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Search / Trial NCT05678348

Pyrimethamine as an Inhibitor of NRF2 in HPV-unrelated Locally Advanced Head and Neck Squamous Cell Carcinoma

Launched by WASHINGTON UNIVERSITY SCHOOL OF MEDICINE · Jan 4, 2023

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

Head And Neck Cancer Squamous Cell Carcinoma Nrf2 Pyrimethamine Treatment Resistance

ClinConnect Summary

This clinical trial is studying a medication called pyrimethamine to see if it can help treat a specific type of head and neck cancer. The researchers believe that pyrimethamine might slow down the growth of tumors by blocking a protein pathway that cancer cells use to survive and resist treatment. While pyrimethamine has been used for many years to treat infections, its effects on human tumors are not well understood, which is what this study aims to explore.

To be eligible for this trial, participants must be at least 18 years old and have been diagnosed with locally advanced (Stage III-IV) head and neck squamous cell carcinoma that is not related to the human papillomavirus (HPV). They should also be in good overall health with functioning bone marrow and organs. Participants will receive the study drug and may need to have a small biopsy of their tumor before starting treatment. It's important for anyone considering joining this trial to discuss it with their doctor, especially if they have any health conditions or are taking other medications.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Histologically or cytologically confirmed, locally advanced (Stage III-IV) head and neck squamous cell carcinoma (HNSCC) undergoing surgical-based treatment with curative intent that is HPV-unrelated disease, defined as SCC of the oral cavity, larynx, or hypopharynx, p16 negative SCC of the oropharynx.
  • At least 18 years of age.
  • ECOG performance status ≤ 1
  • * Normal bone marrow and organ function as defined below:
  • Leukocytes ≥ 3.0 K/cumm
  • Absolute neutrophil count ≥ 1.5 K/cumm
  • Platelets ≥ 100 K/cumm
  • Total bilirubin ≤ 1.5 x IULN
  • AST(SGOT)/ALT(SGPT) ≤ 3.0 x IULN
  • Creatinine clearance \> 50 mL/min by Cockcroft-Gault
  • Able to swallow study drug
  • The effects of pyrimethamine on the developing human fetus are unknown. For this reason and because it is in Pregnancy Category C, women of childbearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control, abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she must inform her treating physician immediately.
  • Ability to understand and willingness to sign an IRB approved written informed consent document.
  • Patient must be able to undergo a research biopsy prior to starting treatment, or have previously banked baseline tumor biopsy of at least 20 mg of frozen tissue collected under Tissue Acquisition Protocol (IRB 201102323).
  • Exclusion Criteria:
  • Prior therapy for this cancer.
  • A history of other malignancy with the exception of malignancies for which all treatment was completed at least 2 years before registration and the patient has no evidence of disease.
  • Prior treatment with pyrimethamine in the year prior to HNSCC diagnosis.
  • Currently receiving any other investigational agents.
  • A history of allergic reactions attributed to compounds of similar chemical or biologic composition to pyrimethamine or other agents used in the study.
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, current use of systemic immunosuppressive medications, symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia.
  • Documented megaloblastic anemia due to folate deficiency.
  • Treatment with anticoagulant or antiplatelet therapy in the year prior to HNSCC diagnosis.
  • Pregnant and/or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 7 days of Day 1.
  • Patients with HIV are eligible unless their CD4+ T-cell counts are \< 350 cells/mcL or they have a history of AIDS-defining opportunistic infection within the 12 months prior to registration. Concurrent treatment with effective ART according to DHHS treatment guidelines is recommended.
  • Active alcohol abuse in the opinion of the treating physician.
  • Currently taking phenytoin

About Washington University School Of Medicine

Washington University School of Medicine is a leading academic medical institution renowned for its commitment to advancing healthcare through innovative research, education, and patient care. With a strong emphasis on translating scientific discoveries into practical applications, the institution conducts a diverse array of clinical trials aimed at improving treatment outcomes and enhancing the understanding of various medical conditions. Its collaborative environment fosters partnerships between researchers, clinicians, and community stakeholders, ensuring that the trials not only contribute to scientific knowledge but also address the pressing health needs of diverse populations.

Locations

Saint Louis, Missouri, United States

Patients applied

0 patients applied

Trial Officials

Paul Zolkind, M.D.

Principal Investigator

Washington University School of Medicine

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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