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SAB Biotherapeutics, Inc. (SABS)·Q3 2021 Earnings Summary

Executive Summary

  • Advanced SAB-185 to Phase 3 in NIH-sponsored ACTIV-2 after a positive DSMB recommendation; first Phase 3 patient dosed in October, positioning near-term clinical catalysts in COVID-19 therapeutics .
  • Secured an additional $60.5M DoD award (cumulative ~$203M across four awards since March 2020), materially strengthening funding visibility for SAB-185 through licensure and commercial manufacturing .
  • Cash was $10.8M at September 30, 2021; pro forma cash was ~$30M post-October business combination—adequate to advance near-term trials but with rising OpEx from pipeline execution .
  • No quarterly revenue or EPS were disclosed and no earnings call transcript was available; comparisons to Street estimates are not possible given data constraints and the company’s newly public status .

What Went Well and What Went Wrong

What Went Well

  • Phase 3 advancement of SAB-185 in ACTIV-2 following DSMB review, with first Phase 3 patient dosed in October—demonstrates clinical momentum and external validation via NIH collaboration .
  • Incremental $60.5M DoD funding for SAB-185, bringing total announced awards to ~$203M since March 2020—de-risks late-stage development and manufacturing scale-up .
  • Management strengthened finance leadership, appointing CFO Russell Beyer (30+ years experience), supporting public-company readiness and execution .
  • Quote: “Our pipeline…continues to advance, and our clinical programs for SAB-185 and SAB-176 show strong therapeutic potential…” —Eddie J. Sullivan, PhD, President & CEO .

What Went Wrong

  • Nine months 2021 net loss of $5.6M versus net income of $11.7M in the prior-year period, reflecting intensified R&D and corporate build-out as programs advance .
  • R&D expenses rose sharply to $46.5M (9M21) from $12.6M (9M20), driven by SAB-185 advancement; while aligned with pipeline progress, it elevates near-term burn .
  • Item 4.02 restatement: reclassification of SPAC-related redeemable common stock and EPS methodology under ASC 480 and related guidance—no change to total assets/liabilities, but highlights internal control remediation needs .

Financial Results

Availability Note

The company did not disclose Q3 2021 quarterly revenue, EPS, or margin figures in its 8-K/press release, and no earnings call transcript was found. As a newly public company (October 2021 SPAC close), SABS provided nine-month year-to-date metrics rather than quarter-specific financials .

Cash and Operating Expenses (Nine Months to Date)

Metric9M 20209M 2021
Cash and Cash Equivalents (period-end)$13.5M $10.8M
R&D Expenses$12.6M $46.5M
G&A Expenses$4.9M $9.3M
Net Income (Loss)$11.7M $(5.6)M

Additional liquidity: Pro forma cash ~$30M post-Oct 22, 2021 business combination closing .

Revenue, EPS, Margins vs Prior Periods and Estimates

MetricQ2 2021Q3 2021Vs Prior QuarterVs Prior YearVs Estimates
Revenue ($USD)Not disclosed Not disclosed N/A N/A N/A (Unavailable)
Diluted EPS ($USD)Not disclosed Not disclosed N/A N/A N/A (Unavailable)
Gross/EBIT/Net Margins (%)Not disclosed Not disclosed N/A N/A N/A (Unavailable)

KPIs and Funding

KPICurrentPriorNotes
DoD Funding—Incremental Award$60.5M N/AExpanded scope for advanced clinical development to licensure
DoD Funding—Cumulative~$203M N/AFour awards since March 2020
SAB-185 Program StatusPhase 3 ACTIV-2 (NIH) Phase 2 DSMB recommended advancement; first patient dosed Oct 2021
SAB-176 Program StatusOngoing Phase 2a challenge study N/ATopline data expected Q4 2021

Guidance Changes

MetricPeriodPrevious GuidanceCurrent GuidanceChange
SAB-176 Topline Data TimingQ4 2021Not previously specifiedTopline Phase 2a expected Q4 2021 New timing detail
SAB-142 IND-Enabling StartQ1 2022Not previously specifiedIND-enabling studies expected to begin Q1 2022 New timing detail
Revenue, Margins, OpEx, OI&E, TaxFY/Q3 2021Not providedNot provided Maintained (no financial guidance provided)
DividendsFY/Q3 2021Not applicableNot applicable No change

Earnings Call Themes & Trends

No earnings call transcript was found for Q3 2021, limiting thematic comparison.

TopicPrevious Mentions (Q1 2021, Q2 2021)Current Period (Q3 2021)Trend
Business Combination/SPACQ1: SPAC operations; Q2: Business Combination Agreement signed; expected close in Q4 2021 Closed in Oct 2021; trades as SABS Completed/Transitioned to public biotech
R&D ExecutionSPAC had no operating revenues; focus on merger process SAB-185 advanced to Phase 3; SAB-176 Phase 2a ongoing Acceleration in clinical activities
FundingSPAC trust and warrants; no operating funding DoD +$60.5M; ~$203M cumulative awards Strengthened external funding
Regulatory/AccountingSPAC warrant classification restatements; controls remediation Item 4.02 restatement carried through merger process Continued remediation focus
Macro (COVID-19)COVID risk disclosures in SPAC context COVID-19 therapy focus (SAB-185) Direct program exposure to pandemic dynamics

Management Commentary

  • Prepared remarks emphasize platform strength and pipeline breadth: “Our pipeline of potent and scalable human polyclonal antibodies…continues to advance, and our clinical programs for SAB-185 and SAB-176 show strong therapeutic potential…” —Eddie J. Sullivan, PhD, President & CEO .
  • Strategic positioning post-public listing: “We entered the next stage of our growth with our recent debut as a public company…” —Eddie J. Sullivan .
  • Operating leadership: Appointment of CFO Russell Beyer to support scaling and financial rigor .

Q&A Highlights

  • No Q3 2021 earnings call transcript was found; therefore, no Q&A highlights or clarifications are available .

Estimates Context

  • Wall Street consensus (S&P Global) for Q3 2021 revenue and EPS was unavailable due to data access limitations and the company’s newly public status; as such, estimate comparisons cannot be made at this time .

Key Takeaways for Investors

  • Near-term clinical catalysts: Phase 3 ACTIV-2 progress for SAB-185 and Q4 2021 SAB-176 topline readout can be stock-moving events; monitor NIH ACTIV-2 updates and influenza challenge data releases .
  • Funding de-risking: The additional $60.5M DoD award (cumulative ~$203M) materially supports late-stage development and manufacturing planning for SAB-185, reducing near-term financing risk .
  • Operating ramp: Elevated R&D spend reflects advancing programs; pro forma cash (~$30M) plus awards underpin runway but remain sensitive to timeline and trial costs .
  • Accounting/controls: Restatement under Item 4.02 highlights ongoing internal control remediation; investors should watch audit progress and financial reporting cadence .
  • Data visibility: Lack of disclosed quarterly revenue/EPS and absence of a call transcript constrain near-term financial modeling; focus should be on clinical milestones and external funding milestones .
  • Strategic narrative: Polyclonal antibody platform positioned for variant-resilient responses in infectious diseases; success in Phase 3 and SAB-176 could broaden platform credibility and partnerships .

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