In the virus-inducible diabetes model, early discontinuation of ACT-777991 on Day 28 after infection showed a trend in improving the remission rate compared to aCD3 monotherapy, but to a lesser extent as compared to the chronic setting, suggesting the benefit of continuous blockade of the CXCR3 axis to revert diabetes.
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Combination treatment of a novel CXCR3 antagonist ACT-777991 with an anti-CD3 antibody synergistically increases persistent remission in experimental models of type 1 diabetes.
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