SAB BIO announces positive topline Phase 1 clinical results with potentially disease-modifying T1D therapy SAB-142

Biopharmaceutical News

SAB BIO announces positive topline Phase 1 clinical results with potentially disease-modifying T1D therapy SAB-142
DiabetesEndocrinologyImmunoglobulin
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SAB BIO, (“SAB BIO”), a clinical-stage biopharmaceutical company with a novel immunotherapy platform that is developing human anti-thymocyte immunoglobulin (hIgG) for delaying the onset or progression of type 1 diabetes (T1D), today announced positive topline data from a Phase 1 trial of SAB-142 in a single-ascending dose among healthy volunteers.

SAB BIOFeb 6 2025 SAB BIO, , a clinical-stage biopharmaceutical company with a novel immunotherapy platform that is developing human anti-thymocyte immunoglobulin for delaying the onset or progression of type 1 diabetes , today announced positive topline data from a Phase 1 trial of SAB-142 in a single-ascending dose among healthy volunteers. The study met its primary objectives related to safety and pharmacodynamic activity enabling SAB-142 to advance to Phase 2b clinical development.

Phase 1 trial summary data The SAB-142 Phase 1 trial was designed as a randomized, double-blind, placebo-controlled, single-ascending dose, adaptive design clinical study among healthy volunteers and one cohort of participants with T1D. The objectives include establishing the safety, tolerability, pharmacokinetic , immunogenicity and pharmacodynamic profile for SAB-142.

Based on the data, SAB BIO plans to advance SAB-142 into a Phase 2b trial in 2025 to evaluate the therapeutic candidate in adult and pediatric patients with new-onset T1D.

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