- CRB-601 is a highly potent and selective anti -?v?8 integrin monoclonal antibody designed to block the activation of TGF b in the local tumor microenvironment
- Additional non-clinical data demonstrates combination benefit across a diverse range of syngeneic models with differential sensitivity to checkpoint inhibition
- Anti-tumor activity correlates with increases in proliferating CD4+ and CD8+ T-cells as well as the NK cell population and a shift towards M1 macrophage polarization, supporting the hypothesis the CRB-601 may overcome immune cell exclusion
NORWOOD, Mass. , May 11, 2022 /PRNewswire/ -- Corbus Pharmaceuticals Holdings, Inc. (NASDAQ: CRBP) ("Corbus" or the "Company"), an immunology company, announced that new preclinical data for CRB-601 are being presented today in an oral presentation at the New York Academy of Sciences (NYAS) Frontiers in Cancer Immunotherapy Conference in New York, NY .
The latest preclinical data for CRB-601 demonstrate its significant effects on inhibiting tumor growth as a single agent and in combination with anti-PD-1 treatment in the MC38 and EMT6 syngeneic tumor models. In addition, CRB-601 restores an anti-PD-1 effect in the 4T1 syngeneic tumor model, a "cold" immune cell-depleted tumor model, when added in combination. This data marks the first time such an effect has been documented in this model with an anti-?v?8 agent.
The anti-tumor effects in the immune excluded EMT6 model correlated with changes in the immune cell populations in the tumor micro-environment. There were increases in proliferating CD4+ and CD8+ T-cells, NK cells, and a shift in macrophage polarization to the inflammatory M1 phenotype. Collectively these data suggest that treatment with CRB-601 could overcome the immune excluded phenotype established in this model and enhance the efficacy of treatment with anti-PD-1 therapy.
Additionally, in a rechallenge model, tumor-bearing mice initially rendered tumor-free by treatment with CRB-601 + anti-PD-1 were subsequently reinoculated with the same tumor cells (MC38) and monitored for tumor regrowth. After 30 days no tumors had formed in this cohort of animals, whereas all the treatment naïve control mice succumbed to the burden of tumor growth. These data illustrate that the combination treatment of CRB-601 + anti-PD-1 led to durable T-cell memory protection.
"CRB-601 demonstrates robust pre-clinical anti-tumor activity alone and in combination with anti-PD-1 therapy in tumors exhibiting a range of immune involvement. The ability of CRB-601 to significantly reduce the growth of tumors that are non-responsive to checkpoint inhibition and to re-sensitize these tumors to checkpoint blockade continues to support our hypothesis that effective blockade of TGF? should lead to immune cell perfusion and manifest the benefit of anti-PD-1 therapy. The orchestration of a response involving both the adaptive and innate arms of the immune system by CRB-601 is especially compelling," commented Rachael Brake , Ph.D., Chief Scientific Officer of Corbus.
Corbus is currently developing CRB-601 as a potential treatment for solid tumor cancers, and the program is advancing toward an IND submission in the first half of 2023.
The NYAS presentation is available on the Company website at: corbuspharma.com/NYASpresentation
Corbus is an immunology company committed to connecting innovation to our purpose of improving lives by developing new medicines that target the nexus between the immune system and cancer. Corbus' current pipeline includes anti-integrin monoclonal antibodies that block activation of TGF? and small molecules that activate or inhibit the endocannabinoid system. Corbus is headquartered in Norwood, Massachusetts . For more information on Corbus, visit corbuspharma.com . Connect with us on Twitter , LinkedIn and Facebook .
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SOURCE Corbus Pharmaceuticals