Shattuck Labs announces upcoming milestones for SL-325, a novel antibody targeting inflammatory diseases, with key presentations and funding plans outlined.
Quiver AI Summary
Shattuck Labs, Inc. has announced a corporate update highlighting significant milestones and expectations for 2025 regarding its potential first-in-class DR3 blocking antibody, SL-325, aimed at treating inflammatory and immune-related diseases. CEO Dr. Taylor Schreiber expressed optimism about SL-325’s ability to effectively block the DR3/TL1A signaling pathway based on preclinical studies, with a Phase 1 clinical trial set to commence later in the year. Key upcoming events include presentations at two notable congresses in February 2025 and participation in the J.P. Morgan Healthcare Conference in January 2025. Financially, Shattuck reported approximately $90.1 million in cash and equivalents, sufficient to fund operations into 2027. The press release outlines the timeline for critical studies and regulatory filings for SL-325, emphasizing the company's commitment to developing innovative treatments for autoimmune diseases.
Potential Positives
- Shattuck Labs is progressing toward a Phase 1 clinical trial for its lead product, SL-325, with initiation expected in the third quarter of 2025, indicating a timeline for advancing its drug development.
- The company has been selected to present data at prominent scientific congresses, including an oral presentation at the European Crohn’s and Colitis Organization Congress, highlighting its research credibility and visibility in the scientific community.
- Shattuck Labs reported a strong cash position of approximately $90.1 million, which is expected to fund operations into 2027, providing financial stability for ongoing and future projects.
- SL-325 is described as a potential first-in-class antibody targeting the DR3/TL1A signaling pathway, suggesting significant innovation and possible competitive advantage in the treatment of inflammatory diseases.
Potential Negatives
- The press release heavily relies on forward-looking statements, which come with inherent risks and uncertainties that could lead to actual results differing markedly from projections.
- The company is still in the preclinical phase for SL-325, meaning it has not yet proven the drug's safety and efficacy in humans, which can create skepticism among investors and stakeholders.
- While the company claims sufficient funds to operate until 2027, its reliance on future fundraising and potential regulatory approvals poses a significant risk to its financial health and operational viability.
FAQ
What is SL-325 and how does it work?
SL-325 is a first-in-class DR3 antagonist antibody aiming to block the TL1A/DR3 signaling pathway for better treatment outcomes.
When will the SL-325 Phase 1 clinical trial begin?
The Phase 1 clinical trial for SL-325 is expected to initiate in the third quarter of 2025.
What key milestones are anticipated for Shattuck Labs in 2025?
Key milestones include preclinical readouts, IND filing, and clinical trial initiation for SL-325.
Where will Shattuck Labs present its research data?
Shattuck Labs will present at the Crohn’s and Colitis Congress and the European Crohn’s and Colitis Organization Congress in 2025.
What is the current cash position of Shattuck Labs?
As of September 30, 2024, Shattuck has approximately $90.1 million in cash and equivalents, funding operations into 2027.
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.
$STTK Insider Trading Activity
$STTK insiders have traded $STTK stock on the open market 3 times in the past 6 months. Of those trades, 2 have been purchases and 1 have been sales.
Here’s a breakdown of recent trading of $STTK stock by insiders over the last 6 months:
- GROUP, LLC REDMILE has traded it 2 times. They made 1 purchase, buying 133,371 shares and 1 sale, selling 133,371 shares.
- TAYLOR SCHREIBER (Chief Executive Officer) purchased 36,500 shares.
To track insider transactions, check out Quiver Quantitative's insider trading dashboard.
$STTK Hedge Fund Activity
We have seen 43 institutional investors add shares of $STTK stock to their portfolio, and 26 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- PROSIGHT MANAGEMENT, LP added 1,008,726 shares (+21.6%) to their portfolio in Q3 2024
- TWO SIGMA ADVISERS, LP added 217,700 shares (+601.4%) to their portfolio in Q3 2024
- NORTHERN TRUST CORP added 216,203 shares (+201.0%) to their portfolio in Q3 2024
- UBS GROUP AG added 212,905 shares (+1795.0%) to their portfolio in Q3 2024
- ADAGE CAPITAL PARTNERS GP, L.L.C. added 155,000 shares (+5.6%) to their portfolio in Q3 2024
- PINNACLE ASSOCIATES LTD removed 141,977 shares (-23.7%) from their portfolio in Q3 2024
- RENAISSANCE TECHNOLOGIES LLC removed 141,410 shares (-36.1%) from their portfolio in Q3 2024
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
Full Release
AUSTIN, TX and DURHAM, NC, Jan. 02, 2025 (GLOBE NEWSWIRE) -- Shattuck Labs, Inc. (Shattuck) (NASDAQ: STTK), a biotechnology company pioneering the development of novel therapeutics targeting tumor necrosis factor (TNF) superfamily receptors for the treatment of patients with inflammatory and immune-related diseases, today announced a corporate update and highlighted upcoming key milestones anticipated in 2025.
“We have made considerable progress in the development of our potential first-in-class DR3 blocking antibody, SL-325,” said Taylor Schreiber, M.D., Ph.D., Chief Executive Officer of Shattuck. “Based on observations from our preclinical, non-human primate (NHP) studies, we remain highly optimistic that SL-325 will achieve a more complete blockade of the clinically validated DR3/TL1A signaling pathway and are excited to be selected to present these data as an oral presentation at the upcoming European Crohn’s and Colitis Organization Congress. Our phase 1 clinical trial for SL-325 is expected to begin later this year, and we believe we are well-positioned to use resources efficiently to fund operations into 2027.”
DR3 Program Milestones Expected in 2025
- Preclinical SL-325 data readout from GLP toxicology study in NHPs expected in the first quarter of 2025.
- IND filing for SL-325 expected in the third quarter of 2025.
- SL-325 Phase 1 clinical trial initiation expected in the third quarter of 2025.
- Nomination of lead DR3 bispecific development candidate(s) anticipated in the second half of 2025.
Upcoming Scientific Presentations
- Abstract accepted for poster presentation at the upcoming Crohn’s and Colitis Congress , to be held February 6–8, 2025 in San Francisco, CA.
- Abstract accepted for oral presentation at the upcoming 20th European Crohn’s and Colitis Organization Congress , to be held February 19–22, 2025 in Berlin, Germany.
Upcoming Investor Conference Presentation
-
43
rd
Annual J.P. Morgan Healthcare Conference (San Francisco, CA), January 13–16, 2025.
- Format: Dr. Taylor Schreiber, M.D., Ph.D., Shattuck’s Chief Executive Officer, will present the Company’s Corporate Presentation and participate in scheduled one-on-one investor meetings.
- Date/Time: January 16, 2025, at 7:00 a.m. PT.
- Location: The Westin St. Francis, San Francisco, California
-
A live webcast of the presentations will be available on the
Events and Presentations
section of the Company’s website. A replay of the webcast will be archived for up to 30 days following the presentation date.
Cash Position and Financial Guidance
As of September 30, 2024, cash and cash equivalents and investments were approximately $90.1 million. Shattuck believes its cash and cash equivalents and investments will be sufficient to fund its planned operations into 2027, beyond results from its Phase 1 clinical trial of SL-325.
About SL-325
SL-325 is a first-in-class Death Receptor 3 (DR3) antagonist antibody designed to achieve a more complete blockade of the clinically validated TL1A/DR3 pathway. Shattuck’s preclinical studies demonstrate high affinity binding, superior efficacy over TL1A antibodies, and offer a data-driven rationale for targeting the TNF receptor, DR3, versus its ligand, TL1A. SL-325 is currently being evaluated in a GLP toxicology study in non-human primates, with an IND filing expected in the third quarter of 2025.
About Shattuck Labs, Inc.
Shattuck Labs, Inc. (Nasdaq: STTK) is a biotechnology company specializing in the development of potential treatments for autoimmune/inflammatory diseases. The Company is developing a potentially first-in-class antibody for the treatment of inflammatory bowel disease (IBD) and other inflammatory autoimmune diseases. Shattuck’s expertise in protein engineering and the development of novel TNF receptor agonist and antagonist therapeutics come together in its lead program, SL-325, a first-in-class DR3 antagonist antibody designed to achieve a more complete blockade of the clinically validated TL1A/DR3 pathway. The Company has offices in both Austin, Texas and Durham, North Carolina. For more information, please visit: www.ShattuckLabs.com .
Forward-Looking Statements
Certain statements in this press release may constitute “forward-looking statements” within the meaning of the federal securities laws, including, but not limited to, our expectations regarding: plans for our preclinical studies, clinical trials and research and development programs, particularly with respect to SL-325; the anticipated timing of any regulatory filings for SL-325; the anticipated timing of our preclinical studies and clinical trials for SL-325; the clinical benefit, safety and tolerability of SL-325; and expectations regarding the time period over which our capital resources will be sufficient to fund our anticipated operations. Words such as “may,” “might,” “will,” “objective,” “intend,” “should,” “could,” “can,” “would,” “expect,” “believe,” “design,” “estimate,” “predict,” “potential,” “develop,” “plan” or the negative of these terms, and similar expressions, or statements regarding intent, belief, or current expectations, are forward-looking statements. While we believe these forward-looking statements are reasonable, undue reliance should not be placed on any such forward-looking statements, which are based on information available to us on the date of this release. These forward-looking statements are based upon current estimates and assumptions and are subject to various risks and uncertainties (including, without limitation, those set forth in our filings with the U.S. Securities and Exchange Commission (SEC)), many of which are beyond our control and subject to change. Actual results could be materially different. Risks and uncertainties include: global macroeconomic conditions and related volatility, expectations regarding the initiation, progress, and expected results of our preclinical studies, clinical trials and research and development programs; expectations regarding the timing, completion and outcome of our clinical trials; the unpredictable relationship between preclinical study results and clinical study results; the timing or likelihood of regulatory filings and approvals; our expectations regarding the overall benefit of the strategic prioritization of our pipeline; liquidity and capital resources; and other risks and uncertainties identified in our Annual Report on Form 10-K for the year ended December 31, 2023, and subsequent disclosure documents filed with the SEC. We claim the protection of the Safe Harbor contained in the Private Securities Litigation Reform Act of 1995 for forward-looking statements. We expressly disclaim any obligation to update or alter any statements whether as a result of new information, future events or otherwise, except as required by law.
The Company intends to use the investor relations portion of its website as a means of disclosing material non-public information and for complying with disclosure obligations under Regulation FD.
Investor & Media Contact:
Conor Richardson
Vice President of Investor Relations
Shattuck Labs, Inc.
[email protected]