Candida Therapeutic Vaccine in Head and Neck Cancer Patients to Reduce Recurrence

University of Arkansas

Status and phase: Enrolling; Phase 2

Conditions: Squamous Cell Carcinoma of Head and Neck

Treatments: Biological: 0.5 mL Candin®/injection; Other: Placebo: 0.5 mL Intravenous 0.9% NaCl solution (Saline)

Study type: Interventional

Funder types: Other

Identifiers

NCT05952934

275695

Details and patient eligibility

About

This is a Phase II randomized, double-blind, placebo controlled, multi-site study of Candin. It is designed to show the efficacy and safety of a 7-dose regimen of Candin over a two-year period in terms of reducing cancer recurrence rate by comparing the recurrence rates between the Candin and the placebo arm. The ratio of the number of subjects who will receive Candin versus placebo will be 3:1. Up to 100 subjects will be screened until 80 subjects are eligible for injection.

Full description

This is a Phase II study to evaluate the efficacy and safety of a therapeutic vaccine called Candin® (Nielsen Biosciences, San Diego, CA) in adults over a two (2) year period. Each subject will be receiving a total of 7 injections of Candin (0.5 mL per dose) or placebo (saline) at a 3:1 ratio in a randomized double-blinded design. Subjects will receive one injection every 3 weeks until they receive 4 injections. Then, subjects will receive one injection every 3 months until they receive a total of 7 injections. Subjects will have 2 more visits approximately 6 months apart after the last injection. Immunological assessment T-cell repertoire analysis and by fluorescent activated cell sorter analysis (FACS) will be made at 4 time points (Visits 1, 5, 7, and 8). Stool and oral wash samples will be collected at the Screening Visit, Visit 5, Visit 7 and Visit 8 for microbiome diversity analysis.

Enrollment: 100 estimated patients

Sex: All

Ages: 18 to 100 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Able to provide informed consent
• Male or female 18 years of age or older
• Squamous cell carcinoma of the head and neck who have completed curative therapy (surgery and/or radiation and/or chemotherapy) within the previous 120 days.
• No Evidence of Disease (NED) based on clinical and/or radiographic evaluations
• Willing and able to comply with the requirements of the protocol

Exclusion criteria

• Positive urine pregnancy test for women of childbearing potential
• Being pregnant or attempting to be pregnant with the period of study participation
• Women who are breast feeding or plan to breast feed within the period of study participation
• Patients who are allergic to Candin®
• If in the opinion of the PIs or other Investigators, it is not in the best interest of the patient to enter or continue in this study

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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100 participants in 2 patient groups, including a placebo group

Candin vaccine

Active Comparator group

Description:

Seven Candida (Candin). The route of administration is intradermal injection at subject's limbs at 0.5 mL/injection. The schedule is 1 injection every three weeks for the first 4 injections, and then one injection every 3 months until a total of 7 injections has been given.

Treatment:

Biological: 0.5 mL Candin®/injection

Placebo

Placebo Comparator group

Description:

Seven placebo injections (sterile 0.9% Normal Saline). The route of administration is intradermal injection at subject's limbs at 0.5 mL/injection. The schedule is 1 injection every three weeks for the first 4 injections, and then one injection every 3 months until a total of 7 injections has been given.

Treatment:

Other: Placebo: 0.5 mL Intravenous 0.9% NaCl solution (Saline)