Shattuck Labs Announces Orphan Drug Designation Granted by the U.S. Food and Drug Administration (FDA) for SL-172154 for the Treatment of Acute Myeloid Leukemia (AML)
10 Juni 2024 - 1:30PM
Shattuck Labs, Inc. (Shattuck) (Nasdaq: STTK), a clinical-stage
biotechnology company pioneering the development of bifunctional
fusion proteins as a new class of biologic medicine for the
treatment of patients with cancer and autoimmune disease, today
announced that the U.S. FDA has granted orphan drug designation
(ODD) to lead clinical candidate SL-172154 for the treatment of
AML.
“AML patients have few options for treatment and a poor
prognosis. FDA’s decision to grant orphan drug designation to
SL-172154 highlights the urgent need for new treatment options,”
said Taylor Schreiber, M.D., Ph.D., Chief Executive Officer of
Shattuck. “This is an important first step in our progression to
later-stage clinical studies, and we look forward to presenting
additional data from the Phase 1B dose expansion clinical trial of
SL-172154 with azacitidine in frontline higher-risk myelodysplastic
syndromes and TP53m AML patients during a poster presentation at
the European Hematology Association 2024 Congress.”
The FDA’s Office of Orphan Products Development grants orphan
status to drugs being developed to treat, diagnose, or prevent a
rare disease or condition affecting fewer than 200,000 people in
the United States. Orphan Drug Designation is designed to provide
drug developers with various benefits to support the development of
novel drugs, including the potential for market exclusivity for
seven years upon FDA approval, eligibility for tax credits for
qualified clinical trials, and waiver of application fees.
About AML AML is a hematologic malignancy that
develops from clonal expansion of myeloid precursors residing in
the bone marrow. In patients with AML, leukemic blasts infiltrate
the bone marrow and disrupt normal hematopoiesis. According to the
National Cancer Institutes’ Surveillance, Epidemiology, and End
Results Program, in 2023, there were approximately 20,380 new cases
of AML in the U.S., with 11,310 deaths attributed to the disease.
The median age of diagnosis is 68 years with approximately
one-third of patients being diagnosed over the age of 75. More than
70% of patients 65 years or older will die from their disease
within one year of diagnosis. As of 2019, the five-year
relative survival rate for acute myeloid leukemia was approximately
32%.
About SL-172154SL-172154 (SIRPα-Fc-CD40L) is an
investigational ARC® fusion protein designed to simultaneously
inhibit the CD47/SIRPα checkpoint interaction and activate the CD40
costimulatory receptor to bolster an anti-tumor immune response in
patients with advanced cancer. Multiple Phase 1 clinical trials are
ongoing for patients with platinum-resistant ovarian cancer
(NCT04406623, NCT05483933) and patients with AML and HR-MDS
(NCT05275439).
About Shattuck Labs, Inc.Shattuck Labs, Inc.
(Nasdaq: STTK) is a clinical-stage biotechnology company pioneering
the development of bi-functional fusion proteins as a new class of
biologic medicine for the treatment of patients with cancer and
autoimmune disease. Compounds derived from Shattuck’s proprietary
Agonist Redirected Checkpoint (ARC®) platform are designed to
simultaneously inhibit checkpoint molecules and activate
costimulatory molecules with a single therapeutic. The company’s
lead SL-172154 (SIRPα-Fc-CD40L) program, which is designed to block
the CD47 immune checkpoint and simultaneously agonize the CD40
pathway, is being evaluated in multiple Phase 1 trials. Shattuck
has offices in both Austin, Texas and Durham, North Carolina. For
more information, please visit: www.ShattuckLabs.com.
Forward-Looking StatementsCertain statements in
this press release may constitute “forward-looking statements”
within the meaning of the federal securities laws, including, but
not limited to, statements regarding: future presentations of
clinical data; clinical development plans and strategies for
SL-172154; timing of anticipated clinical data; future plans for
Shattuck’s pipeline; and Shattuck’s strategies. Words such as
“anticipate,” “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 the company 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 the company’s control and subject
to change. Actual results could be materially different. Risks and
uncertainties which could cause such outcomes to change include:
global macroeconomic conditions and related volatility;
expectations regarding the initiation, progress, and expected
results of Shattuck’s preclinical studies, clinical trials and
research and development programs; expectations regarding the
timing, completion and outcome of the company’s 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 and other
risks and uncertainties identified in Shattuck’s Annual Report on
Form 10-K for the year ended December 31, 2023 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.
Shattuck 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: Conor
RichardsonVice President of Investor RelationsShattuck Labs,
Inc.InvestorRelations@shattucklabs.com
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