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. 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
  2. PROton Therapy for Post Surgical Treatment of GYNecologic Cancer

    This is a single institution, multi-center, Phase II, single-arm study, using Whole Pelvis (WP) Pencil Beam Scanning Proton Radiation (PBS PRT) in the post-surgical, adjuvant setting for definitive treatment of gynecologic cancers. The purpose of this study is to estimate rate of acute clinician-re…

    Stage
    Phase 2
    Ages
    18 and older
    Site
    Virtua Health, Voorhees Township, New Jersey
    Locations
    3 in total
    Run by
    Abramson Cancer Center at Penn Medicine
  3. Pembrolizumab and Lenvatinib in Advanced Cervical Cancer

    This is a phase II trial of combination therapy of pembrolizumab and lenvatinib in patients with locally advanced or metastatic cervical cancer that had failed first line of therapy. The hypothesis is the combination of lenvatinib and pembrolizumab will overcome vascular endothelial growth factor (…

    Stage
    Phase 2
    Ages
    18 and older
    Site
    MedStar Georgetown University Hospital, Washington D.C., District of Columbia
    Locations
    4 in total
    Run by
    Georgetown University
  4. A Study of STRO-004 in Adults With Refractory/Recurrent Metastatic Cancer

    This is a study to evaluate the safety and preliminary anti-tumor activity of STRO-004 in adults with metastatic cancer. This study includes 3 parts: * Part 1A is a dose escalation study of STRO-004 monotherapy in selected tumor types known to commonly express Tissue Factor (TF). * Part 1B is a coh…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    UC San Diego Moores Cancer Center, San Diego, California
    Locations
    9 in total
    Run by
    Sutro Biopharma, Inc.
  5. Hypofractionated External Beam Radiotherapy With Adaptive Planning for Endometrial and Cervical Cancers

    After surgery to remove the main endometrial and/or cervical tumor, most women receive radiation therapy. This study uses hypo-fractionated radiation therapy, which is a type of radiation therapy in which the total prescribed dose of radiation is delivered in fewer but larger doses than conventiona…

    Stage
    Not phased
    Ages
    18 and older
    Site
    University of California at Los Angeles, Los Angeles, California
    Run by
    Jonsson Comprehensive Cancer Center
  6. Dosing Physical Activity Among Older Cancer Survivors Who Experience Chronic Pain: a Micro-randomized Trial

    The purpose of this study is to assess the best time to deliver a message to increase physical activity and how often participants will experience a pain episode in the 24 hours following their receipt of a message to increase physical activity.

    Stage
    Not phased
    Ages
    65 and older
    Site
    Froedtert Hospital, Milwaukee, Wisconsin
    Run by
    Medical College of Wisconsin
  7. Evaluation of a Novel Optical Microscope With a Deep Depth of Field (DeepDOF) to Provide Histologic-quality Images on Cervical Biopsies and Loop Electrosurgical Excision Procedure (LEEP) Specimens at the Point-of-care

    All patients will be enrolled in Mozambique and Brazil. They will provide informed consent to use their cervical biopsy and/or LEEP specimens for imaging with DeepDOF prior to sending for standard of care processing and interpretation.

    Stage
    Not phased
    Ages
    25 to 49
    Site
    The University of Texas M. D. Anderson Cancer Center, Houston, Texas
    Run by
    M.D. Anderson Cancer Center
  8. A Phase 1 Study of NRM-823 in Participants With Locally Advanced or Metastatic Refractory Solid Tumors

    This study is being done to find out of NRM-823 is safe and can treat participants with locally advanced or metastatic solid tumors.

    Stage
    Phase 1
    Ages
    18 and older
    Site
    Normunity Investigational Site, Denver, Colorado
    Locations
    18 in total
    Run by
    Normunity AccelCo, Inc.
  9. A Study of BMS-986340 as Monotherapy and as Combination Therapy in Participants With Advanced Solid Tumors

    The purpose of this study is to assess the safety, tolerability, and recommended dose(s) of BMS-986340 as monotherapy and in combination with nivolumab, docetaxel, or Pumitamig in participants with advanced solid tumors. This study is a first-in-human (FIH) study of BMS-986340 in participants with …

    Stage
    Phase 1
    Ages
    18 and older
    Site
    Community Cancer Institute, Clovis, California
    Locations
    47 in total
    Run by
    Bristol-Myers Squibb
  10. MicroEnvironment Tumor Effects of Radiotherapy - Comprehensive Radiobiology Assessment TRial

    This study is a dynamically adjustable prospective longitudinal study designed to capture biospecimen (biopsy, blood, surgical) and multimodal treatment-related data (imaging, dosimetry, clinical) before, during, and after treatment with definitive-intent chemoradiotherapy for patients with locally…

    Stage
    Not phased
    Ages
    18 and older
    Site
    Washington University School of Medicine, St Louis, Missouri
    Run by
    Washington University School of Medicine
  11. PopSci CHW4CervixHealth

    Phase I: Validating self-collection kit by comparing their results with clinical Pap smear results in a cohort of 20 patients. Phase II: Evaluate the feasibility and acceptability of the CHW4CervicalHealth: Use of a self-collection kit to improve cervical health screening intervention aimed to prom…

    Stage
    Not phased
    Ages
    25 to 65
    Site
    Thomas Jefferson University, Philadelphia, Pennsylvania
    Run by
    Thomas Jefferson University
  12. Rice Technologies for Cervical Cancer Screening and Diagnosis

    The study aims to compare the accuracy of the lateral flow test to detect HPV at the POC with commercially available HPV test and to determine the diagnostic accuracy and reliability of a multimodal optical imaging system to detect cervical dysplasia, with the gold reference standard of histopathol…

    Stage
    Not phased
    Ages
    25 to 49
    Site
    M D Anderson Cancer Center, Houston, Texas
    Locations
    4 in total
    Run by
    M.D. Anderson Cancer Center
  13. 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
  14. 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
  15. 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
  16. 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
  17. 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
  18. 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
  19. 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
  20. 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
  21. 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
  22. 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
  23. 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
  24. 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
  25. 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

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.