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SAB Biotherapeutics (SABS) Q2 2026 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for SAB Biotherapeutics Inc

Q2 2026 earnings summary

6 Aug, 2026

Executive summary

  • SAB-142, a fully human anti-thymocyte immunoglobulin, is advancing in pivotal clinical trials for Type 1 diabetes, targeting a multibillion-dollar market opportunity and supported by promising Phase 1 data on C-peptide preservation and glycemic control.

  • Over 60 clinical sites are recruiting for the SAFEGUARD Phase II-B trial, with enrollment on track for completion in Q4 2026 and topline data expected in the second half of 2027.

  • PRISE-hATG Phase III study, co-funded with Breakthrough T1D, expands eligibility to patients up to two years from diagnosis and will enroll 108 participants across three cohorts.

  • Construction began on a second farm facility in South Dakota to expand manufacturing capacity, ensure long-term commercial supply, and reduce operational risk.

  • Inclusion in the Russell 3000® and Russell 2000® indexes in June 2026 increased visibility among institutional investors.

Financial highlights

  • Ended Q2 2026 with $208 million in cash, cash equivalents, and investment securities, providing operational runway through 2028.

  • R&D expenses rose to $16.2 million in Q2 2026 from $7 million in Q2 2025, driven by clinical trial costs and increased headcount.

  • G&A expenses increased to $7.2 million from $2.7 million year-over-year, mainly due to higher headcount and stock-based compensation.

  • Net loss for Q2 2026 was $22.5 million, up 122% year-over-year; six-month net loss was $41.4 million, up 170%.

  • Other income was $0.9 million in Q2 2026, compared to an expense of $0.4 million in Q2 2025, reflecting higher investment income.

Outlook and guidance

  • SAFEGUARD enrollment is on track for completion in Q4 2026, with top-line data expected in the second half of 2027.

  • PRISE-hATG study to begin enrolling in the second half of 2026, with top-line results anticipated in Q1 2029.

  • Operational runway is projected through 2028, supporting ongoing clinical trials and pre-commercial activities; additional capital may be required for long-term plans.

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