Using MASL to Combat Oral Cancer (NCT04188665) | Clinical Trial Compass
CompletedEarly Phase 1
Using MASL to Combat Oral Cancer
United States18 participantsStarted 2021-01-29
Plain-language summary
This project will evaluate the expression of a receptor called podoplanin (PDPN) in cells from oral cancers and precancerous lesions. We will also determine how sensitive oral cancer cells are to a potential drug called Maackia amurensis seed lectin (MASL).
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
✓. Males and females of at least 18 years of age who are able to give consent.
✓. Smokers and non-smokers.
✓. Persons with white or red spots and/or lesions suspected or found to be oral cancer or precancer on the inner surface of the mouth.
✓. Oral lesions will be classified as OSCC or leukoplakia including, proliferative verrucous leukoplakia, conventional erythroplakia, suspect oral papillomas, or oral lichen planus. Only patients with such histologically confirmed diagnoses will be considered for inclusion.
✓. patients will be considered for inclusion at any stage of disease progression.
✓. Patients will be considered for inclusion if a subsequent biopsy or surgical resection are planned as part of their best care treatment.
✓. Patients will have an Eastern Cooperative Oncology Group performance status of 0 or 1.
✓. Patients will display normal organ function as evidenced by standard laboratory blood tests including liver enzymes and creatine.
Exclusion criteria
✕. Patients with cognitive impairments and cannot consent for themselves.
✕. Patients with language/hearing impairments.
✕. Use of a topical steroid product within the last 2 weeks.
✕. Pregnant women (to avoid any potential risk to the fetus) to be confirmed by standard blood or urine tests according to best care practice.