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
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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.
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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
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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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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
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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.
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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
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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.
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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
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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
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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
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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
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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
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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)
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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
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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.