The PolarTrak is designed to precisely force the bacteria loaded with the drug to distribute in 3D throughout the volume of the tumor without circulating in the bloodstream, offering 3,500 times more drug inside the tumor than traditional chemotherapy. The PolarTrak creates a “magnetic sphere” around the tumor to contain them inside the tumor. This prevents the drug from circulating in the rest of the patient’s body, thereby preventing side effects.
Preclinical studies demonstrated that the Starpax Bn1-S™ bacteria fill the whole volume of the tumor, while accumulating in the hypoxic regions, and attack cancer cells, including the ones in the “low oxygen” hypoxic zones.
“Hypoxia causes slow-proliferating stem-cell-like phenotype of cells, decreases senescence, creates chaotic and malfunctioning blood vessels, which further induces therapy resistance.”
(The role of hypoxia in cancer progression. Barbara Muzz, Pilar de la Puente, Feda Azab, Abdell Kareem Azab, 2015)
The lack of blood vessels or their malfunction in the tumor greatly limits drug diffusion. The Bn1-S swim toward hypoxic zones where the oxygen level is the same as their culture medium. They circumvent obstacles, penetrate into hypoxic areas and distribute their drug effectively to the cancer stem-like cells.
Third-party preclinical studies of human cancer tumors grown in mice have shown that the Starpax Bn1-S™ accumulate the hypoxic region and that the treatment triggers the immune system with “deep infiltration” of the white blood cells (T-cells, NK cells, and macrophages) in the tumor. Studies have also shown that Bn1-S injected into the tumors alone without drugs generate significant tumor regression acting as an immunostimulant. Based on literature and preclinical results, it is expected that the Starpax treatment will cause a systemic immune response to attack floating cancer cells and remote metastases, without any drug circulating in the rest of the body.