Ovarian Cancer Clinical Trials
153 studies are recruiting for ovarian cancer in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies, page 3
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A Study of PHST001 in Advanced Solid Tumors
This is a multi-center, first-in-human (FIH), open-label, Phase 1a/1b dose escalation and dose expansion study to assess the safety, PK, pharmacodynamics, and antitumor activity of PHST001 monotherapy (Phase 1a) or in combination with anticancer therapies (Phase 1b) in adult participants with advan…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Precision NextGen Oncology & Research Center, Beverly Hills, California
- Locations
- 20 in total
- Run by
- Pheast Therapeutics
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The Evaluation of PC14586 in Patients With Advanced Solid Tumors Harboring a TP53 Y220C Mutation (PYNNACLE)
The Phase 2 monotherapy portion of this study is currently enrolling and will evaluate the efficacy and safety of PC14586 (INN rezatapopt) in participants with locally advanced or metastatic solid tumors harboring a TP53 Y220C mutation. The Phase 1 portion of the study will assess the safety, toler…
- Stage
- Phase 1
- Ages
- 12 and older
- Site
- University of San Diego Moores Cancer Center, La Jolla, California
- Locations
- 76 in total
- Run by
- PMV Pharmaceuticals, Inc
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Distance-Based Exercise to Preserve Function and Prevent Disability
This clinical trial studies whether an exercise program can be successfully delivered to patients receiving treatment for cancer through virtual sessions and allow patients to exercise in their own home. Treatments for cancer can cause side effects such as fatigue and loss of strength. These side e…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Kaiser Permanente Dublin, Dublin, California
- Locations
- 23 in total
- Run by
- Alliance for Clinical Trials in Oncology
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177Lu-BetaBart in Patients With Relapsed/Refractory, Locally Advanced Inoperable, or Metastatic Solid Tumors
This is a Phase 1/2a dose escalation and expansion study to determine the safety, tolerability, and preliminary clinical activity of 177LuBetaBart, a lutetium-labeled anti-B7-H3 monoclonal antibody, in patients with relapsed/refractory, locally advanced inoperable, or metastatic solid tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Dothan Hematology & Oncology, Dothan, Alabama
- Locations
- 5 in total
- Run by
- Radiopharm Theranostics, Ltd
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A Phase 1, First-in-Human (FIH), Open-Label, Dose-Escalation and Dose Expansion Study of the Peptide Drug Conjugate (PDC), TS-104, as a Monotherapy in Subjects With Select Advanced Solid Tumors
A Phase 1, First-in-Human (FIH), Open-Label, Dose-Escalation and Dose Expansion Study of the Peptide Drug Conjugate (PDC), TS-104, as a Monotherapy in Subjects with Select Advanced Solid Tumors. The main goals of this study are to: * Find the recommended dose of TS-104 that can safely be given to p…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Site 06, Maumee, Ohio
- Locations
- 3 in total
- Run by
- TwoStep Therapeutics, Inc.
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Leveraging Methylated DNA Markers (MDMs) in the Detection of Endometrial Cancer, Ovarian Cancer, and Cervical Cancer
The overarching objective of this project is to develop a pan-gynecologic cancer detection test using gynecologic (unique endometrial, cervical, and ovarian cancer) cancer-specific methylated DNA markers and high-risk human papilloma virus (HR-HPV) detected in vaginal fluid and/or plasma. This prop…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Mayo Clinic, Phoenix, Arizona
- Locations
- 25 in total
- Run by
- Mayo Clinic
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A Study of NT-175 in Adult Participants With Advanced Malignancies That Are Positive for HLA-A*02:01 and the TP53 R175H Mutation
Phase I Study of NT-175, an autologous T cell therapy product genetically engineered to express an HLA-A*02:01-restricted T cell receptor (TCR), targeting TP53 R175H mutant malignancies
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Research Site, Gilbert, Arizona
- Locations
- 20 in total
- Run by
- AstraZeneca
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DESTINY-PANTUMOUR04
This study will evaluate the effectiveness of T-DXd in patients with HER2-positive (IHC 3+) locally advanced, unresectable, or metastatic solid tumors who have received prior systemic treatment for metastatic or advanced disease and have no satisfactory alternative treatment options in a real-world…
- Stage
- Not phased
- Ages
- 18 to 130
- Site
- Research Site, Birmingham, Alabama
- Locations
- 18 in total
- Run by
- AstraZeneca
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A Study to Find Out How Safe REGN5668 is and How Well it Works In Adult Women When Given With Either Cemiplimab, or Cemiplimab + Fianlimab, or Ubamatamab
This study is researching an investigational drug called REGN5668 : * alone or, * combined with cemiplimab (also known as REGN2810) or, * combined with both cemiplimab and fianlimab (also known as REGN3767), or * combined with ubamatamab (also known as REGN4018), with or without sarilumab. The main…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- City of Hope Comprehensive Cancer Center, Duarte, California
- Locations
- 28 in total
- Run by
- Regeneron Pharmaceuticals
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Study of Dato-DXd as Monotherapy and in Combination With Anti-cancer Agents in Patients With Advanced Solid Tumours (TROPION-PanTumor03)
TROPION-PanTumor03 will investigate the safety, tolerability, and anti-tumour activity of Datopotamab Deruxtecan (Dato-DXd) as Monotherapy and in Combination with Anticancer Agents in Patients with Advanced/Metastatic Solid Tumours.
- Stage
- Phase 2
- Ages
- 18 to 130
- Site
- Research Site, Los Angeles, California
- Locations
- 96 in total
- Run by
- AstraZeneca
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Evaluate BL-B01D1 in Patients With Metastatic or Unresectable Non-Small Cell Lung Cancer (NSCLC) and Other Solid Tumors
The objective of this study is to evaluate the safety, tolerability, and efficacy of BL-B01D1 in patients with Metastatic or Unresectable Non-Small Cell Lung Cancer (NSCLC) and Other Solid Tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Beverly Hills Cancer Center, Beverly Hills, California
- Locations
- 37 in total
- Run by
- SystImmune Inc.
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Prehabilitation in High-risk Oncologic Surgery
The goal of this clinical study is to learn whether a prehabilitation program can improve recovery after major abdominal surgery in adults with cancer who are receiving treatment before surgery. Prehabilitation is supportive care given before surgery to help patients prepare physically, nutritional…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Fox Chase Cancer Center - Philadelphia, Philadelphia, Pennsylvania
- Run by
- Fox Chase Cancer Center
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Prospective Laboratory Study Biologic Specimens and Tumor Tissue of Patients With Cancer
Ascites samples from women undergoing surgery for ovarian cancer will be collected for use in translational research.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of New Mexico Cancer Center, Albuquerque, New Mexico
- Run by
- New Mexico Cancer Research Alliance
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Fecal Microbiota Transplantation in Treating Immune-Checkpoint Inhibitor Induced-Diarrhea or Colitis in Genitourinary Cancer Patients
This trial studies how well fecal microbiota transplantation works in treating diarrhea or colitis (inflammation of the intestines) that is caused by certain types of medications (called immune-checkpoint inhibitors) in patients with genitourinary cancer. Fecal microbiota transplantation may effect…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- M D Anderson Cancer Center, Houston, Texas
- Run by
- M.D. Anderson Cancer Center
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BI-1808 as a Single Agent and With Pembrolizumab (KEYTRUDA® ) in Treatment of Advanced Malignancies(Keynote-D20)
The goal of this first in human clinical trial is to test BI-1808 administered as single agent and in combination with pembrolizumab in subjects with advanced malignancies whose disease has progressed after standard therapy. The main questions it aims to answer are: * how safe and tolerable is BI-1…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- City of Hope National Medical Center, Duarte, California
- Locations
- 25 in total
- Run by
- BioInvent International AB
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Infusion of Autologous T Cells Engineered to Target FSH Receptor in Recurrent Ovarian Cancer
The purpose of this first in human study is to evaluate the safety of treatment with autologous T cells genetically modified to express a CER (chimeric endocrine receptor) targeting the FSHR (follicle-stimulating hormone receptor) (FSHCER T cells), with or without conditioning chemotherapy, in part…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Moffitt Cancer Center, Tampa, Florida
- Run by
- H. Lee Moffitt Cancer Center and Research Institute
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A Study of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer With Cyclin E1 Overexpression
This study will evaluate the safety and efficacy of INCB123667 in Participants With Platinum-Resistant Ovarian Cancer (PROC) With Cyclin E1 Overexpression.
- Stage
- Phase 2
- Ages
- 18 to 99
- Site
- Usa Health Mitchell Cancer Institute, Mobile, Alabama
- Locations
- 74 in total
- Run by
- Incyte Corporation
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A Study of Isoquercetin in People With Ovarian Cancer
The purpose of this study is to test whether isoquercetin can reduce markers in the blood that may indicate the risk of blood clots in people with ovarian cancer. The effects of isoquercetin will be compared with those of a placebo.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Memorial Sloan Kettering Basking Ridge (All Protocol Activities), Basking Ridge, New Jersey
- Locations
- 8 in total
- Run by
- Memorial Sloan Kettering Cancer Center
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Investigation of Ubamatamab Combination Therapy in Adult Participants With Platinum-Resistant Ovarian Cancer
This study is researching an experimental drug called ubamatamab, also referred to as "study drug". The study is focused on participants who have advanced ovarian cancer. The aim of the study is to see how safe, tolerable, and effective the study drug is on its own and in combination with other ant…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- The University of Alabama at Birmingham, Birmingham, Alabama
- Locations
- 56 in total
- Run by
- Regeneron Pharmaceuticals
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DT2216 + Paclitaxel in Platinum-Resistant Ovarian Cancer
The purpose of this research study is determining the highest dose of the study drug DT2216 in combination with paclitaxel that can be safely and tolerably administered in recurrent ovarian cancer. The names of the study drugs involved in this study are: * DT2216 (a type of proteolysis-targeting ch…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Beth Israel Deaconess Medical Center (BIDMC), Boston, Massachusetts
- Locations
- 3 in total
- Run by
- Elizabeth Stover, MD, PhD
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Clinical Trial of Autologous B7-H3 CAR T Cells in Reoccurent Platinum-resistant Ovarian Tumors
This is a single site, open label, Phase 1 study using a 3 + 3 dose escalation design in two cohorts of adults with recurrent, platinum-resistant ovarian tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Stanford University, Palo Alto, California
- Run by
- Stanford University
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Study of Psilocybin Assisted Psychotherapy to Address Fear of Recurrence
The goal of this clinical trial is to test whether psilocybin along with therapy in women with early breast cancer and ovarian cancer in remission can improve their fear of recurrence. The main question[s] it aims to answer [is/are]: Does psilocybin assisted therapy improve fear of cancer recurrenc…
- Stage
- Phase 1
- Ages
- 21 and older
- Site
- Outpatient CTRC, Aurora, Colorado
- Locations
- 2 in total
- Run by
- University of Colorado, Denver
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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.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institute at Florida Cancer Specialists, Orlando, Florida
- Locations
- 6 in total
- Run by
- ArriVent BioPharma, Inc.
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FT836 With or Without Chemotherapy and/or Monoclonal Antibodies, in Participants With Advanced Solid Tumors
This is a Phase 1 study of FT836 administered in participants with advanced solid tumors. The primary objectives of the study are to evaluate the safety and tolerability of FT836 with or without chemotherapy and/or trastuzumab or cetuximab, and to determine the recommended phase 2 dose (RP2D) of FT…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- UC San Diego Moores Cancer Center, La Jolla, California
- Locations
- 5 in total
- Run by
- Fate Therapeutics
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Study of TUB-040 Given With Standard Ovarian Cancer Drugs in Patients With Fast-growing Ovarian Cancer
The goal of this clinical study is to learn more about the safety, tolerability, and preliminary effectiveness of TUB-040 when given in combination with standard ovarian cancer treatments in participants with high-grade epithelial serous or endometrioid ovarian cancer. This study will also evaluate…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Start Cal, Los Angeles, California
- Locations
- 8 in total
- Run by
- Tubulis GmbH
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.