Fact CheckerSign in

NCT04188665CompletedEarly phase 1

Using MASL to Combat Oral Cancer

Using Maackia Amurensis Seed Lectin to Target the Podoplanin Receptor as a Functionally Relevant Biomarker to Inhibit the Growth of Oral Squamous Cell Carcinoma and Precancerous Lesions

Source: ClinicalTrials.gov · Last updated 20 Mar 2026

Brief summary (registry, in English)

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).

Status (registry)
Completed
Phase (registry)
Early phase 1
Study type
Interventional
Enrollment
18 (actual)
First submitted
19 Nov 2019
Start date
Jan 2021
Primary completion date
Dec 2024
Lead sponsor
Rowan University
NCT number
NCT04188665

What you commit to

  • Study type: Interventional · Early phase 1
  • Participants enrolled: 18
  • From Jan 2021 to the primary completion date, Dec 2024
  • 4 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of a topical steroid product within the last 2 weeks.

Other

  • Patients with cognitive impairments and cannot consent for themselves.
  • Patients with language/hearing impairments.
  • Pregnant women (to avoid any potential risk to the fetus) to be confirmed by standard blood or urine tests according to best care practice.
  • Patients who are breastfeeding.
  • Abstinence or use of adequate contraception will be required for women of childbearing potential and men of reproductive potential.

Who the study is looking for

  • 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.
  • Patients will not present evidence of comorbidities including ongoing or active infection, unstable illness, or medical conditions.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital
Coordinator of this site? Confirm its status
NewarkUnited StatesUnknown status
Rutgers School for Dental Medicine
Coordinator of this site? Confirm its status
NewarkUnited StatesUnknown status
New Jersey Medical School
Coordinator of this site? Confirm its status
NewarkUnited StatesUnknown status
Rowan University
Coordinator of this site? Confirm its status
StratfordUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.