Head and Neck Cancer Clinical Trials

101 studies are recruiting for head and neck 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. A First in Human Study of ALX2004 With Advanced or Metastatic Selected Solid Tumors

    A Phase 1, First in Human, Open-Label Multicenter Study to Evaluate ALX2004, an Antibody Drug Conjugate Targeting EGFR in Participants with Advanced or Metastatic Select Solid Tumors

    Stage
    Phase 1
    Ages
    18 and older
    Site
    ALX Center 9, La Jolla, California
    Locations
    12 in total
    Run by
    ALX Oncology Inc.
  2. Pilot Study of Management of Facial Paralysis in the Oncologic Patient: Nerve Transfer Techniques to Improve Facial Function and Quality of Life

    The goal of this research study is to measure changes in patients' quality of life after surgeries that affect the facial nerve, including nerve transfer as treatment for facial paralysis.

    Stage
    Not phased
    Ages
    18 and older
    Site
    The University of Texas M. D. Anderson Cancer Center, Houston, Texas
    Run by
    M.D. Anderson Cancer Center
  3. 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
  4. Intratumoral Delivery of Viral Replicon (saRNA) Particles Expressing IL-12 in Head and Neck Cancer

    The goal of this clinical trial is to assess the safety and tolerability of a virus replicon particle (VRP) encapsulated saRNA encoding IL-12 when injected into in head and neck cancer patients. The main questions being addressed are: The safety and tolerability of intratumoral (IT) injections of V…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    Stanford University, Stanford, California
    Run by
    VLP Therapeutics
  5. A Pilot Study of Ultra-High Dose Rate (ConformalFLASH®), for Reirradiation of Carcinoma of the Head and Neck

    This pilot study is designed to evaluate the feasibility of delivering ultra-high dose-rate conformal proton therapy (ConformalFLASH) in participants requiring re-irradiation for head and neck cancer who are not amenable to surgical resection. ConformalFLASH treatment planning and delivery workflow…

    Stage
    Not phased
    Ages
    18 and older
    Site
    The University of Pennsylvania, Department of Radiation Oncology, Philadelphia, Pennsylvania
    Run by
    IBA Proton Therapy, Inc.
  6. Postoperative Radiotherapy for Intermediate- and High-risk Patients With HNSCC Greater Than 6 Weeks After Surgery

    The goal of this clinical trial is to determine whether accelerated radiotherapy (involving 6 treatments per week) is better than standard radiotherapy (involving 5 treatments per week) at treating cancer of the head and neck when initiated more than 6 weeks after surgery.

    Stage
    Not phased
    Ages
    18 and older
    Site
    Levine Cancer Institute, Charlotte, North Carolina
    Locations
    3 in total
    Run by
    Wake Forest University Health Sciences
  7. A Study of [225Ac]Ac-AKY-1189 in Patients With Solid Tumors

    This is a first-in-human Phase 1b, 2-part, multicenter open-label clinical study to evaluate safety and efficacy of a Nectin-4 radiopharmaceutical ([225Ac]Ac-AKY-1189) in patients with locally advanced or metastatic solid tumors and to establish the maximum tolerated dose (MTD) or maximum administe…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    City of Hope, Duarte, California
    Locations
    14 in total
    Run by
    Aktis Oncology, Inc.
  8. Autologous CAR-T Cells Targeting CSPG4 in Relapsed/Refractory HNSCC

    The purpose of this study is to test the safety and tolerability of using a new treatment called autologous T lymphocyte chimeric antigen receptor cells against the CSPG4 antigen (iC9.CAR-CSPG4 T cells) in patients with head and neck cancer that came back after receiving standard therapy for this c…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    Lineberger Comprehensive Cancer Center at University of North Carolina Chapel Hill, Chapel Hill, North Carolina
    Run by
    UNC Lineberger Comprehensive Cancer Center
  9. Fatigue and Molecular Mechanisms in Cancer Patients Receiving CCRT

    Cancer-related fatigue (CRF) is a significant problem for cancer patients. This prospective, basic science, observational study will evaluate for changes in CRF associated with molecular characteristics prior to, during, and at the completion of non-investigational, standard-of-care, combined chemo…

    Stage
    Not phased
    Ages
    18 and older
    Site
    University of California, San Francisco, San Francisco, California
    Run by
    University of California, San Francisco
  10. Effects of Infusion Timing on Treatment Response in Solid Tumors

    This study evaluates whether the time of day when immunotherapy is given affects clinical outcomes. It includes patients eligible for PD-1 (programmed cell death protein 1) or PD-L1 (programmed death-ligand 1) inhibitor treatment who have either advanced or metastatic non-small cell lung cancer (NS…

    Stage
    Phase 2
    Ages
    18 and older
    Site
    University of North Carolina at Chapel Hill, Department of Radiation Oncology, Chapel Hill, North Carolina
    Run by
    UNC Lineberger Comprehensive Cancer Center
  11. Exercise and Nutritional Prehabilitation for Head and Neck Cancer Patients

    This study examines the acceptability, feasibility, and safety in developing a prehabilitation program for head and neck cancer patients. The purpose of this research is to access the safety and acceptability of using a prehabilitation program before head and neck cancer surgery.

    Stage
    Not phased
    Ages
    18 and older
    Site
    UC Davis Health, Sacramento, California
    Locations
    2 in total
    Run by
    University of California, Davis
  12. Building a Renewed ImaGe After Head & Neck Cancer Treatment (BRIGHT) Multi-Site RCT

    In this multi-center randomized clinical trial, head and neck cancer (HNC) survivors with clinically significant body image distress (BID) (N=180) will be randomized to BRIGHT (a brief video tele-cognitive behavioral therapy intervention) or Attention Control (AC, a manualized tele-supportive care …

    Stage
    Not phased
    Ages
    18 and older
    Site
    Henry Ford Hospital, Detroit, Michigan
    Locations
    5 in total
    Run by
    Medical University of South Carolina
  13. Atorvastatin to Reduce Cisplatin-Induced Hearing Loss Among Individuals With Head and Neck Cancer

    Background: Cisplatin is used to treat head and neck cancer. People who take this drug are at risk for hearing loss. Atorvastatin is a drug used to treat high cholesterol. It might reduce the risk of cisplatin-induced hearing loss. Objective: To find out if atorvastatin reduces hearing loss in peop…

    Stage
    Phase 2
    Ages
    18 to 100
    Site
    Winship Cancer Institute at Emory University, Atlanta, Georgia
    Locations
    5 in total
    Run by
    National Institute on Deafness and Other Communication Disorders (NIDCD)
  14. Prehabilitation Protocol for Head and Neck Cancer Patients

    The purpose of this research is to help researchers understand the barriers, supports, and preferences for prehabilitation. Prehabilitation in this study means head and neck cancer patients will receive nutritional counseling sessions and attend exercise programs before and during radiotherapy/chem…

    Stage
    Not phased
    Ages
    18 to 80
    Site
    University of Miami, Miami, Florida
    Run by
    University of Miami
  15. Home-based Respiratory Muscle Training for Minimizing Side Effects in Patients Undergoing Treatment for Cancer

    This clinical trial evaluates whether home-based respiratory muscle training is useful for minimizing side effects in patients undergoing treatment for cancer. Over-activation of the nervous system during breast cancer treatment can result in heart- and lung-related side effects which have the pote…

    Stage
    Not phased
    Ages
    21 and older
    Site
    Roswell Park Cancer Institute, Buffalo, New York
    Run by
    Roswell Park Cancer Institute
  16. A Study of Decreasing Radiation Therapy and Chemotherapy in People With Head and Neck Cancer

    The purpose of this study is to test the treatment approach of de-escalated radiation and chemotherapy followed by a planned neck dissection surgery in people with head and neck cancer. The study will look at how effective the treatment approach is against participants' cancer.

    Stage
    Phase 2
    Ages
    18 and older
    Site
    Memorial Sloan Kettering at Basking Ridge (Limited Protocol Activities), Basking Ridge, New Jersey
    Locations
    6 in total
    Run by
    Memorial Sloan Kettering Cancer Center
  17. Immunobiology Blood and Tissue Collection of Upper Aerodigestive Malignancies

    This research is being done to collect and store biological specimens (biospecimens) from people with cancer, regardless of tumor type, who are receiving treatments known or thought to have an effect on the immune system. The goal of this discovery and exploratory study is to: * Understand changes …

    Stage
    Not phased
    Ages
    18 and older
    Site
    Johns Hopkins University, Baltimore, Maryland
    Run by
    Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
  18. Antibiotic Treatment Effects on Intratumoral Bacteria Modulation in Surgical Patients With Oral Cancer

    The goal of this phase II single arm clinical study is to evaluate the effect of antibiotics (metronidazole) and oral chlorhexidine (CHX) in reducing the bacteria load within tumors of patients undergoing surgery for oral cancer.

    Stage
    Phase 2
    Ages
    18 and older
    Site
    Case Comprehensive Cancer Center, Cleveland Clinic Foundation, Cleveland, Ohio
    Run by
    Case Comprehensive Cancer Center
  19. Tongue Proactive Strengthening Exercise Program Following Partial/Hemi Glossectomy and Reconstruction

    This study is being done to determine whether adding a proactive tongue strengthening exercise program using a biofeedback device (the Tongueometer) improves speech and swallowing outcomes after surgery for tongue cancer. Patients who undergo partial or hemiglossectomy often experience difficulties…

    Stage
    Not phased
    Ages
    18 and older
    Site
    Case Comprehensive Cancer Center, Cleveland Clinic Foundation, Cleveland, Ohio
    Run by
    Case Comprehensive Cancer Center
  20. Novel Hypoxia Imaging for Head and Neck Cancer: Imaging Phenotype for Personalized Treatment

    Tumor hypoxia is one of the physiological factors for treatment resistance and likely contributes to poor overall survival among patients with head and neck cancer (HNC). Identifying hypoxic features of HNC may allow the personalizing treatment plan. The investigators propose multiparametric Hypoxi…

    Stage
    Not phased
    Ages
    18 and older
    Site
    University of Utah, Salt Lake City, Utah
    Run by
    University of Utah
  21. Reflectance Confocal Microscopy of Oral Cancers in Vivo: a Preliminary Trial Comparing Intra-oral Imaging With Pathology

    The purpose of this study is to get images (pictures) of oral lesions, which occur inside the mouth, before the patient's surgery using a special camera. These pictures will be used in our research to evaluate a new technology that uses a laser and takes pictures of the microscopic structure of tis…

    Stage
    Not phased
    Ages
    18 and older
    Site
    Memorial Sloan Kettering Basking Ridge (consent only), Basking Ridge, New Jersey
    Locations
    5 in total
    Run by
    Memorial Sloan Kettering Cancer Center
  22. Study of INBRX-106 and INBRX-106 in Combination With Pembrolizumab (Keytruda®) in Subjects With Locally Advanced or Metastatic Solid Tumors (Hexavalent OX40 Agonist)

    This is a Phase 1/2, open-label, non-randomized, 4-part trial to determine the safety profile and identify the maximum tolerated dose (MTD) and/or recommended Phase 2 dose (RP2D) of INBRX 106 administered as a single agent or in combination with the anti-PD-1 checkpoint inhibitor (CPI) pembrolizuma…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    City of Hope, Duarte, California
    Locations
    42 in total
    Run by
    Inhibrx Biosciences, Inc
  23. A Study of Cemiplimab With Chemotherapy and Immunotherapy in People With Head and Neck Cancer

    The purpose of this study is to find out whether combining the standard chemotherapy for head and neck cancer with the immunotherapy drugs cetuximab and cemiplimab (the study drug) is a safe treatment for head and neck cancer, and whether receiving this combination treatment before surgery may allo…

    Stage
    Phase 1
    Ages
    18 and older
    Site
    Memorial Sloan Kettering Basking Ridge (Limited Protocol Activities), Basking Ridge, New Jersey
    Locations
    7 in total
    Run by
    Memorial Sloan Kettering Cancer Center
  24. Jump: MR Simulation For Radiation Therapy Master Protocol

    This is a master protocol for a prospective Phase I-II study evaluating feasibility and efficacy of incorporating magnetic resonance imaging (MRI) simulation into the planning of radiation treatments.

    Stage
    Not phased
    Ages
    18 and older
    Site
    Brigham and Women Hospital, Boston, Massachusetts
    Locations
    2 in total
    Run by
    Brigham and Women's Hospital
  25. A Study Comparing Two Immunotherapy Options for Human Papillomavirus Positive HPV-Positive Head and Neck Cancer After Treatment

    The goal of this clinical trial is to learn if the combination of cemiplimab and fianlimab can improve outcomes compared to cemiplimab alone in adults with Human Papillomavirus Positive HPV-positive head and neck cancer who have detectable minimal-residual disease after definitive treatment. The ma…

    Stage
    Phase 2
    Ages
    18 and older
    Site
    The University of Chicago, Chicago, Illinois
    Run by
    University of Chicago

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.