Cervical Cancer Clinical Trials
75 studies are recruiting for cervical 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 2
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GCCC 2578 Randomized Photon vs Proton RT for Newly Diagnosed Gynecologic Primaries
The purpose of study is to compare the side effects of two different forms of radiation for endometrial and cervical cancer. If you decide to enroll in this study, you will be randomized to one of two treatment groups. This study will compare two standard of care treatments: "Conventional" pHoton r…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Maryland Proton Treatment Center, Baltimore, Maryland
- Locations
- 5 in total
- Run by
- University of Maryland, Baltimore
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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
- 18 in total
- Run by
- Alliance for Clinical Trials in Oncology
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A Trial of Robotic Versus Open Hysterectomy Surgery in Cervix Cancer
This is a randomized controlled trial to compare survival for patients who undergoe robotic assisted laparoscopy versus open hysterectomy and lymph node assessment for the treatment of early stage cervical cancer.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- City of Hope, Duarte, California
- Locations
- 156 in total
- Run by
- GOG Foundation
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A Study of Sacituzumab Govitecan (IMMU-132) in Patients With Recurrent or Persistent Cervical Cancer
This is a non-randomized Phase 2 study of sacituzumab govitecan (IMMU-132) in subjects with recurrent or persistent cervical cancer.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Smilow Cancer Hospital at Yale New Haven, New Haven, Connecticut
- Locations
- 2 in total
- Run by
- Yale University
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Feasibility of HPV Self-Collection Kits for Cervical Cancer Screening
This study is testing and implementing an equity-focused, community-based intervention that improves women's access to cervical cancer screening and adherence to follow up after an abnormal result. The study's objective is to assess and compare the feasibility of different methods of distributing a…
- Stage
- Not phased
- Ages
- 25 and older
- Site
- Washington University School of Medicine, St Louis, Missouri
- Run by
- Washington University School of Medicine
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Strategies to Close the Gap From Cervical Cancer Diagnosis to Treatment in Botswana
Investigators will test the effectiveness of adaptive strategies on timely adoption of cervical cancer treatment in Botswana using a pragmatic trial design.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Nyangabgwe Referral Hospital, Francistown, North-East District
- Locations
- 3 in total
- Run by
- Abramson Cancer Center at Penn Medicine
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Study of RGT-490 in Patients With PIK3CA-Mutated Advanced Solid Tumors
This is a phase 1/1b, open-label, multicenter study consisting of sequential parts designed to evaluate the safety, tolerability, and effects pharmacokinetic (PK) profile, and antitumor activity of RGT-490, an investigational oral therapy, in adults with locally advanced or metastatic solid tumors …
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- START Los Angeles, Los Angeles, California
- Locations
- 5 in total
- Run by
- Regor Pharmaceuticals Inc.
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Radiation Combined With BIspecific T-Cell Engager in DLL3 Expressing Tumors
Phase I study to examine safety of the addition of concurrent tarlatamab with standard palliative and consolidative RT regimens , with a main cohort of N=20-24 patients with extracranial anatomic radiation sites. I) After lead in of 10 patients demonstrating safety of treatment, allow for expansion…
- Stage
- Phase 1
- Ages
- 18 to 99
- Site
- Arizona Cancer Center at UMC North/University Medical Center, Tucson, Arizona
- Locations
- 2 in total
- Run by
- University of Arizona
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Trial of Single Protein Encapsulated Doxorubicin, SPEDOX-6 in Advanced Malignancies
This is a Phase 1b/IIa dose escalation clinical trial determining the recommended phase II dose of SPEDOX-6 in subjects with advanced, therapy-refractory soft-tissue sarcoma (STS); triple-negative breast cancer (TNBC); Non-small cell lung cancer (NSCLC); cervical cancer; ovarian cancer; KRAS mutant…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Chao Family Comprehensive Cancer Center University of California, Irvine, Orange, California
- Run by
- University of California, Irvine
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Navigation Intervention for Adolescent and Young Adult Cancer Survivors
The investigators propose to: 1) Adapt an evidence-based cancer-focused patient navigation (PN) program for the Adolescent and Young Adult (AYA) cancer survivor population; and 2) Plan and conduct an effectiveness-implementation trial of this program within Kaiser Permanente Southern California (KP…
- Stage
- Not phased
- Ages
- 21 to 45
- Site
- KP Southern California - Department of Research & Evaluation, Pasadena, California
- Run by
- Kaiser Permanente
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A Clinical Trial to Assess PVX7 Immunotherapy Regimens in Advanced Cervical Cancer Patients
A Feasibility Trial of PVX7 vaccine in advanced cervical cancer patients who have completed primary definitive therapy.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- The University of Alabama at Birmingham, Birmingham, Alabama
- Locations
- 2 in total
- Run by
- Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
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E7 T-cell Receptor (TCR) -T Cell Induction Therapy for Locoregionally Advanced HPV-associated Cancers
The goal of this study is to determine the feasibility of administration of a single dose of E7 TCR-T cells as induction therapy prior to definitive treatment (chemoradiation or surgery) of locoregionally advanced HPV-associated cancers. The intent of E7 TCR-T cell treatment is to shrink or elimina…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Rutgers Cancer Institute, New Brunswick, New Jersey
- Locations
- 2 in total
- Run by
- Christian Hinrichs
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E7 TCR-T Cell Immunotherapy for Human Papillomavirus (HPV) Associated Cancers
This is a phase II clinical trial to assess the clinical activity of immunotherapy with E7 TCR-T cells for metastatic HPV-associated cancers. HPV-associated cancers in include cervical, throat, penile, vulvar, vaginal, anal, and other cancers. Participants will receive a conditioning regimen, E7 TC…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- National Institutes of Health Clinical Center, Bethesda, Maryland
- Locations
- 3 in total
- Run by
- Christian Hinrichs
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Safety and Tolerability of ²¹²Pb-DOTAM-GRPR1 in Adult Subjects With Recurrent or Metastatic GRPR-expressing Tumors
A Phase 1 Open-Label, First-in-human, Dose Escalation and Expansion Study to Determine the Safety, Tolerability, Dosimetry, Pharmacokinetics, and Preliminary Efficacy of 212Pb-DOTAM-GRPR1 in Adult Participants with Recurrent or Metastatic GRPR-expressing Tumors
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- UK Markey Cancer Center, Lexington, Kentucky
- Locations
- 8 in total
- Run by
- Orano Med Theranostics, SAS
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Novel, One Stop, Affordable, Point of Care and AI Supported System of Screening, Triage and Treatment Selection for Cervical Cancer in LMICs
Artificial intelligence (AI) is fast gaining reputation as a highly promising solution for cervical cancer screening. AI-based detection of cervical neoplasias is named automated visual exam (AVE) by the National Cancer Institute, USA. The investigators propose to develop and evaluate the performan…
- Stage
- Not phased
- Ages
- 25 to 49
- Site
- University of Cincinnati, Cincinnati, Ohio
- Locations
- 2 in total
- Run by
- International Agency for Research on Cancer
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Physical Activity Intervention Among Older Women With Gynecologic Cancers (Fit4Treatment)
The primary purpose of the study is to determine which of four components (symptom-burden tailored app, exercise partner, oncology provider engagement, coaching) added to a core intervention of a wearable activity tracker and commercially available app, will improve physical activity. The findings …
- Stage
- Not phased
- Ages
- 60 and older
- Site
- Northwestern University, Chicago, Illinois
- Run by
- Northwestern University
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Blood and Urine HPVDNA as Minimally Invasive Biomarkers for Cervical Cancer Detection and Surveillance Following Treatment
The purpose of this study is to determine if ctHPVDNA (circulating tumor HPV DNA) can be used as a non-invasive biomarker for identification and treatment monitoring of cervical cancer by characterizing correlation between plasma ctHPVDNA, urine transrenal HPVDNA (TrHPVDNA) levels and presence of c…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Melissa Knutsen, Chapel Hill, North Carolina
- Locations
- 2 in total
- Run by
- UNC Lineberger Comprehensive Cancer Center
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Using Reiki Therapy to Improve Symptoms Associated With Brachytherapy in Patients With Gynecological Malignancies
The goal of this open label, randomized, controlled clinical trial is to assess the benefits of providing Reiki therapy to subjects receiving their first brachytherapy treatment for gynecological malignancies. Participants will either receive a session of Reiki therapy or usual care during the stan…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- Huntsman Cancer Institute, Salt Lake City, Utah
- Run by
- University of Utah
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Dose Escalation and Dose Expansion Study of MDX2001 in Patients With Advanced Solid Tumors
This study is designed to characterize the safety, tolerability, and anti-tumor activity of MDX2001 in patients with advanced solid tumors.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- Sarah Cannon Research Institute, Denver, Colorado
- Locations
- 6 in total
- Run by
- ModeX Therapeutics, An OPKO Health Company
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Study of Pembrolizumab and Lenvatinib in Metastatic and Recurrent Cervix Cancer (LenPem Cervix)
The main purpose of this study is to gather information about an investigational drug combination, Lenvatinib in combination with pembrolizumab, that may help to treat cervical cancers. In this study, we are looking to see whether the combination of lenvatinib and pembrolizumab has any effect on sl…
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- UT Southwestern Medical Center, Dallas, Texas
- Run by
- University of Texas Southwestern Medical Center
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PRGN-2009 in Combination With Pembrolizumab in Patients With Recurrent or Metastatic Cervical Cancer
This Phase 2 study will evaluate the efficacy and safety of PRGN-2009 in combination with pembrolizumab in patients with pembrolizumab-resistant recurrent or metastatic cervical cancer.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- University of Arkansas for Medical Sciences, Little Rock, Arkansas
- Locations
- 3 in total
- Run by
- Precigen, Inc
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Early Pelvic Floor Physical Therapy for Women Undergoing Pelvic Radiation for Gynecologic Malignancies
This is a single arm phase II study in which 28 patients who will be undergoing definitive pelvic external beam radiation therapy for cervical cancer will receive pelvic floor physical therapy 4 weeks after completing radiation therapy.
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Cincinnati, Cincinnati, Ohio
- Run by
- University of Cincinnati
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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
- 24 in total
- Run by
- Mayo Clinic
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Patient Preference for Subcutaneous vs. Intravenous Immune Therapy
The study will evaluate patient and Health Care Professional- reported preference for Subcutaneous (SC) compared with IV nivolumab administration or similarly for SC compared with IV pembrolizumab.
- Stage
- Phase 2
- Ages
- 18 and older
- Site
- UPMC Hillman Cancer Center, Pittsburgh, Pennsylvania
- Run by
- Diwakar Davar
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A Study of VET3-TGI in Patients With Solid Tumors
VET3-TGI is an oncolytic immunotherapy designed to treat advanced cancers. VET3-TGI has not been given to human patients yet, and the current study is designed to find a safe and effective dose of VET3-TGI when administered by direct injection into tumor(s) (called an intratumoral injection) or whe…
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- USC/Norris Comprehensive Cancer Center, Los Angeles, California
- Locations
- 7 in total
- Run by
- KaliVir Immunotherapeutics
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.