Intensity Therapeutics reports that INT230-6’s Anti-cancer Mechanism is a Combination of Cell Death with Immune System Activation

Intensity Therapeutics, Inc., a privately held biotechnology company developing proprietary immune cell-activating cancer treatments, announced that Chief Medical Officer Dr. Ian B Walters will be presenting mechanism of action and other data in a poster session at the American Academy of Cancer Research (AACR) meeting on April 19, 2016. The research being presented indicates that INT230-6 induces significant cancer cell death in the tumor microenvironment. Thereafter, eradication of the tumor by INT230-6 requires T lymphocytes and leads to a potent and durable systemic anti-cancer T-cell-dependent immunity against the tumor.

A series of preclinical studies conducted by the Company in collaboration with scientists from the Vaccine Branch at the National Cancer Institute (NCI) showed that following one cycle of five daily injections of low-dose INT230-6 into large mouse Colon26 tumors, 75% of the cancer cells die by day 3. Within 10 days of injection there was an increased influx of dendritic cells into the tumors, which are cells that can activate T-cells. Up to 80% of mice treated with INT230-6 experienced a complete response (CR) and became fully protected from re-inoculation challenges of the colon cancer. Both the treatment effect leading to CRs and the subsequent protective effect against re-inoculation decreased when CD4- and CD8-positive T-cells were depleted prior to treatment or re-challenge respectively. Protection was eliminated completely when both CD4 and CD8 T-cells were simultaneously depleted. Together the data indicate that the observed complete response and durable, vaccine-like anti-cancer effect of INT230-6 is a result of the direct cytotoxic nature of the drug and the formation of CD4- and CD8-positive immunological cell memory.

Chief Executive Officer Lewis H. Bender explained, “We plan to initiate clinical studies of INT230-6 as soon as possible. If our preclinical results translate in cancer patients, INT230-6 could represent a significant advance in the treatment of many types of solid tumor cancers, potentially providing oncologists with a less toxic means to destroy visible tumors, eliminate metastases and prevent disease recurrence.”

Presentation Details
Poster Title: A novel immunotherapy, INT230-6, is able to induce high rates of complete and durable response in mice through a cytotoxic T-cell-dependent mechanism
Authors: Ian B. Walters MD and Lewis H. Bender of Intensity Therapeutics; Anja C. Bloom PhD, Masaki Terabe PhD, and Jay A. Berzofsky MD, PhD of the Vaccine Branch, Center for Cancer Research, NCI
Session Category: Immunology
Session Title: Immune Modulation from Non-Immunotherapy: Preclinical
Session Date and Time: Tuesday Apr 19, 2016 1:00 PM – 5:00 PM local time
Location: Ernest N. Morial Convention Center, New Orleans, LA, Halls G-J, Poster Section 26

About INT230-6
INT230-6 is a novel, anti-cancer drug product able to disperse through tumors and diffuse into cancer cells. The product was identified from Intensity’s DfuseRxSM platform technology. In in vivo preclinical models of severe cancer, INT230-6 treatment results in substantial improvement in overall survival compared to standard therapies. The product can completely clear large tumors in animal models. Complete responders have long-term protection even after multiple re-inoculations of the cancer. INT230-6 administration has shown an increased recruitment of immune cells to the tumor microenvironment. Intensity Therapeutics anticipates making an Investigational New Drug (IND) application to the U.S. FDA in 2016 to commence Phase 1 clinical studies.