SAB Biotherapeutics to Showcase SAB-142 Data at Key Diabetes and Immunology Conferences

  • SAB Biotherapeutics will present data on SAB-142 at ADA’s 2026 Scientific Sessions and FOCIS 2026 Annual Meeting in June.
  • Oral presentation at ADA on June 5, 2026, focusing on safety, pharmacokinetics, and immunogenicity of SAB-142.
  • Poster presentation at FOCIS on June 10, 2026, highlighting clinical translation of SAB-142 from juvenile NHP studies to humans.
  • SAB-142 is a disease-modifying, redosable immunotherapy for newly diagnosed Stage 3 type 1 diabetes (T1D).
  • Topline data readout for the Phase 2b SAFEGUARD study expected in the second half of 2027.

SAB Biotherapeutics’ presentations at ADA and FOCIS underscore the growing interest in disease-modifying immunotherapies for type 1 diabetes. The focus on SAB-142’s clinical and mechanistic profile highlights the company’s strategic push to establish its lead candidate as a potential best-in-class treatment. The upcoming topline data readout from the Phase 2b SAFEGUARD study will be critical in determining the therapeutic and commercial viability of SAB-142 in the competitive autoimmune disease market.

Clinical Efficacy
How the data from SAB-142’s Phase 2b SAFEGUARD study will impact its potential as a best-in-class therapy for T1D.
Regulatory Pathway
Whether the positive clinical translation data will accelerate regulatory approval timelines.
Market Positioning
The pace at which SAB Biotherapeutics can differentiate SAB-142 from existing treatments like rabbit ATG.