What this study is
Simplified from ClinicalTrials.govTesting two existing drugs, metformin (a diabetes medicine) or naproxen (a pain and inflammation medicine), to learn about their safety and side effects as a way to help prevent oral cancer in adults 18 and older with Fanconi anemia, an inherited condition that raises cancer risk.
Read the original summary from ClinicalTrials.gov
Finding effective ways to slow down or prevent the development of cancer in people with Fanconi anemia (FA) is a critical medical priority. Individuals with FA are at dramatically higher risk of developing aggressive cancers, particularly of the head and neck, and these cancers are difficult to treat with standard therapies such as surgery, chemotherapy or radiation. Because options for treatment are limited and outcomes are often poor, prevention strategies are urgently needed.
In this study, the investigators will test two widely available drugs, metformin and naproxen, to evaluate whether they can lower the risk of cancer in FA patients. Metformin is commonly prescribed for type 2 diabetes, while naproxen is a nonsteroidal anti-inflammatory drug (NSAID) frequently used for pain and inflammation. Both have shown potential in previous research to influence biological pathways linked to cancer development. By repurposing these well-known drugs, this trial aims to explore a safe, practical approach to cancer prevention in this vulnerable population.
The study, conducted at the Rockefeller University and the University of Minnesota, has several goals. First, the investigators will carefully assess the safety and tolerability of metformin and naproxen when used in participants with FA. Because these individuals can be more susceptible to metabolic disorders like diabetes compared to the general population, and may have genitourinary abnormalities related to their underlying condition, monitoring for side effects and adverse events is especially important. Second, investigators will evaluate whether intervention affects visible or microscopic changes in the mouth, where cancers often arise. This will involve performing small biopsies of oral tissue to look for cancerous or pre-cancerous lesions. Third, investigators will investigate early molecular changes using an exploratory less invasive technique: collecting cells with a soft brush, similar to a toothbrush. These samples will allow the investigators to analyze biomarkers-biological signals that can indicate increased or reduced cancer risk-before and after intervention.
Together, these approaches will provide information on whether metformin or naproxen are safe and well-tolerated in the FA population. As an additional outcome, by combining direct tissue analysis with biomarker studies, the investigators aim to detect subtle changes that precede cancer, giving us an early indication of whether the drugs are working as preventive agents.
Although this is an early-phase study, its potential significance is considerable. Demonstrating that well-tolerated, inexpensive, and widely accessible drugs may have potential to reduce cancer risk would represent a major advance for FA patients, who currently face limited options for prevention and treatment. This work may also offer insights relevant to broader cancer prevention efforts in other high-risk groups. Ultimately, our study seeks to take an important step toward changing the outlook for people with Fanconi anemia by moving the focus from late-stage treatment toward early prevention.
What's being tested
- Metformin
Intervention · DRUG
Oral metformin extended release, starting at a dose of 500mg daily and titrating up to 2000mg daily as tolerated for 6 months.
- Naproxen Sodium
Intervention · DRUG
6 months of oral naproxen sodium 440mg daily.
Study details
- Official title
- A Randomized Crossover Open-Label Trial of Naproxen and Metformin Safety and Tolerability in the Setting of Prevention of Oral Cancer in Fanconi Anemia
- Sponsor
- Rockefeller University
- Conditions
- Fanconi Anemia · Head and Neck Cancer · Squamous Cell Carcinoma · Squamous Cell Cancer of Head and Neck (SCCHN)
- Enrolling
- 80 people
- Starts
- 2026-10-14
- Est. completion
- 2031-10-14
- Design
- Open-label, randomized, crossover, Phase 1
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years and overSex ALLHealthy volunteers Not acceptedYou may qualify if
- Confirmed Diagnosis:
- Fanconi anemia confirmed by review of past molecular testing (including chromosomal breakage testing results) Age
- Age ≥18 years. Functional Status
- Karnofsky performance scale ≥70%. Adequate Organ and Marrow Function, defined as:; Leukocytes ≥3,000/µL; Absolute neutrophil count ≥1,000/µL; Platelets ≥40,000/µL; Total bilirubin ≤1.5 × institutional upper limit of normal (ULN) unless with Gilberts syndrome; AST (SGOT) / ALT (SGPT) ≤3 × institutional ULN; eGFR >45 mL/min (using CKD-EPI equation: https://www.mdcalc.com/ckd-epi-equations-glomerular-filtration-rate-gfr) Viral Infection Status; HIV-infected patients are eligible if on effective antiretroviral therapy with undetectable viral load within 6 months.; Chronic HBV infection is permitted if viral load is undetectable on suppressive therapy.; History of HCV infection is allowed if patient has been treated and cured, or if currently being treated and has undetectable viral load.; Patients on chronic suppressive antiviral therapy for HSV are eligible. Medication and Intervention Requirements; Ability to take oral medication. Contraception Agreement; Willing to use adequate contraception during the study, including: Barrier method, abstinence, vasectomized partner, effective birth control, or postmenopausal status.; Women of childbearing potential and men must agree to use contraception prior to study entry and throughout participation.; Female participants who become pregnant or suspect pregnancy must inform the study physician immediately. Consent - Ability to understand and willingness to sign a written informed consent form in English or an approved translated version. Alcohol, tobacco, and marijuana abstinence; Standard of care for oral leukoplakia is to recommend abstinence from smoking and alcohol consumption. As part of the consent, we will ask participants to agree to abstain from alcohol, tobacco, and marijuana.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
Loading treatment details…
Study locations (2)
2 openUniversity of MInnesota
Minneapolis, Minnesota, United States
- Rachel Uppgaard, DDS · Contact612-625-6976uppg0003@umn.edu
- Carla Campbell · Contact612-625-6976camp2757@umn.edu
RecruitingThe Rockefeller University
New York, New York, United States
- Francis J May, MD · Contact212-327-7850
- Yu-Chien Lin · Contact212-327-7850ylin@rockefeller.edu
Recruiting
Study team
Sponsor
Rockefeller University
Study ID FMA-1073
Principal investigator
Agata Smogorzewska, MD, PhD
The Rockefeller University
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.