Phase 2 Head and Neck Cancer Trial, Recruiting NCT07178301 Sponsor: Northwestern University Condition: Head and Neck Cancer
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Phase 2 Head and Neck Cancer Trial, Recruiting

NCT07178301
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been diagnosed with a type of throat cancer (oropharyngeal squamous cell carcinoma) that is linked to the HPV virus, confirmed by a specific laboratory test called HPV in situ hybridization.
  • People who have not received any prior treatment for this cancer (such as chemotherapy given before the main treatment).
  • People whose cancer can be measured or evaluated using standard imaging criteria known as RECIST v1.1.
  • People who are 18 years of age or older.
  • People whose cancer is classified as Stage I or II (AJCC 8th edition), meaning the tumour falls within certain size and spread categories, and there is no evidence the cancer has spread to other parts of the body (confirmed by physical examination and a PET scan).
  • People who have had a PET scan to assess the stage of their cancer before joining the trial.
  • People who are generally well enough to carry out normal daily activities, with only minor limitations — rated 0 or 1 on a standard scale doctors use to measure overall health and activity level (ECOG Performance Status).
  • People who are planned to receive radiation therapy (RT) either alone or combined with chemotherapy, with chemotherapy decisions made by the treating doctor according to standard care.
  • People who are able to become pregnant must agree to use an adequate form of contraception (such as hormonal or barrier methods, surgical methods, or abstinence) from the time of consent and throughout the period of receiving radiation therapy.
  • People who are able to become pregnant must have a negative pregnancy test, or sign a standard declination form, before the planning CT scan for radiation therapy.
  • People who are able to understand the study information and are willing to sign a written consent form before joining the trial.

Who may not be able to join:

  • People whose cancer is classified at a more advanced stage — specifically T4, N3, or M1 under the AJCC 8th edition staging system — meaning the tumour is very large, has spread extensively to lymph nodes, or has spread to other parts of the body.
  • People who have previously had radiation therapy to the head or neck area in a way that would overlap with the radiation fields planned for this trial.
  • People who have had major surgery to the head or neck area that may have affected the flow of fluid through the lymphatic system, as determined by the lead investigator.
  • People who have an uncontrolled ongoing illness that could interfere with receiving radiation therapy, including uncontrolled connective tissue diseases (such as lupus or scleroderma), mental health or social circumstances that would make it difficult to follow the study requirements, or any other condition the treating doctor believes could affect safety or the ability to complete the study.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Laila A Gharzai, Northwestern University

Phone: 312-695-1301

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
5 December 2025
Est. completion
20 March 2030

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

2-year locoregional progression free survival

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov