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

  1. 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
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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.
  8. 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
  9. 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
  10. 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
  11. 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
  12. 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
  13. 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
  14. 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
  15. 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
  16. 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
  17. 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
  18. 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
  19. 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
  20. 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
  21. 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
  22. 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
  23. 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
  24. 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
  25. 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.