Immix Biopharma Inc
announced early interim data from IMMINENT-01 Phase 1b/2a trial combining tissue-specific therapeutic IMX-110 with BeiGene Ltd / Novartis AG's tislelizumab, for advanced solid tumors.100% Tumor Shrinkage at two months was observed in advanced metastatic colorectal cancer demonstrated by IMX-110 + tislelizumab combination in the first cohort of patients who received the lowest IMX-110 dose.
Tumor shrinkage was observed in the first two out of two (2/2) evaluable patients (100%) at two months.
The company compares the data with Merck & Co Inc's
anti-PD-1 antibody Keytruda (pembrolizumab) alone produced tumor shrinkage in 3 of 19 patients (16%) with an evaluable postbaseline tumor assessment in Phase 1b study of pembrolizumab in patients with advanced or metastatic colorectal cancer according to O'Neil et al., 2017.No dose-limiting toxicities have been observed in the first cohort. Hence the trial can now enroll the next cohort of three patients at a higher dose of IMX-110 + tislelizumab.
Immix Biopharma is enrolling the next higher dose cohort of IMX-110 + anti-PD-1 antibody tislelizumab in advanced solid tumors.
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