A Phase I/II Study of TheraT® Vector(s) Expressing Human Papillomavirus 16 Positive (HPV 16+) Specific Antigens in Patients with HPV 16+ Confirmed Cancers

Protocol No

HOOKIPA-H-200-001

Principal Investigator

Stuart Wong

Phase

I/II

Summary

In this study, different regimens of the study drug are planned to be explored to see which regimen is safe and works the best: -HB-201 alone -A regimen of HB-201 alternating with HB-202 -HB-201 in combination with an FDA-approved drug, Nivolumab -A regimen of HB-201 alternating with HB-202, in combination with an FDA-approved drug Nivolumab

Description

This study is to investigate the study drug in patients with a specific type of cancer called human papillomavirus 16-positive (HPV 16+) cancers. HPV 16+ cancers include head and neck, cervical, anal, vaginal, vulvar, and penile cancers. The main goal of the study is to determine whether HB-201 and HB-202 are effective in the treatment of human papillomavirus 16 positive (HPV 16+) confirmed cancers.

Participating Institutions

Froedtert Hospital

Status

OPEN TO ACCRUAL

Sub Category

Gynecologic Cancers, Early Phase/Multiple Disease Site Cancers, Head and Neck Cancers

ClinicalTrials.gov

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