SAB Biotherapeutics to Showcase SAB-142 Data at EASD 2026

  • SAB Biotherapeutics will present Phase 1 data on SAB-142 at the 62nd EASD Annual Meeting in Milan, September 28 - October 2, 2026.
  • Presentations will highlight SAB-142's mechanism of action, redosing safety, and early C-peptide preservation evidence in T1D patients.
  • SAB-142 is currently in a registrational Phase 2b trial (SAFEGUARD) for newly diagnosed Stage 3 T1D patients.
  • The company's proprietary technology uses transchromosomic cattle to produce fully human immunoglobulins.

SAB Biotherapeutics' presentation at EASD 2026 comes as the diabetes research community increasingly focuses on disease-modifying therapies that preserve insulin production. The company's proprietary platform for producing fully human immunoglobulins represents a potential breakthrough in treating autoimmune diseases, though it faces competition from established treatments like rabbit ATG. The success of SAB-142 could validate this novel approach and open new avenues for autoimmune disease treatment.

Clinical Efficacy
How SAB-142's early C-peptide preservation data will position it against existing T1D treatments.
Regulatory Pathway
The pace at which SAFEGUARD trial results could accelerate SAB-142's regulatory approval process.
Market Differentiation
Whether SAB-142's fully human immunoglobulin approach will provide a competitive advantage in the autoimmune disease space.