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

Who is this study for? Adult patients with Head and Neck Squamous Cell Carcinoma
What treatments are being studied? Maackia amurensis Seed Lectin
Status: Active_not_recruiting
Location: See all (4) locations...
Intervention Type: Drug, Other
Study Type: Interventional
Study Phase: Early Phase 1
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).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
United States
New Jersey
New Jersey Medical School
Newark
Rutgers School for Dental Medicine
Newark
University Hospital
Newark
Rowan University
Stratford
Time Frame
Start Date: 2021-01-29
Completion Date: 2025-12-31
Participants
Target number of participants: 20
Treatments
Experimental: MASL treated
Patients treated with lozenge containing MASL
Placebo_comparator: Placebo treated
Patients treated with lozenge without MASL
Sponsors
Leads: Rowan University
Collaborators: Rutgers University

This content was sourced from clinicaltrials.gov