CRX100, currently in Phase1b, represents the potential to engineer an immune response in the solid tumor microenvironment 1) at the level of activation of the innate immune system, previously undruggable, and 2) with subsequent immune targeting of specific disease processes in a full adaptive immune response. Thus, overcoming resistance and reducing cancer recurrence. The safe and dependable activation of the innate immune response has been illusive until now. BioEclipse’s Immunotherapeutics precisely initiate the appropriate innate immune response to modulate cells of the adaptive immune system. These cells can then recognize a variety of tumor cell molecules and attack those tumor cells. The patient’s endogenous antitumor immune cells are required for the long-term durability of the adaptive immune antitumor response.
Our low-cost allogeneic CRX200 offers superior advantages including 1) saving patients the burden of apheresis that all other cell therapies require at each infusion, 2) delivers more potent tumor killing per infusion thus reducing the number of infusions, and 3) lowers the dose of cells and payload.
Our allogeneic CRX200 have been de-risked by achieving in autologous phase 1 clinical trial through regulatory, manufacturing and cold chain shipping milestones.
IND Ready Proprietary Platform Targeting Solid Tumors CRX200
Link to clinicaltrials.gov
In general there are multiple challenges for refractory and resistant solid Malignancies. Challenges for Ovarian cancer specifically are that Patients are often first identified at an advanced stage of disease with 85% that become resistant to Standard of Care (SOC), 15% enter treatment already resistant to platinum drugs. Immunotherapies including CRX200 are promising as more effective treatments, especially if moved to first line or second line treatment.