Form 8-K

8-K — Shattuck Labs, Inc.

Accession: 0001193125-26-263831

Filed: 2026-06-09

Period: 2026-06-08

CIK: 0001680367

SIC: 2834 (PHARMACEUTICAL PREPARATIONS)

Item: Regulation FD Disclosure

Item: Other Events

Item: Financial Statements and Exhibits

Documents

8-K — d120796d8k.htm (Primary)

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8-K

8-K (Primary)

Filename: d120796d8k.htm · Sequence: 1

8-K

false 0001680367 0001680367 2026-06-08 2026-06-08

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, DC 20549

FORM 8-K

CURRENT REPORT

Pursuant to Section 13 or 15(d)

of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): June 8, 2026

Shattuck Labs, Inc.

(Exact name of registrant as specified in its charter)

Delaware

001-39593

81-2575858

(State or other jurisdiction of

incorporation or organization)

(Commission

File Number)

(I.R.S. Employer

Identification Number)

500 W. 5th Street, Suite 1200

Austin, TX 78701

(Address of principal executive offices, including zip code)

(512) 900-4690

(Registrant’s telephone number, including area code)

Not Applicable

(Former name or former address, if changed since last report)

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

☐

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

☐

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

☐

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

☐

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

Trading

Symbol(s)

Name of each exchange

on which registered

Common Stock, par value $0.0001 per share

STTK

The Nasdaq Global Select Market

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging Growth Company ☐

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

Item 7.01

Regulation FD Disclosure.

On June 8, 2026, Shattuck Labs, Inc. (the “Company” or “Shattuck”) issued a press release announcing data from its Phase 1 clinical trial of SL-325, its lead DR3 blocking antibody. The Company hosted an investor call and webcast, during which it described additional expected data readouts and milestones for 2026, including (i) initiation of RECEPTIVE-CD1 Phase 2b trial of SL-325 in Crohn’s disease, expected in the third quarter of 2026 and (ii) IND filing for SL-846 (DR3xIL-23R bispecific), which is expected in the first half of 2027.

A copy of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K and is incorporated by reference herein. The exhibit furnished under Item 7.01 of this Current Report on Form 8-K shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall they be deemed incorporated by reference in any filing under the Exchange Act or the Securities Act of 1933, as amended, regardless of any general incorporation language in such filing.

Item 8.01

Other Events.

Data Release

On June 8, 2026, the Company released its presentation on data from its Phase 1 clinical trial of SL-325.

Key Phase 1 Findings

The Phase 1 trial is a first-in-human, randomized, placebo-controlled trial evaluating the safety, tolerability, pharmacokinetics (“PK”), receptor occupancy (“RO”), pharmacodynamics (“PD”), and immunogenicity of SL-325 in healthy volunteers. The study enrolled 72 participants, across six single-ascending dose cohorts, with doses ranging from 0.1 mg/kg to 30.0 mg/kg, and three multiple-ascending dose cohorts, with doses ranging from 1 mg/kg to 10 mg/kg.

•

Immunogenicity: Antidrug antibodies (“ADA”) to SL-325 were detected in 3.7% [2/54] of participants who received SL-325.

•

In these two participants, ADA were low titer (≤16), and no impact to PK or receptor occupancy was observed.

•

The ADA assay used to detect ADA to SL-325 has a sensitivity of 5.0 ng/ml and drug tolerance of up to SL-325 concentrations of 160.0 µg/ml in the serum. For each participant in this Phase 1 trial, samples were analyzed over a time course, ensuring that samples from each participant fell within the dynamic range of the assay across the full dose range, and thus limiting the possibility of false negative results.

•

Published and emerging data suggest that ADA to anti-TL1A antibodies impact efficacy. SL-325’s potentially best-in-mechanism immunogenicity profile is expected to lead to improved efficacy at both the induction and maintenance timepoints compared to anti-TL1A antibodies.

•

Pharmacokinetics and Receptor Occupancy:

•

Complete DR3 occupancy, as measured by blockade of TL1A binding, was observed at doses of 0.1 mg/kg and higher in all participants.

•

Complete inhibition of TL1A binding was durable for more than 10 weeks, and extended PK modeling suggests that complete inhibition of TL1A binding may be sustained for greater than 3 months at doses of greater than1 mg/kg of SL-325.

•

The PK profile of SL-325 demonstrated proportional increases in Cmax and AUClast across all dose levels.

•

Repeated dosing demonstrated an accumulation ratio of 1.64-1.75.

•

A subcutaneous formulation of SL-325 has been developed. These Phase 1 results indicate the potential for quarterly dosing at a volume compatible with an autoinjector pen.

•

Pharmacodynamics: Clinical data now corroborate our previous preclinical findings that SL-325 is a pure DR3 blocking antibody.

•

No evidence of DR3 agonism was observed.

•

No evidence of SL-325 mediated lymphocyte proliferation or changes in serum cytokines was observed in any participant at any dose level.

•

No increases in serum levels of TL1A from baseline were observed.

•

Safety: SL-325 was well tolerated at all dose levels and upon repeat dosing, with a favorable safety profile consistent with the TL1A inhibitor class.

•

There were no serious treatment-emergent adverse events (“TEAEs”) or serious adverse events.

•

All treatment-related adverse events (“TRAEs”) were Grade 1. TRAEs were observed in 12 participants.

RECEPTIVE-CD1 Phase 2b Trial of SL-325 in Crohn’s Disease

The RECEPTIVE-CD1 clinical trial is designed as a randomized, double-blind, placebo-controlled Phase 2b clinical trial to evaluate the safety and efficacy of two dose levels of SL-325 as monotherapy versus placebo in moderate-to-severe Crohn’s disease. SL-325 will be administered intravenously, and the trial will include a 12-week induction period, followed by a 40-week maintenance period, for a total of 52 weeks of treatment for each patient enrolled.

•

RECEPTIVE-CD1 is expected to enroll approximately 174 patients, randomized 1:1:1, with patients receiving either low dose SL-325, high dose SL-325, or placebo. RECEPTIVE-CD1 will enroll patients at clinical sites in the United States, Canada, and Europe.

•

RECEPTIVE-CD1 is expected to enroll patients with moderate-to-severe Crohn’s disease, as defined with a Crohn’s Disease Activity Index (“CDAI”) score of between 220 and 450.

•

The primary endpoint is expected to be endoscopic response at Week 12, and the key secondary endpoint will be clinical remission at Week 12.

•

Patients randomized to the placebo arm will be eligible to receive SL-325 after the 12-week induction period.

•

The primary endpoint, endoscopic response at 12 weeks, is expected to be disclosed in the first half of 2028.

SL-846: A Dual DR3 and IL-23 Receptor Blocking Antibody

SL-846 is Shattuck’s lead bispecific product candidate and is designed to simultaneously bind to DR3 and to IL-23 receptor, blocking the interaction with TL1A and IL-23, respectively, while avoiding the risk of immune complex formation and resulting ADA challenges of the TL1A-based bispecifics.

•

SL-846 is an Fc-silenced, half-life extended, IgG1 bispecific antibody.

•

Preclinical data demonstrated that SL-846 was equipotent, or more potent, than sequence equivalents of risankizumab and icotrokinra controls in multiple in vitro and cell-based potency assays.

•

SL-846 is currently being evaluated in an ongoing IND-enabling GLP toxicology study in non-human primates. Safety and immunogenicity data are expected in the second half of 2026.

•

Shattuck expects to submit an IND for SL-846 in the first half of 2027.

The Company also released its data presentation, which supersedes prior content of the same nature in previously published presentations and which is attached hereto as Exhibit 99.3 and is incorporated by reference in this Item 8.01.

Warrant Exercises

On June 9, 2026, the Company announced that it had received notices to exercise an aggregate of approximately 50.6 million outstanding common stock warrants, representing approximately 96% of the warrants issued in the Company’s August 4, 2025 private placement. As of March 31, 2026, the Company had received aggregate gross proceeds of approximately $5.6 million from the exercise of 5,147,773 warrants and expects to receive additional aggregate gross proceeds of approximately $49.3 million from the exercise of an additional 45,438,709 warrants. A copy of the press release announcing the warrant exercises is attached as Exhibit 99.2 to this Current Report on Form 8-K and is incorporated herein by reference.

Item 9.01

Financial Statements and Exhibits.

(d) Exhibits. The following exhibits are being furnished herewith:

EXHIBIT INDEX

Exhibit

No.

Description

99.1

Press Release, dated June 8, 2026

99.2

Press Release, dated June 9, 2026

99.3

Data Presentation, dated June 8, 2026

104

Cover Page Interactive Data File (embedded within the Inline XBRL document).

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

Shattuck Labs, Inc.

Date: June 9, 2026

By:

/s/ Taylor Schreiber

Dr. Taylor Schreiber

Chief Executive Officer

(principal executive officer)

EX-99.1

Filename: d120796dex991.htm · Sequence: 2

EX-99.1

Exhibit 99.1

Shattuck Labs Announces Phase 1 Results for SL-325

•

Potentially best-in-mechanism

immunogenicity profile, with only 3.7% of participants developing antidrug antibodies

•

Complete blockade of TL1A binding to DR3 for over 3 months expected at doses of 1 mg/kg and higher

•

Well tolerated with a favorable safety profile consistent with the TL1A inhibitor class

•

No evidence of DR3 agonism

•

RECEPTIVE-CD1 Phase 2b clinical trial in patients with Crohn’s

disease expected to initiate in the third quarter of 2026

•

Lead bispecific product candidate, SL-846 (DR3xIL-23R), currently being evaluated in IND-enabling toxicology studies; Phase 1 initiation expected in the first half of 2027

AUSTIN, TX and DURHAM, NC, June 8, 2026 – Shattuck Labs, Inc. (Shattuck or the Company) (NASDAQ: STTK), a clinical-stage

biotechnology company pioneering the development of potential first-in-class monoclonal and bispecific DR3 blocking antibodies for the treatment of patients with

inflammatory and immune-mediated diseases, today announced data from its Phase 1 clinical trial of SL-325, Shattuck’s lead DR3 blocking antibody candidate.

“SL-325 is now the first antibody that blocks the receptor for TL1A, known as DR3, to generate human clinical

data. The profile of SL-325 is highly encouraging, including a potentially best-in-mechanism immunogenicity profile, saturation

of DR3 at low doses of SL-325, and durable inhibition of TL1A binding for months after a single dose.” said Taylor Schreiber, M.D., Ph.D., Chief Executive Officer of Shattuck. “These data indicate

that blocking DR3 with SL-325, or with our DR3 by IL-23 receptor blocking bispecific antibody candidate, SL-846, may

substantially improve upon the efficacy shown to date with the TL1A inhibitor class, providing an opportunity to maximize potential efficacy for TL1A blockade in IBD and beyond.”

Key Phase 1 Findings

The Phase 1 trial is a first-in-human, randomized, placebo-controlled trial evaluating the safety, tolerability, pharmacokinetics (“PK”), receptor occupancy (“RO”),

pharmacodynamics (“PD”), and immunogenicity of SL-325 in healthy volunteers. The study enrolled 72 participants, across six single-ascending dose cohorts, with doses ranging from 0.1 mg/kg to 30.0

mg/kg, and three multiple-ascending dose cohorts, with doses ranging from 1 mg/kg to 10 mg/kg.

•

Immunogenicity: Antidrug antibodies (“ADA”) to SL-325

were detected in 3.7% [2/54] of participants who received SL-325.

•

In these two participants, ADA were low titer (≤16), and no impact to PK or receptor occupancy was

observed.

•

The ADA assay used to detect ADA to SL-325 has a sensitivity of 5.0 ng/ml

and drug tolerance of up to SL-325 concentrations of 160.0 µg/ml in the serum. For each participant in this Phase 1 trial, samples were analyzed over a time course, ensuring that samples from each

participant fell within the dynamic range of the assay across the full dose range, and thus limiting the possibility of false negative results.

•

maintenance timepoints compared to anti-TL1A antibodies.

•

Pharmacokinetics and Receptor Occupancy:

•

Complete DR3 occupancy, as measured by blockade of TL1A binding, was observed at doses of 0.1 mg/kg and higher in

all participants.

•

Complete inhibition of TL1A binding was durable for more than 10 weeks, and extended PK modeling suggests that

complete inhibition of TL1A binding may be sustained for greater than 3 months at doses of greater than1 mg/kg of SL-325.

•

The PK profile of SL-325 demonstrated proportional increases in Cmax and

AUClast across all dose levels.

•

Repeated dosing demonstrated an accumulation ratio of 1.64-1.75.

•

A subcutaneous formulation of SL-325 has been developed. These Phase 1

results indicate the potential for quarterly dosing at a volume compatible with an autoinjector pen.

•

Pharmacodynamics: Clinical data now corroborate our previous preclinical findings that SL-325 is a pure DR3 blocking antibody.

•

No evidence of DR3 agonism was observed.

•

No evidence of SL-325 mediated lymphocyte proliferation or changes in

serum cytokines was observed in any participant at any dose level.

•

No increases in serum levels of TL1A from baseline were observed.

•

Safety: SL-325 was well tolerated at all dose levels and upon

repeat dosing, with a favorable safety profile consistent with the TL1A inhibitor class.

•

There were no serious treatment-emergent adverse events (“TEAEs”) or serious adverse events.

•

All treatment-related adverse events (“TRAEs”) were Grade 1. TRAEs were observed in 12 participants.

RECEPTIVE-CD1 Phase 2b Trial of SL-325 in

Crohn’s Disease

The RECEPTIVE-CD1 clinical trial is designed as a randomized, double-blind,

placebo-controlled Phase 2b clinical trial to evaluate the safety and efficacy of two dose levels of SL-325 as monotherapy versus placebo in

moderate-to-severe Crohn’s disease. SL-325 will be administered intravenously, and the trial will include a 12-week induction period, followed by a 40-week maintenance period, for a total of 52 weeks of treatment for each patient enrolled.

•

RECEPTIVE-CD1 is expected to enroll approximately 174 patients,

randomized 1:1:1, with patients receiving either low dose SL-325, high dose SL-325, or placebo. RECEPTIVE-CD1 will enroll

patients at clinical sites in the United States, Canada, and Europe.

•

RECEPTIVE-CD1 is expected to enroll patients with moderate-to-severe Crohn’s disease, as defined with a Crohn’s Disease Activity Index (“CDAI”) score of between 220 and 450.

•

The primary endpoint is expected to be endoscopic response at Week 12, and the key secondary endpoint will be

clinical remission at Week 12.

•

Patients randomized to the placebo arm will be eligible to receive SL-325

after the 12-week induction period.

•

The primary endpoint, endoscopic response at 12 weeks, is expected to be disclosed in the first half of 2028.

SL-846: A Dual DR3 and IL-23 Receptor Blocking

Antibody

SL-846 is Shattuck’s lead bispecific product candidate and is designed to simultaneously bind

to DR3 and to IL-23 receptor, blocking the interaction with TL1A and IL-23, respectively, while avoiding the risk of immune complex formation and resulting ADA

challenges of the TL1A-based bispecifics.

•

SL-846 is an Fc-silenced,

half-life extended, IgG1 bispecific antibody.

•

Preclinical data demonstrated that SL-846 was equipotent, or more potent,

than sequence equivalents of risankizumab and icotrokinra controls in multiple in vitro and cell-based potency assays.

•

SL-846 is currently being evaluated in an ongoing IND-enabling GLP toxicology study in non-human primates. Safety and immunogenicity data are expected in the second half of 2026.

•

Shattuck expects to submit an IND for SL-846 in the first half of 2027.

About SL-325

SL-325 is a potentially first-in-class

Death Receptor 3 (DR3) blocking antibody designed to achieve a complete and durable blockade of the clinically validated DR3/TL1A pathway. Shattuck’s preclinical studies demonstrate high affinity binding and superior activity over TL1A

antibodies, and offer a data-driven rationale for targeting the TNF receptor, DR3, versus its ligand, TL1A. SL-325 is a fully Fc-silenced, fully human immunoglobulin G

monoclonal antibody with a favorable safety profile, potentially best-in-mechanism immunogenicity profile, no evidence of residual DR3 agonism capable of providing

durable blockade of TL1A binding to DR3 at low doses in a recently completed Phase 1 clinical trial. SL-325 is expected to be evaluated in a Phase 2b clinical trial in Crohn’s Disease patients initiating

in the third quarter of 2026.

About SL-846

SL-846 is a potentially first-in-class

Death Receptor 3 (DR3) by IL-23 receptor (IL-23R) blocking bispecific antibody designed to achieve complete and durable blockade of the clinically validated DR3/TL1A and

IL-23/IL-23R pathways. Shattuck’s preclinical studies demonstrate high affinity binding to both DR3 and IL-23R, with

equivalent or superior in vitro potency in comparison to benchmark IL-23 controls (sequence equivalents of risankizumab and icotrokinra) in a variety of preclinical assays. SL-846 is an Fc-silenced, half-life extended, fully human immunoglobulin G bispecific antibody currently being evaluated for safety, tolerability, immunogenicity, and

pharmacodynamics in an IND-enabling GLP toxicology study in non-human primates.

About Shattuck Labs, Inc.

Shattuck Labs, Inc. is a

clinical-stage biotechnology company pioneering the development of potentially first-in-class monoclonal and bispecific DR3 blocking antibodies for the treatment of

patients with inflammatory and immune-mediated diseases. Shattuck’s expertise in protein engineering and the development of novel TNF receptor therapeutics come together in its lead program, SL-325, a

potentially first-in-class DR3 antagonist antibody designed to achieve a more complete blockade of the clinically validated DR3/TL1A 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, Shattuck’s expectations regarding: plans for its preclinical studies, clinical trials and research and development programs, particularly with respect to SL-325; the anticipated

timing of release of data from the Company’s ongoing Phase 1 clinical trial of SL-325; the anticipated timing of initiation of a Phase 2 clinical trial of SL-325

in patients with Crohn’s disease; the clinical benefit, safety and tolerability of SL-325; anticipated development of additional preclinical pipeline candidates; the timing of nomination, release of

preclinical data and development timelines of a lead bispecific antibody candidate; and expectations regarding the time period over which the Company’s capital resources will be sufficient to fund its 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 the Company believes 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 it 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 Shattuck’s filings with the U.S.

Securities and Exchange Commission (SEC)), many of which are beyond its 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 the Company’s preclinical studies, clinical trials and research and development programs; expectations regarding the timing, completion and outcome of the Company’s

preclinical studies and clinical trials; the unpredictable relationship between preclinical study results and clinical study results; the timing or likelihood of regulatory filings and approvals; liquidity and capital resources, including the time

period over which current capital resources are expected to the fund the Company’s operations; and other risks and uncertainties identified in Shattuck’s Annual Report on Form 10-K for the year

ended December 31, 2025, and subsequent disclosure documents filed with the SEC. Shattuck claims the protection of the Safe Harbor contained in the Private Securities Litigation Reform Act of 1995 for forward-looking statements. The Company

expressly disclaims 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:

Andrew R. Neill

Chief Financial Officer

Shattuck Labs, Inc.

InvestorRelations@shattucklabs.com

EX-99.2

Filename: d120796dex992.htm · Sequence: 3

EX-99.2

Exhibit 99.2

Shattuck Labs Announces Exercise of Outstanding Common Stock Warrants and Provides Financial Update

AUSTIN, Texas and DURHAM, N.C., June 9, 2026 (GLOBE NEWSWIRE) — Shattuck Labs, Inc. (Shattuck) (NASDAQ: STTK), a clinical-stage

biotechnology company pioneering the development of potentially first-in-class monoclonal and bispecific DR3-blocking antibodies

for the treatment of patients with inflammatory and immune-mediated diseases, today announced it has received notices to exercise totaling approximately 50.6 million common stock warrants to date, representing approximately 96% of the warrants

issued in the Company’s August 4, 2025 private placement. The exercise of these warrants is expected to result in aggregate gross proceeds of approximately $54.9 million. As of March 31, 2026, the Company had received aggregate

gross proceeds of approximately $5.6 million pursuant to the exercise of 5,147,773 warrants. The Company expects to receive additional aggregate gross proceeds totaling approximately $49.3 million from the exercise of 45,438,709 common

stock warrants since March 31, 2026. Together with existing cash and cash equivalents and short term investments of approximately $90.4 million as of March 31, 2026, Shattuck expects to be able to fund operations into 2029. This cash

runway guidance is based on the Company’s current operational plans and excludes any additional capital that may be received (other than from the exercise of these common stock warrants), proceeds from business development transactions, and/or

additional costs associated with clinical development activities that may be undertaken.

About Shattuck Labs, Inc.

Shattuck Labs, Inc. is a clinical-stage biotechnology company pioneering the development of potentially first-in-class monoclonal and bispecific DR3 blocking antibodies for the treatment of patients with inflammatory and immune-mediated diseases. Shattuck’s expertise in protein engineering and the

development of novel TNF receptor therapeutics come together in its lead program, SL-325, a potentially first-in-class DR3

antagonist antibody designed to achieve a more complete blockade of the clinically validated DR3/TL1A 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, Shattuck’s expectations regarding: plans for its preclinical studies, clinical trials and

research and development programs, particularly with respect to SL-325; the anticipated timing of initiation of a Phase 2 clinical trial of SL-325 in patients with

Crohn’s disease; the clinical benefit, safety and tolerability of SL-325; anticipated development of additional preclinical pipeline candidates; the timing of nomination, release of preclinical data and

development timelines of a lead bispecific antibody candidate; and expectations regarding the time period over which the Company’s capital resources will be sufficient to fund its 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 the Company believes 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 it 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 Shattuck’s filings with the U.S. Securities and

Exchange Commission (SEC)), many of which are beyond its 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 the Company’s preclinical studies, clinical trials and research and development programs; expectations regarding the timing, completion and outcome

of the Company’s preclinical studies and clinical trials; the unpredictable relationship between preclinical study results and clinical study results; the timing or likelihood of regulatory

filings and approvals; liquidity and capital resources, including the time period over which current capital resources are expected to the fund the Company’s operations; and other risks and uncertainties identified in Shattuck’s Annual

Report on Form 10-K for the year ended December 31, 2025, and subsequent disclosure documents filed with the SEC. Shattuck claims the protection of the Safe Harbor contained in the Private Securities

Litigation Reform Act of 1995 for forward-looking statements. The Company expressly disclaims any intention 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:

Andrew R. Neill

Chief Financial Officer

Shattuck Labs, Inc.

InvestorRelations@shattucklabs.com

EX-99.3

Filename: d120796dex993.htm · Sequence: 4

EX-99.3

Phase 1 Clinical Data of SL-325, a

Potentially First-In-Class DR3 Blocking Antibody & Pipeline Update SHATTUCK LABS, INC. NASDAQ: STTK Exhibit 99.3

Disclaimer This presentation contains

“forward-looking statements” within the meaning of the federal securities laws, which statements are subject to substantial risks and uncertainties and are based on our estimates and assumptions. All statements, other than statements of

historical facts included in this presentation, are forward-looking statements, including statements, express or implied, concerning: our plans, objectives, goals, strategies or intentions relating to products and markets; whether the common stock

warrants will be exercised and provide us with additional capital; the use of proceeds from the private placement; the potential purity, potency, safety, and clinical benefits of our product candidates, including SL-325; the anticipated timing and

design of our planned and ongoing preclinical studies and clinical trials, including timing of enrollment; the anticipated timing for data and the association of preclinical data with potential clinical benefit; the timing of anticipated milestones,

plans and objectives of management for future operations; the anticipated development of additional preclinical pipeline programs; potential addressable market size; and our expectations regarding the time period over which our capital resources

will be sufficient to fund our anticipated operations. In some cases, you can identify forward-looking statements by terms such as “may,” “might,” “will,” “objective,” “intend,”

“should,” “could,” “can,” “would,” “expect,” “believe,” “design,” “estimate,” “predict,” “potential,” “plan,”

“develop” or the negative of these terms, and similar expressions intended to identify forward-looking statements. These statements involve known and unknown risks, uncertainties and other factors that could cause our actual results to

differ materially from the forward-looking statements expressed or implied in this presentation, in addition to those risks and uncertainties, such as 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 described in “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations” in our Annual Report on Form 10-K (File No. 001-39593) for the fiscal year ended

December 31, 2025 and elsewhere in such filing and in our other periodic reports and subsequent disclosure documents filed with the U.S. Securities and Exchange Commission. We cannot assure you that we will realize the results, benefits or

developments that we expect or anticipate or, even if substantially realized, that they will result in the consequences or affect us or our business in the way expected. Forward-looking statements are not historical facts, and reflect our current

views with respect to future events. Given the significant uncertainties, you should evaluate all forward-looking statements made in this presentation in the context of these risks and uncertainties and not place undue reliance on these

forward-looking statements as predictions of future events. All forward-looking statements in this presentation apply only as of the date made and are expressly qualified in their entirety by the cautionary statements included in this presentation.

We have no intention to publicly update or revise any forward-looking statements to reflect subsequent events or circumstances, except as required by law. We obtained the data used throughout this presentation from our own internal estimates and

research, as well as from research, surveys and studies conducted by third parties. Internal estimates are derived from publicly available information released and our own internal research and experience, and are based on assumptions made by us

based on such data and our knowledge, which we believe to be reasonable. In addition, while we believe the data included in this presentation is reliable and based on reasonable assumptions, we have not independently verified any third-party

information, and all such data involve risks and uncertainties and are subject to change based on various factors. This presentation concerns a discussion of investigational drugs that are under preclinical and/or clinical investigation and which

have not yet been approved for marketing by the U.S. Food and Drug Administration. They are currently limited by Federal law to investigational use, and no representations are made as to their safety or effectiveness for the purposes for which they

are being investigated.

Call Agenda and Participants SL-325

Phase 2b Study in Crohn’s Disease RECEPTIVE-CD1 Taylor Schreiber, MD, PhD Chief Executive Officer Lini Pandite, MD, MBA Chief Medical Officer Suresh De Silva, PhD Chief Scientific Officer Michael Choi, MD VP Clinical Development Andrew Neill,

MBA Chief Financial Officer All Closing and Q&A SL-846, A Potentially First-In-Class DR3 x IL-23R Bispecific Antibody SL-325 Phase 1 Results TL1A/DR3 Biology Potential Advantages of DR3 Blockade Introduction

Introduction SL-325 DR3 SL-325 is a

fully human, Fc-silenced, IgG1 monoclonal antibody (mAb) that selectively binds to DR3 and blocks its interaction with TL1A* DR3 blockade has the potential to provide superior efficacy in comparison to TL1A blockade because: DR3 is a more abundant

and stable target than TL1A Immunogenicity due to immune complex formation is not expected for SL-325 Phase 1 first-in-human trial evaluated the safety, tolerability, pharmacokinetics (PK), immunogenicity, and pharmacodynamic (PD) effects of SL-325

in healthy participants (NCT07158437) Key Findings Well tolerated across all dose levels, with a safety profile similar to those reported for anti-TL1A mAbs Prolonged blockade of TL1A binding at low doses may support quarterly maintenance

dosing intervals No evidence of DR3 agonism, confirming SL-325 is a pure DR3 blocking antibody Potentially best-in-mechanism immunogenicity profile with ADA rate of 3.7% *Hussain M et al. IBD Journal 2026. In Press

Bamias G. Gut 2025;74:652-668

Hussain M et al. IBD Journal 2026. In Press SL-325 Is a High-Affinity, Highly Specific, DR3 Blocking Antibody TL1A Is Primarily Expressed by Tissue-Resident APCs TL1A is the sole known signaling ligand for DR3 and does not signal through any other

receptors SL-325 potently inhibits TL1A binding to DR3 SL-325 does not bind DcR3, allowing TL1A clearance by DcR3 to remain intact SL-325 binds DR3 with very high affinity (1.3 pM) Highly durable blockade of TL1A binding is expected to extend

dosing intervals By targeting membrane-bound DR3 rather than soluble TL1A, SL-325 is designed to avoid circulating TL1A immune complex formation which leads to high ADA rates DR3 Is Primarily Expressed by Lymphoid Cells In Blood and

Tissue

Potentially First-in-Class Pipeline

Targeting DR3 IBD = Inflammatory Bowel Disease; RA = rheumatoid arthritis; PsA = psoriatic arthritis; HS = hidradenitis suppurativa, I&I = inflammatory and immune-mediated diseases Developing potentially first-in-class DR3 monospecific and

bispecific antibodies LEAD TARGET(S) INDICATIONS IND-ENABLING PHASE 1 PHASE 2 EXPECTED MILESTONES SL-325 DR3 IBD Potentially RA, PsA, HS, other I&I Phase 2b in Crohn’s disease Initiation in Q3 2026 Phase 2b in CD 12W Induction Data in 1H

2028 SL-425 EXTENDED HALF-LIFE DR3 Potentially RA, PsA, HS, other I&I SL-846 EXTENDED HALF-LIFE DR3 X IL-23R Potentially IBD, PsA, other I&I Phase 1 Initiation in 1H 2027 DR3 blockade with SL-325 provides potentially best-in-mechanism

immunogenicity compared to TL1A blocking antibodies Blocking DR3 may provide more potent inhibition of the TL1A/DR3 axis than TL1A blockade due to more durable inhibition of TL1A signaling

*Danese S et al. Lancet Gastroenterol

and Hepatol. 2025;10:882-895; SYRE Corp Update 6/17/2025; Balyan R et al. J Crohn‘s and Colitis 2024;18:1206-1207; RXDX Corp Update 12/7/2021; XNCR Corp Update 5/4/2026. **Emery P et al. Scand J Rheumatol 2020;49:361-370 Created in

https://BioRender.com Immune Complex Mediated Immunogenicity Limits Efficacy of TL1A Blocking Antibodies Anti-TL1A antibody binding to soluble TL1A in blood is an undesired site of action that causes immune complex formation This leads to anti-drug

antibody (ADA) rates for anti-TL1A antibodies of 48-100% in Phase 1 trials* Both total ADA and neutralizing ADA cause similar reduction in efficacy** ADA can accelerate clearance of TL1A blocking antibodies, which correlates with reduced

efficacy*

*Combined 450 mg and 900 mg dose

levels **50à50, 150à150 and 450à450 mg dose levels combined ***AT-IR patients Data in the figure are presented as a proportion of the total number of patients in remission at the maintenance timepoint relative to the induction

timepoint. Example for upadacitinib: 90 patients in remission in maintenance divided by 55 patients in remission at induction equates to an increase in the number of patients in remission from induction to maintenance of 38% High ADA May Limit

Durability of Clinical Benefit in IBD The mechanism of immune complex formation is similar for anti-TL1A and anti-TNF antibodies, leading to high rates of ADA to both classes ADA rates to IL-23 inhibitors are significantly lower than TL1A or TNF

inhibitors The number of patients in clinical remission improves over time for IBD drugs with low rates of ADA Placebo Adjusted Clinical Remission at Induction No. Patients in Remission Induction Maintenance Infliximab UC FDA Label 19.5% 161 160

Adalimumab UC Sandborn Gastro 2012, FDA Label 8.25% 41 43 Tulisokibart UC Ma C UEGW 2024 25% 18 19 Duvakitug UC* Teva Corp Updates 2/24/2025 & 2/19/2026 27% 39 37 Afimkibart UC Danese S, Lancet Gastro 2025** 20% 33 33 Upadacitinib UC Danese,

Lancet 2022 29% 58 80 Tofacitinib UC Sandborn, NEJM 2017, FDA Label 13% 55 90 Ustekinumab UC Sands, NEJM 2019, FDA Label 12% 41 79 Risankizumab UC Panaccione, J Crohn’s & Colitis 2025***, FDA Label 16% 38 90

Immune Complexes Between TL1A and

Anti-TL1A Antibodies Directly Increase TL1A Expression *Meylan et al. Immunity 2008; 29:79-89 **Data demonstrate fold increase in TL1A mRNA expression from human monocytes following exposure to the indicated test articles in vitro. Study conducted

by Shattuck. Study utilized a sequence-equivalent of tulisokibart. Created in https://BioRender.com Tulisokibart/TL1A immune complex (IC) triggers >75-fold increase in TL1A production by human monocytes in vitro** A feedback loop of TL1A immune

complexes increasing TL1A expression may: Further increase immunogenicity risk Increase the amount of antibody needed to neutralize free TL1A, potentially contributing to high dose requirements for TL1A antibodies

Phase 1 Clinical Trial of SL-325 in

Healthy Participants 0.1 mg/kg 1 mg/kg 0.3 mg/kg 3 mg/kg 1 mg/kg 10 mg/kg 3 mg/kg 10 mg/kg 30 mg/kg Single Ascending Dose PART B Multiple Ascending Dose (3 doses, q2w) Single ascending dose (SAD) and multiple ascending dose (MAD) study in healthy

participants Dosing is complete for all 72 participants Phase 1 Clinical Trial Design Key Questions Evaluated in Phase 1 Is SL-325 as well tolerated as anti-TL1A antibodies? Does human data confirm that SL-325 is a pure DR3 blocking antibody? How

durable is DR3 occupancy, and what does that translate to with regard to expected maintenance dosing intervals? Is SL-325 less immunogenic than TL1A blocking antibodies? INCREASING DOSE PART A 6 SL-325 : 2 Placebo Participants Per Cohort 6 SL-325 :

2 Placebo Participants Per Cohort Placebo SL-325 N 18 54 Median Age (years, range) 31 (21, 53) 35 (22, 54) Sex, % Female 56 69 Participant Demographics

TEAE = treatment emergent adverse

events; TRAE = treatment related or possibly related adverse events; IRR = infusion-related reaction *The participant experienced a mild IRR during the second infusion. The symptoms resolved without therapeutic intervention and

within 10 minutes. ADA remained negative. The participant was diagnosed with severe Strep throat the following day. The underlying medical condition may have contributed to the reaction. The third dose was not given. SL-325 Was Safe

and Well Tolerated Across a Wide Dosing Range Data are inclusive of all participants in all SAD and MAD cohorts TEAE observed in ≥2 participants included: headache, nasal congestion, nausea, venipuncture site pain, cough, diarrhea,

feeling hot, hyperhidrosis, dizziness, urinary tract infection, arthropod bite, and elective termination of pregnancy Mild TRAE (all Grade 1) observed in ≥2 participants included: headache (n=8), hyperhidrosis (n=2), dizziness

(n=2), feeling hot (n=2) SL-325 was discontinued in one participant who experienced a mild IRR (Grade 1)* SL-325 DOSE LEVEL (mg/kg) Placebo 0.1 0.3 1.0 3.0 10 30 N 18 6 6 12 12 12 6 ≥ 1 TEAE 5 2 2 6 7 4 2 ≥ 1 TRAE Mild (SAD) 1 0 0 1 2 0

1 Mild (MAD) 0 - - 2 3 3 - Moderate 0 0 0 0 0 0 0 Severe 0 0 0 0 0 0 0 Serious AE 0 0 0 0 0 0 0 Discontinued Due to TRAE 0 0 0 0 0 1* 0

*Cytokine panel evaluated:

IFNγ, TNFα, IL-1β, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12 and IL-13 No Evidence of Residual DR3 Agonism in Phase 1 in Healthy Human Participants The risk of agonism must be discharged for receptor targeted antibodies No SL-325 mediated

changes in serum cytokines were observed (IFNγ shown as example below)* No change from baseline in the serum concentration of TL1A was observed These data corroborate our preclinical findings that SL-325 is a pure DR3 blocking antibody Dose

Level No changes from pre-dose in proportions of cells (upper panels), nor the proportion of proliferating cells (lower panels) at any dose level

PK Profile of SL-325 from Phase 1

in Healthy Human Participants Dose proportional increase in Cmax and AUClast across all dose levels from 0.1 to 30 mg/kg Clearance consistent across all dose levels Estimated half-life of 16 days Figure shows participant-level PK profiles from all

SAD cohorts Accumulation ratio of between 1.64-1.75 with repeated dosing

A Single Dose of SL-325 Blocked

TL1A Binding in a Dose-Dependent Manner for Months DR3 occupancy was measured by inhibition of TL1A binding Full DR3 occupancy was achieved even at the lowest dose of 0.1 mg/kg Dose-dependent extension in the duration of TL1A blockade was observed,

lasting months at ≥1 mg/kg Durable inhibition of TL1A binding could enable quarterly dosing intervals in the maintenance phase of therapy for SL-325 Shattuck has developed a subcutaneous formulation of SL-325, and these data also potentially

indicate feasibility of administration with an autoinjector pen

*Wang Y et al. Pharm Res

2012;29:3384-3392, Wang Y ASCPT 2017 Anti-Drug Antibody (ADA) Assay Performance and Data Interpretability Inadequate assay tolerance contributes to a commonly held belief that higher doses of drug lead to lower incidence of ADA Sponsors

commonly report ADA qualitatively, or simply report an ADA percentage ADA assay results are only valid if the serum concentration of the therapeutic antibody is below the assay’s drug tolerance threshold (Assay Tolerance) at the time of sample

analysis FDA has reported that only 25% of antibodies have sufficient drug tolerance in the ADA assay at the time of BLA submission* This may be a source of high rates of false-negative results in reported ADA percentages, especially in

high-dose cohorts.

*ADA rates are provided as they

were reported in the referenced publications/reports. These data were not generated in head-to-head clinical trials. Comparisons across trials have inherent limitations and caution should be exercised when comparing data from unrelated

studies. **Data as of June 8, 2026. As of the cutoff date, ADA follow up complete for all SAD cohorts and the 1.0 mg/kg MAD cohort. For the 3.0 mg/kg and 10 mg/kg MAD cohorts, each participant has had at least three valid negative ADA assay results,

including after the last dose, with continued confirmatory follow-up ongoing. SL-325 Demonstrated a Potentially Best-In-Mechanism Immunogenicity Profile with 3.7% ADA SL-325 ADA assay has a sensitivity of 5 ng/mL and assay tolerance up to SL-325

concentrations of 160 µg/mL in serum Data includes all participants from all SAD and MAD cohorts in all dose levels in the study** ADA were observed in 2/54 participants who received SL-325. In the two participants who developed ADA,

titers remained low (8 and 16), without any impact on PK or RO Longitudinal sampling was performed to ensure that SL-325 concentrations fell within the dynamic range of the ADA assay for all study participants Reported ADA Rates from Phase 1

Trials* Afimkibart ADA titer of ≤60 was reported as ADA negative: Danese S et al. Lancet Gastroenterol and Hepatol. 2025;10:882-895 SL-325 ADA rate is 0% when analyzed using this cutoff.

Key Questions Answered in Phase 1

for SL-325 Is SL-325 as well-tolerated as anti-TL1A antibodies? Yes, SL-325 was well tolerated across a wide dosing range. Does human data confirm that SL-325 is a pure DR3 blocking antibody? Yes, SL-325 is a pure blocking antibody with no evidence

of residual agonism. How durable is DR3 occupancy, and what does that translate to for expected maintenance dosing intervals? A single dose of SL-325 inhibits TL1A binding to DR3 for months, potentially enabling quarterly dosing intervals. Is SL-325

less immunogenic than TL1A blocking antibodies? Potentially best-in-mechanism immunogenicity profile with ADA rate of 3.7%

*Study design as currently

contemplated, subject to change Study Design Elements Double-blind, placebo-controlled IV induction and maintenance Dose selection informed by Phase 1 PK/RO based QSP modeling with >95% TL1A signal inhibition throughout the dosing interval

Population Moderate to severe CD (CDAI 220-450) All patients have opportunity to receive SL-325 N = 174, randomized 1:1:1 Key Endpoints Primary: Endoscopic response at 12 weeks Secondary: Clinical remission at 12 weeks HD = high dose, LD = low dose,

LTE = long term extension SL-325 HD Placebo SL-325 HD SL-325 HD Blinded SL-325 LD SL-325 LD 12 Week Induction 40 Week Maintenance à LTE A Multi-Dose, Placebo-Controlled Planned Phase 2b Study of SL-325 in Crohn’s Disease

SL-846 A Potentially First-in-Class

DR3 x IL-23R Bispecific Antibody

Strategies to Block TL1A/DR3 in

Future Combination Therapy Created in https://BioRender.com

TL1A-Directed Bispecific Antibodies

Are Hyper-Immunogenic Kroenke M et al. Frontiers Immunol 2021; Neelakantan S et al. Br J Clin Pharmacol 2026 Genovese M et al. Arth & Rheumatol 2018; Kroenke M et al. AAPS Journal 2021 Created in https://BioRender.com

SL-846 – A Potentially

First-In-Class DR3 x IL-23R Half-Life Extended Bispecific Antibody DR3 Binding Arm IL-23R Binding Arm Same binding epitope as SL-325 Avoids risk of immune complex formation Enables binding in cis to IL-23R expressing cells Validated mechanism of

action (icotrokinra) Similar in vitro potency when compared to icotrokinra and risankizumab Enables binding in cis to DR3 expressing cells Effector-Null Human IgG1 Fc Mutations to remove Fc gamma receptor binding potential Knob-In-Hole Recombination

Clinically validated bispecific antibody format Half-Life Extended Substitutions to increase exposure and allow for extended dosing intervals

*Sequence equivalents of

tulisokibart, risankizumab, and icotrokinra SL-846 Demonstrated Competitive In Vitro Potency to Icotrokinra and Risankizumab SL-846 was tested head-to-head against tulisokibart, risankizumab and icotrokinra* in a variety of in vitro binding and

potency assays SL-846 performed similarly to, or slightly better than, each assay relative to the TL1A or IL-23 control Additional pre-clinical characterization of SL-846 versus controls will be provided at an upcoming medical meeting

Conclusions SL-325 Has the Profile

of a Winning Antibody Phase 2 Initiation in CD Expected in Q3 2026 12W Induction Data Expected in 1H 2028 SL-846 is a Potentially First-In-Class DR3 x IL-23R Bispecific Antibody NHP Tox/Immunogenicity Data Expected in 2H 2026 Phase 1 Initiation

Expected in 1H 2027 Potentially best-in-mechanism ADA rate from the completed Phase 1 study with a highly drug-tolerant assay and longitudinal sampling SL-325 was well-tolerated across a wide dose range, with a safety profile consistent with those

reported for the TL1A class PK and RO results support the potential for extended dosing intervals during maintenance therapy while maintaining full blockade of TL1A binding Low dose levels required for durable RO potentially indicate feasibility of

administration with a SC autoinjector pen SL-325 will soon enter a Phase 2b clinical proof of concept study in Crohn’s Disease Unlocks blockade of the TL1A/DR3 pathway in a bispecific without immune complex related ADA risk associated with

TL1A antibodies Pre-clinical studies showed similar potency to icotrokinra and risankizumab Leverages the clinical data generated to date with SL-325 Combination in a single drug enables simpler clinical proof of concept study designs with two of

the most promising target classes in I&I disease Opens portfolio expansion to target indications where IL-23 inhibition is clinically validated

Thank You SHATTUCK LABS, INC.

NASDAQ: STTK INVESTORRELATIONS@SHATTUCKLABS.COM

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Local phone number for entity.

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No definition available.

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Boolean flag that is true when the Form 8-K filing is intended to satisfy the filing obligation of the registrant as pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

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Boolean flag that is true when the Form 8-K filing is intended to satisfy the filing obligation of the registrant as pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act.

+ References

Reference 1: http://www.xbrl.org/2003/role/presentationRef

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- Definition

Title of a 12(b) registered security.

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Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

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-Section 12

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- Definition

Name of the Exchange on which a security is registered.

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Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Exchange Act

-Number 240

-Section 12

-Subsection d1-1

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Boolean flag that is true when the Form 8-K filing is intended to satisfy the filing obligation of the registrant as soliciting material pursuant to Rule 14a-12 under the Exchange Act.

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Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

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Trading symbol of an instrument as listed on an exchange.

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No definition available.

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Boolean flag that is true when the Form 8-K filing is intended to satisfy the filing obligation of the registrant as written communications pursuant to Rule 425 under the Securities Act.

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Reference 1: http://www.xbrl.org/2003/role/presentationRef

-Publisher SEC

-Name Securities Act

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