STOCK TITAN

SAB BIO to Present Additional Data Supporting the Unique Profile of SAB-142 at the 2026 Immunology of Diabetes Society Congress

Rhea-AI Impact
(Neutral)
Rhea-AI Sentiment
(Neutral)
Tags

SAB BIO (Nasdaq: SABS) will present additional clinical and mechanistic data for lead program SAB-142 at the 21st Immunology of Diabetes Society Congress, April 20-24, 2026, in Brisbane. Presentations include an oral symposium and multiple posters highlighting multi-specific binding and C-peptide findings. The SAFEGUARD study is actively enrolling with an anticipated topline readout in 2H 2027.

Presentation materials will be posted on the company website at the time of the conference.

Loading...
Loading translation...

Positive

  • None.

Negative

  • None.

News Market Reaction – SABS

+4.92%
1 alert
+4.92% News Effect

On the day this news was published, SABS gained 4.92%, reflecting a moderate positive market reaction.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

IDS Congress: 21st meeting Congress dates: April 20–24, 2026 Topline data timing: 2H 2027 +5 more
8 metrics
IDS Congress 21st meeting Immunology of Diabetes Society Congress where SAB-142 data will be presented
Congress dates April 20–24, 2026 Timing of IDS Congress in Brisbane for SAB-142 presentations
Topline data timing 2H 2027 Anticipated topline readout for Phase 2b SAFEGUARD study
Disease stage Stage 3 T1D Target population for SAB-142 in newly diagnosed type 1 diabetes
Oral presentation time Apr 22, 2026 | 1:00–1:45PM AEST Main SAB-142 oral presentation slot at IDS Congress
Poster session 1 Apr 21, 2026 | 5:30–7:00PM AEST Timing for two SAB-142-related posters in Poster Session 1
Poster identifiers #207, #264, #364 Poster numbers for SAB-142 mechanistic and assay presentations
Pre-news share price $3.86 Last close before IDS presentation announcement

Market Reality Check

Price: $3.85 Vol: Volume 620,431 is slightl...
normal vol
$3.85 Last Close
Volume Volume 620,431 is slightly below the 20-day average of 671,956 (relative volume 0.92). normal
Technical Trading above the 200-day MA at 3.18, with shares at 3.86 pre-announcement.

Peers on Argus

SABS is down about 1.03% while momentum-screened biotech peers like AKTX and XCU...
2 Up

SABS is down about 1.03% while momentum-screened biotech peers like AKTX and XCUR are up 7.56% and 8.43%, suggesting stock-specific trading rather than a broad sector move.

Historical Context

5 past events · Latest: Mar 19 (Negative)
Pattern 5 events
Date Event Sentiment Move Catalyst
Mar 19 Offering closing Negative -0.8% Closed $85M equity and warrant offering, adding dilution overhang.
Mar 17 Offering pricing Negative -9.1% Priced $85M equity and pre-funded warrant raise for SAB-142 program.
Mar 17 Offering proposed Negative -9.1% Announced plan for underwritten offering and potential 15% overallotment.
Mar 10 Clinical data update Positive +6.8% Additional Phase 1 SAB-142 data showing C-peptide preservation signals.
Mar 09 Earnings and pipeline Positive +6.8% Full-year 2025 results with cash runway through 2028 and SAB-142 progress.
Pattern Detected

Recent news flow shows consistent alignment between headline tone and price reaction: clinical and business updates saw gains, while financing announcements coincided with declines.

Recent Company History

Over the last month, SAB BIO issued several key updates. Financing steps in mid‑March 2026, including proposed, priced, and closed offerings around $85 million, all tagged as offerings, saw negative price reactions. In contrast, additional Phase 1 data for SAB‑142 on Mar 10 and full‑year 2025 results on Mar 9 each coincided with 6.77% gains. Today’s IDS presentation plan extends this ongoing focus on SAB‑142’s clinical profile and progression toward Phase 2b SAFEGUARD data in 2H 2027.

Market Pulse Summary

This announcement outlines upcoming oral and poster presentations for SAB‑142 at the IDS Congress, r...
Analysis

This announcement outlines upcoming oral and poster presentations for SAB‑142 at the IDS Congress, reinforcing its positioning in newly diagnosed Stage 3 T1D and the ongoing Phase 2b SAFEGUARD program, with topline data targeted in 2H 2027. In recent months, shareholders have seen a mix of supportive clinical signals and sizeable fundraising around $85 million. Key factors to watch include additional C‑peptide data, mechanistic insights, enrollment progress, and any updates to cash runway or development plans.

Key Terms

anti-thymocyte immunoglobulin, type 1 diabetes, immunotherapy, c-peptide, +4 more
8 terms
anti-thymocyte immunoglobulin medical
"developing a fully human anti-thymocyte immunoglobulin (hATG) for type 1 diabetes"
A preparation of antibodies, typically derived from animals, that selectively targets and reduces certain white blood cells to dampen the immune response. Investors should care because it is used to prevent organ transplant rejection and treat some immune disorders, so its safety, regulatory approvals, manufacturing capacity, and pricing affect drug developers, hospital demand, and revenue prospects in immunology and transplant markets — like a dimmer switch controlling the body’s immune alarm.
type 1 diabetes medical
"for type 1 diabetes (T1D) and other autoimmune diseases"
An autoimmune condition in which the pancreas stops producing insulin, a hormone that lets the body use sugar for energy; without insulin people must manage blood sugar with injections, pumps, or other therapies. For investors, it matters because the lifelong need for medicines, devices, and monitoring creates steady demand, influences healthcare spending and reimbursement decisions, and drives clinical trials and regulatory activity in the diabetes treatment market.
immunotherapy medical
"a potentially best-in-class, disease-modifying, redosable immunotherapy in clinical development"
Treatment that uses or enhances the body’s immune system to detect and fight disease, most often cancers or chronic infections; think of it as training or arming the body’s own soldiers to find and destroy targets. It matters to investors because successful immunotherapies can lead to high-value drug approvals, recurring revenue from long-term treatments, and changes in competitive dynamics, while failures or safety issues in clinical trials can materially affect company valuations.
c-peptide medical
"additional C-peptide data from our patient cohort, which we believe underpins"
C‑peptide is a short protein fragment released at the same time the pancreas produces insulin; because it lingers in the blood longer than insulin itself, clinicians measure C‑peptide levels as a clear sign of how much natural insulin a person still makes. For investors, C‑peptide matters because it’s used as a measurable outcome in diabetes drug and device trials, in diagnostic tests, and by regulators to judge treatment benefit — results that can affect clinical success, approvals, and market value.
pbmc medical
"a PBMC based flow cytometry pharmacokinetic assay linking target engagement"
PBMC stands for peripheral blood mononuclear cells, a mixed group of immune cells such as lymphocytes and monocytes isolated from a blood sample. Investors should care because PBMCs are commonly used in research and clinical testing to measure immune responses, screen drug effects, and develop cell therapies; results that rely on PBMCs can affect a drug’s development timeline, regulatory review and commercial prospects, much like a test crew that vets a product before rollout.
flow cytometry medical
"a PBMC based flow cytometry pharmacokinetic assay linking target engagement"
A laboratory method that uses lasers and sensors to count and analyze individual cells or tiny particles as they flow past a detector, like a high‑speed supermarket scanner that reads barcodes on each item. Investors care because flow cytometry is widely used in drug development, diagnostics and manufacturing quality control; demand for the instruments, reagents and services can signal progress in clinical programs, recurring revenue streams and adoption of new therapies or tests.
pharmacokinetic medical
"flow cytometry pharmacokinetic assay linking target engagement to clinical exposure"
Pharmacokinetic describes how a drug moves through and leaves the body — how it is absorbed, spread to tissues, broken down and excreted — like tracking a package from pickup to delivery and disposal. For investors, these properties determine effective dose, safety risks, how often a medicine must be taken, and how reliably it works, which in turn influence clinical trial success, regulatory approval chances, production complexity and a drug’s commercial value.
autoimmune medical
"for type 1 diabetes (T1D) and other autoimmune diseases, today announced"
An autoimmune condition is when the body’s natural defense system mistakenly attacks healthy tissues, like a security guard that can’t tell residents from intruders. For investors, autoimmune diseases matter because they create long-term treatment needs, ongoing healthcare costs, and large markets for drugs, diagnostics, and devices; progress or setbacks in therapies, clinical trials, or approvals can strongly affect the value of companies working in this area.

AI-generated analysis. Not financial advice.

MIAMI, April 15, 2026 (GLOBE NEWSWIRE) -- SAB Biotherapeutics, Inc. (Nasdaq: SABS), a clinical-stage biopharmaceutical company developing a fully human anti-thymocyte immunoglobulin (hATG) for type 1 diabetes (T1D) and other autoimmune diseases, today announced that the Company will give an oral presentation and multiple poster presentations at the 21st Immunology of Diabetes Society (IDS) Congress being held April 20-24, 2026, in Brisbane, Australia. Data to be presented will highlight SAB BIO’s lead program, SAB-142, a potentially best-in-class, disease-modifying, redosable immunotherapy in clinical development for newly diagnosed Stage 3 T1D patients.

Alexandra Kropotova, M.D., MBA, Chief Medical Officer, SAB BIO, stated, “IDS is an important forum for us to present the breadth of SAB-142's clinical and mechanistic profile. We are pleased to share data on SAB-142's multi-specific binding profile and additional C-peptide data from our patient cohort, which we believe underpins its best-in-class potential. With the SAFEGUARD study now actively enrolling, we look forward to continued engagement with the T1D scientific community as we advance toward our anticipated topline data readout for this study in the 2H 2027.”  

Oral Presentation:

TitleSave All Beta Cells: Sustained Autoimmune Balance with SAB-142 Induction and Maintenance Dosing
Session: SAB BIO Industry Symposium
Presenters: John Wentworth, PhD, FRACP, Professor of Medicine*, Alexandra Kropotova, MD, MBA, Chief Medical Officer, SAB BIO; Christoph Bausch, PhD, MBA, Chief Operating Officer, SAB BIO
Presentation Date and Time: Wednesday, April 22, 2026 | 1:00 – 1:45PM AEST
Location:   Boulevard Auditorium
*Dr. Wentworth is an independent guest speaker and is not affiliated with SAB BIO.

Oral Poster Presentations:

TitleMulti-specific binding profile of SAB-142, a fully human anti-thymocyte globulin, against T-cell surface proteins
Session: Poster Session 1 – Poster #207
Presenter: Christoph Bausch, PhD, MBA, Chief Operating Officer, SAB BIO
Presentation Date and Time: Tuesday, April 21, 2026 | 5:30 – 7:00PM AEST
Location:  Boulevard Foyer

TitleTracking multiplicity for SAB142: a PBMC based flow cytometry pharmacokinetic assay linking target engagement to clinical exposure
Session:  Poster Session 1 – Poster #264
Presenter: Eric Sandhurst, PhD, Director, Program Management, SAB BIO
Presentation Date and Time: Tuesday, April 21, 2026 | 5:30 – 7:00PM AEST
Location:  Boulevard Foyer

TitleThe challenge of blood preservation from multicenter clinical trials: assessing whole blood preservation methods for analysis by flow cytometry
Session: Poster Session 2 – Poster #364
Presenter: Eric Sandhurst, PhD, Director, Program Management, SAB BIO
Presentation Date and Time: Wednesday, April 22, 2026 | 5:30 – 7:00PM AEST
Location:  Boulevard Foyer

The presentations will be made available in the Presentations section of the Company’s website at the time of the presentation and will remain accessible following the conference.

About SAB-142
SAB-142 is a potentially disease-modifying, redosable immunotherapy in clinical development for the treatment of autoimmune type 1 diabetes (T1D). SAB-142 is a multi-specific, fully human anti-thymocyte globulin (hATG) with a mechanism of action analogous to that of rabbit ATG (rATG). rATG has demonstrated in multiple clinical trials the ability to slow disease progression in patients with new- or recent-onset of Stage 3 T1D. SAB-142, like rATG, directly targets multiple immune cells involved in destroying pancreatic beta cells, including modulation of “bad acting” T-lymphocytes. By stopping immune cells from attacking beta cells, this treatment has the potential to preserve insulin-producing beta cells.

About SAB BIO
SAB BIO is a clinical-stage biopharmaceutical company focused on developing multi-specific, high-potency, human immunoglobulin G (hIgG) to treat and prevent immune and autoimmune disorders. Using advanced genetic engineering and antibody science, SAB BIO developed a proprietary technology which holds the potential to generate additional novel therapeutic candidates utilizing the human immune response, without the need for human donors or convalescent plasma. SAB BIO has optimized genetic engineering in the development of transchromosomic cattle, or Tc-Bovine, to produce hIgG. SAB BIO’s drug development production system is able to generate a diverse repertoire of specifically targeted, high-potency, hIgGs that can address a wide range of serious unmet needs in human diseases. The Company’s lead candidate, SAB-142, targets autoimmune T1D with a disease-modifying therapeutic approach that aims to change the T1D treatment paradigm by delaying onset and potentially preventing disease progression of Stage 3 T1D patients. SAB-142 is currently being evaluated in newly diagnosed Stage 3 autoimmune T1D patients in a registrational Phase 2b clinical trial called SAFEGUARD. For more information, visit www.sab.bio.

Forward-Looking Statements
Certain statements made in this press release that are not historical facts are forward-looking statements for purposes of the safe harbor provisions under The Private Securities Litigation Reform Act of 1995. Forward-looking statements generally are accompanied by words such as “believe,” “may,” “will,” “to be,” “estimate,” “continue,” “anticipate,” “intend,” “expect,” “should,” “would,” “plan,” “predict,” “potential,” “seem,” “seek,” “future,” “outlook,” and similar expressions that predict or indicate future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited to, statements regarding future events, including statements about the development and clinical trial results of the Company’s T1D program and other discovery programs.

These statements are based on the current expectations of SAB BIO and are not predictions of actual performance, and are not intended to serve as, and must not be relied on, by any investor as a guarantee, prediction, definitive statement, or an assurance, of fact or probability. These statements are only current predictions or expectations, and are subject to known and unknown risks, uncertainties and other factors which may be beyond our control. Actual events and circumstances are difficult or impossible to predict, and these risks and uncertainties may cause our or our industry’s results, performance, or achievements to be materially different from those anticipated by these forward-looking statements. A further description of risks and uncertainties can be found in the sections captioned “Risk Factors” in our most recent annual report on Form 10-K, subsequent quarterly reports on Form 10-Q, as may be amended or supplemented from time to time, and other filings with or submissions to, the U.S. Securities and Exchange Commission, which are available at https://www.sec.gov/. Except as otherwise required by law, SAB BIO disclaims any intention or obligation to update or revise any forward-looking statements, which speak only as of the date they were made, whether as a result of new information, future events, or circumstances or otherwise.

CONTACTS

Investor Relations:
Christine Ryan
ir@sab.bio

Media:
Sheila Carlson
media@sab.bio


FAQ

What data will SAB BIO (SABS) present for SAB-142 at the IDS Congress April 20-24, 2026?

They will present clinical and mechanistic data including multi-specific binding and C-peptide results. According to the company, materials cover SAB-142’s binding profile, additional C-peptide data from their patient cohort, and flow cytometry assays linking target engagement to clinical exposure.

When and where is SAB BIO’s oral presentation on SAB-142 at the 2026 IDS Congress?

The oral presentation is April 22, 2026, 1:00–1:45 PM AEST in the Boulevard Auditorium. According to the company, it is part of the SAB BIO Industry Symposium featuring senior company presenters and an independent guest speaker, John Wentworth, PhD.

How can investors access SAB BIO (SABS) presentations from the 2026 IDS Congress?

Presentations will be posted in the Presentations section of the company website when delivered. According to the company, materials will be available at presentation time and remain accessible after the conference for investor and scientific review.

What is the enrollment status and expected timeline for SAB BIO’s SAFEGUARD study (SABS)?

The SAFEGUARD study is actively enrolling and the company anticipates topline data in 2H 2027. According to the company, ongoing enrollment supports their plan to report anticipated topline results in the second half of 2027.

Which SAB BIO (SABS) posters at IDS 2026 describe pharmacokinetic or assay methods for SAB-142?

Poster #264 links a PBMC-based flow cytometry PK assay to clinical exposure and target engagement. According to the company, this poster describes a pharmacokinetic assay tracking multiplicity for SAB-142 and its clinical relevance.

What clinical potential does SAB-142 have according to SAB BIO (SABS) presentations at IDS 2026?

SAB-142 is presented as a potentially best-in-class, redosable, disease-modifying immunotherapy for newly diagnosed Stage 3 T1D. According to the company, their data aim to underscore multi-specific binding and C-peptide preservation that support this potential.