseN/A
SponsorAstraZeneca
Enrollment1018
Study TypeOBSERVATIONAL
ConditionsOvarian Cancer; Prostate Cancer

This is a multi-centre, prospective, non-interventional study. The study will enrol about 860 Chinese cancer patients from around 56 sites. For OC cohort, the subjects who had received olaparib for at least one dose before study enrolment in real world practices will be enrolled ( n=800) . For PC cohort, according to the doctor’s decision, patients who have prescribed and agreed to start taking…

Other (Withdrawn)

NCT02432378 — Intensive Locoregional Chemoimmunotherapy for Recurrent Ovarian Cancer Plus Intranodal DC Vaccines

StatusWithdrawn
PhasePhase 1 / Phase 2
SponsorRoswell Park Cancer Institute
EnrollmentN/A
Study TypeINTERVENTIONAL
ConditionsCancer of Ovary; Cancer of the Ovary; Neoplasms, Ovarian; Ovarian Cancer; Ovary Cancer
Interventions;

This study will evaluate the immunologic and potential clinical effectiveness of intensive locoregional sequential intraperitoneal (IP) cisplatin (IPC) with intravenous (iv) paclitaxel followed by peritoneal infusion of a chemokine modulatory (CKM) regimen composed of a cocktail of IP rintatolimod and interferon-alpha (IFNα) for patients with advanced stage ovarian cancer (III-IV) at primary ne…

Other (Terminated)

NCT06466187 — A Study of SGN-MesoC2 in Advanced Solid Tumors

StatusTerminated
PhasePhase 1
SponsorSeagen, a wholly owned subsidiary of Pfizer
Enrollment19
Study TypeINTERVENTIONAL
ConditionsCarcinoma, Non-Small-Cell Lung; Ovarian Neoplasms; Pancreatic Adenocarcinoma; Colorectal Neoplasms; Mesothelioma
Interventions

This clinical trial is studying advanced solid tumors. Solid tumors are cancers that start in a part of your body like your lungs or liver instead of your blood. Once tumors have grown bigger in one place but haven’t spread, they’re called locally advanced. If your cancer has spread to other parts of your body, it’s called metastatic. When a cancer has gotten so big it can’t easily be removed o…