Corporate Overview
NASDAQ: STTK
January 10, 2021
Forward-Looking Statements
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, including statements concerning our plans, objectives, goals, strategies, future events, plans or intentions relating to products and markets, the safety, efficacy and clinical benefits of our product candidates, the anticipated timing of our planned clinical trials, including initiation of additional cohorts, the anticipated timing for data, the association of preclinical data with potential clinical benefit, the timing of anticipated milestones, plans and objectives of management for future operations and future results of anticipated product development efforts, the timing of expected announcements, and our liquidity and capital resources and business trends are all forward-looking statements. 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," 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 the effects from the COVID-19 pandemic on our clinical trial activities, the uncertainties inherent in the clinical drug development process, such as the regulatory approval process, the timing of our regulatory filings, the potential for substantial delays, and the risk that earlier study results may not be predictive of future study results, manufacturing risks, and competition from other therapies or products, 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, 2020 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.
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Shattuck Labs
Focused on Improving the Lives of Patients
OUR PURPOSE
Pioneering Novel Therapeutics for Cancer and Autoimmune Diseases
OUR VALUES
Bold, Respectful, Honest, Balanced, Grateful
OUR MISSION
Work with a sense of urgency, focused on scientific excellence and thoughtful stewardship of resources, to translate innovative ideas into medicines that improve the lives of patients with serious diseases
OUR VISION
Build incredible medicines off the beaten path by challenging ourselves to think differently
Shattuck Labs Overview
Shattuck Labs (NASDAQ: STTK)
Next-Generation
Fusion Protein
Platforms
Clinical-stage biotechnology company pioneering the development of bi-functional fusion proteins designed to fundamentally transform therapeutic immune modulation
• > 400 unique bi-functional fusion proteins | ||
• Checkpoint inhibition + Costimulatory pathway activation | ||
• | High binding affinity / avidity to targets | |
ARC Platform | • | Rapid Concept to Compound to Clinic |
GADLEN Platform |
Clinical Pipeline
Against Validated
Targets
SL-172154: CD47/SIRPα Inhibitor CD40 Agonist
Three Phase 1 trials in ovarian cancer,
HNSCC/CSCC, and AML/HR-MDS
SL-279252: PD-1/PD-L1 Inhibitor OX40 Agonist
Phase 1 trial in advanced solid tumors and lymphoma
Experienced
Team and Strong
Cash Position
- Highly experienced management team, board of directors, and scientific advisory board
- $290.2 million in cash and cash equivalents and marketable securities as of September 30, 2021
- Expected cash runway into 2H'2024 with multiple key clinical data readouts
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Highly Experienced Management, Board, and Advisors
Established Track Record of Drug Discovery and Development
Management Team
Board of Directors
Taylor Schreiber, MD, PhD
Chief Executive Officer
Lini Pandite, MD, MBA
Chief Medical Officer
Casi DeYoung, MBA
Chief Business Officer
Andrew R. Neill, MBA
Chief Financial Officer
Abhinav Shukla, PhD
Chief Technical Officer
Erin Ator Thomson, JD
General Counsel
George Fromm, PhD
VP of R&D
Suresh de Silva, PhD
VP of Product Development
Fatima Rangwala, MD, PhD
VP of Clinical Development
Tom Lampkin, PharmD
VP of Regulatory Affairs
James Stout, PhD
VP of Manufacturing
Kelli Collin, MS
VP of Quality
Bo Ma, PhD
VP of Biometrics
Sanjay Khandekar, PhD, MBA
VP of Strategic Marketing
Carrie Brownstein, MD | CMO of Cellectis; VP of Global Clinical R&D, Myeloid Diseases, Celgene |
Michael Lee | Redmile Group |
Neil Gibson, PhD | Chief Scientific Officer, COI Pharma; Chief Scientific Officer, Pfizer Oncology |
George Golumbeski, PhD | Chairman of the Board; EVP of Business Development, Celgene |
Helen M. Boudreau | CFO of Proteostasis, FORMA, Novartis US |
Tyler Brous | Portfolio Manager, Lennox Capital Partners, LP |
Taylor Schreiber MD, PhD | Chief Executive Officer, Shattuck |
Note: italicized text denotes prior affiliation |
Scientific Advisory Board
Johann De Bono, MD, PhD
Aurélien Marabelle, MD, PhD
Ignacio Melero, MD, PhD
Drew Pardoll, MD, PhD
Kurt Schalper, MD, PhD
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Shattuck Labs Inc. published this content on 10 January 2022 and is solely responsible for the information contained therein. Distributed by Public, unedited and unaltered, on 10 January 2022 19:37:07 UTC.