SAB Biotherapeutics will present data on SAB-142, an immunotherapy for type 1 diabetes, at ATTD-Asia 2025 in Singapore.
Quiver AI Summary
SAB Biotherapeutics, Inc. announced that it will present data on its lead program, SAB-142, at the 2nd Asian Conference on Innovative Therapies for Diabetes Management (ATTD-Asia) in Singapore from December 9-11, 2025. SAB-142 is a human anti-thymocyte immunoglobulin (hATG) currently in clinical development aimed at treating type 1 diabetes (T1D) and other autoimmune diseases. The presentations will cover Phase 1 study findings, demonstrating SAB-142's mechanism of action, immunomodulation without significant side effects, and a favorable safety profile. The company's Chief Medical Officer expressed enthusiasm about sharing this data and the progress toward the Phase 2b clinical trial, which aims to delay T1D progression in newly diagnosed Stage 3 patients. For more information, details of the presentations will be available on the company's website after they occur.
Potential Positives
- SAB Biotherapeutics will present data on SAB-142 at a major international conference, which can enhance visibility and credibility in the biopharmaceutical community.
- The Phase 1 study data presented demonstrates a favorable safety profile for SAB-142, which may attract further investment and interest in its development.
- The focus on a potentially best-in-class, disease-modifying immunotherapy for delaying T1D progression positions SAB Biotherapeutics as a key player in an important therapeutic area with significant unmet need.
Potential Negatives
- Data presented at a conference may highlight the progress of the company's lead program, but it also places pressure on SAB Biotherapeutics to deliver positive results in ongoing clinical trials, raising concerns about its ability to meet expectations.
- The reliance on forwarding-looking statements without definitive outcomes may create skepticism among investors about the company's future performance and the actual potential of SAB-142.
- The company faces significant competition in the biopharmaceutical space, particularly regarding innovative therapies for managing diabetes, which may affect its market position and investor confidence.
FAQ
What is SAB Biotherapeutics' lead program?
SAB Biotherapeutics' lead program is SAB-142, a potentially best-in-class immunotherapy for type 1 diabetes.
When will SAB Biotherapeutics present at ATTD-Asia?
SAB Biotherapeutics will present at the 2nd Asian Conference on Innovative Therapies for Diabetes Management from December 9-11, 2025.
What are the key findings from the SAB-142 Phase 1 study?
The findings include a multi-specific mechanism of action, absence of sustained lymphodepletion, and a favorable safety profile.
Who is presenting the SAB-142 data?
The data will be presented by Christoph Bausch, PhD, and Stan Stoyanov, MD, at the conference.
How does SAB-142 work in treating type 1 diabetes?
SAB-142 targets multiple immune cells to stop the destruction of insulin-producing pancreatic beta cells.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$SABS Hedge Fund Activity
We have seen 22 institutional investors add shares of $SABS stock to their portfolio, and 9 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- VIVO CAPITAL, LLC added 11,420,000 shares (+inf%) to their portfolio in Q3 2025, for an estimated $22,954,199
- COMMODORE CAPITAL LP added 4,401,500 shares (+inf%) to their portfolio in Q3 2025, for an estimated $8,847,014
- RA CAPITAL MANAGEMENT, L.P. added 4,401,500 shares (+inf%) to their portfolio in Q3 2025, for an estimated $8,847,014
- WOODLINE PARTNERS LP added 2,850,881 shares (+inf%) to their portfolio in Q3 2025, for an estimated $5,730,270
- SESSA CAPITAL IM, L.P. added 1,740,000 shares (+379.5%) to their portfolio in Q3 2025, for an estimated $3,497,399
- SPHERA FUNDS MANAGEMENT LTD. added 566,395 shares (+inf%) to their portfolio in Q3 2025, for an estimated $1,138,453
- HB WEALTH MANAGEMENT, LLC added 307,500 shares (+inf%) to their portfolio in Q3 2025, for an estimated $618,074
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
$SABS Analyst Ratings
Wall Street analysts have issued reports on $SABS in the last several months. We have seen 2 firms issue buy ratings on the stock, and 0 firms issue sell ratings.
Here are some recent analyst ratings:
- Chardan Capital issued a "Buy" rating on 11/17/2025
- HC Wainwright & Co. issued a "Buy" rating on 07/22/2025
To track analyst ratings and price targets for $SABS, check out Quiver Quantitative's $SABS forecast page.
$SABS Price Targets
Multiple analysts have issued price targets for $SABS recently. We have seen 3 analysts offer price targets for $SABS in the last 6 months, with a median target of $9.0.
Here are some recent targets:
- Keay Nakae from Chardan Capital set a target price of $12.0 on 11/17/2025
- An analyst from Leerink Partners set a target price of $7.0 on 09/17/2025
- Emily Bodnar from HC Wainwright & Co. set a target price of $9.0 on 07/22/2025
Full Release
MIAMI, Dec. 08, 2025 (GLOBE NEWSWIRE) -- SAB Biotherapeutics, Inc. (Nasdaq: SABS ), a clinical-stage biopharmaceutical company developing human anti-thymocyte immunoglobulin (hATG) for type 1 diabetes (T1D) and other autoimmune diseases, today announced that the Company will give several oral presentations at the 2 nd Asian Conference on Innovative Therapies for Diabetes Management (ATTD-Asia) being held December 9-11, 2025, in Singapore.
Data to be presented will highlight the progress of SAB BIO’s lead program, SAB-142, a potentially best-in-class, disease-modifying, redosable immunotherapy in clinical development for delaying the progression of T1D in new-onset, Stage 3 patients, including:
- Phase 1 study data showcasing the clinically validated, multi-specific mechanism of action of SAB-142.
- Phase 1 study data demonstrating immunomodulation without sustained lymphodepletion following dosing of SAB-142.
-
Phase 1 study data demonstrating a favorable safety profile for SAB-142, characterized as not causing serum sickness or anti-drug antibodies at the target dose.
“We are excited to share data at another major international conference to highlight the robust multi-specific mechanism of action of our lead program, SAB-142. Our presentations at ATTD-Asia continue to support the development of SAB-142 as a potential best-in-class immunotherapy, currently in Phase 2b clinical development for delaying the progression of T1D in new-onset, Stage 3 patients,” said Alexandra Kropotova, M.D., MBA, Chief Medical Officer, SAB BIO. “We look forward to sharing additional Phase 1 data and dosing the first patient in the Phase 2b SAFEGUARD clinical trial later this year.”
Oral Presentation Details:
Title
:
Mechanism of Action of a Fully Human Anti-Thymocyte Globulin, SAB-142, for the Treatment of Type 1 Diabetes
Session:
0730 – Orals 01: Pharmacotherapy and Safety, Drugs and Biologics | Presentation ID 21
Presenter:
Christoph Bausch, PhD, EVP and COO, SAB BIO
Presentation Date and Time:
Wednesday, December 10, 2025 | 17:00 - 17:12 SGT
Location:
Room 326
Oral E-Poster Presentation Details:
Title
:
Immunomodulation without Sustained Lymphodepletion: SAB-142, a Fully Human Anti-Thymocyte Globulin
Session:
0650 – Short Oral 07: New Medications for Treating Obesity and Diabetes Part II | Presentation ID 94
Presenter:
Stan Stoyanov, MD, VP, Clinical Development, SAB BIO
Presentation Date and Time:
Wednesday, December 10, 2025 | 17:25 - 17:30 SGT
Location:
Station 1
Title
:
Safety Profile of SAB-142; A Fully Human Anti-Thymocyte Globulin
Session:
0650 - Short Oral 07: New Medications for Treating Obesity and Diabetes Part II | Presentation ID 94
Presenter:
Stan Stoyanov, MD, VP, Clinical Development, SAB BIO
Presentation Date and Time:
Wednesday, December 10, 2025| 15:35 - 15:40 SGT
Location:
Station 1
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 like cytotoxic T-cells. 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. 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. 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. For more information, visit
www.sab.bio
.
Forward-Looking Statements
Certain statements made in this current report 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:
Cristi Barnett
[email protected]
Media:
Sheila Carlson
[email protected]