Allakos Announces First Patient Dosed in Phase 1 Trial of AK006 in Chronic Spontaneous Urticaria
28 Maggio 2024 - 1:02PM
Allakos Inc. (Nasdaq: ALLK), a biotechnology company developing
AK006 for the treatment of mast cell-driven diseases, today
announced that the first patient with chronic spontaneous urticaria
(CSU) has been dosed in a randomized, double-blind,
placebo-controlled Phase 1 trial of AK006. The Phase 1 trial is
designed to assess the safety, tolerability and pharmacokinetics of
AK006, and to explore the therapeutic effects of AK006 in patients
with CSU using the urticaria activity score (UAS7) at 14 weeks.
Top-line results from the trial are expected at year end 2024.
Chronic Spontaneous Urticaria
CSU symptoms are caused by the inappropriate activation of mast
cells in the skin. IgE-dependent mast cell activation has been
identified as a pathogenic driver of CSU, and agents which target
this pathway have demonstrated therapeutic activity. More recently,
IgE-independent pathways, such activation through the MRGPRX2
receptor, have been implicated in CSU disease pathogenesis. Agents
that target both IgE-dependent and IgE-independent modes of mast
cell activation have the potential to work in a broader patient
population or show greater symptom improvement.
About AK006
AK006 is a humanized IgG1 monoclonal antibody which activates
the inhibitory receptor Siglec-6. Siglec-6 is found on the surface
of mature mast cells and offers a way to selectively target mast
cells. In preclinical experiments, AK006 inhibits IgE-dependent and
IgE-independent mast cell activation including activation through
IgE, MRGPRX2 and KIT receptors. In these experiments, AK006 drives
deep mast cell inhibition and, in addition to its inhibitory
activity, can reduce mast cell numbers via antibody-dependent
cellular phagocytosis in the presence of activated macrophages.
Phase 1 trial in Chronic Spontaneous
Urticaria
AK006 is being studied in a Phase 1 randomized, double-blind,
placebo-controlled single and multiple ascending dose trial that
includes a randomized, double-blind, placebo-controlled CSU arm
(NCT06072157). The CSU arm will enroll up to 60 adult patients with
antihistamine refractory CSU (including patients with prior
biologics treatment). Patients will be randomized 2:1 to receive
intravenous AK006 or placebo once every four weeks (Q4W). The
primary efficacy analysis will be the change in the urticaria
activity score (UAS7) at week 14. Data from approximately 30
patients is expected at year end 2024.
About Allakos
Allakos is a clinical stage biotechnology company developing
therapeutics that target immunomodulatory receptors present on
immune effector cells involved in allergy, inflammatory and
proliferative diseases. Activating these immunomodulatory receptors
allows for the direct targeting of cells involved in disease
pathogenesis and, in the setting of allergy and inflammation, has
the potential to result in broad inhibition of inflammatory cells.
The Company’s most advanced antibody in ongoing clinical
development is AK006. AK006 targets Siglec-6, an inhibitory
receptor expressed on mast cells. Mast cells are widely distributed
in the body and play a central role in the inflammatory response.
Inappropriately activated mast cells have been identified as key
drivers in a number of severe diseases affecting the
gastrointestinal tract, eyes, skin, lungs and other organs. In
preclinical studies, AK006 appears to provide deep mast cell
inhibition and, in addition to its inhibitory activity, reduce mast
cell numbers. For more information, please visit the Company’s
website at www.allakos.com.
Forward-Looking Statements
This press release contains forward-looking statements within
the meaning of the Private Securities Litigation Reform Act of 1995
as contained in Section 27A of the Securities Act of 1933, as
amended, and Section 21E of the Securities Exchange Act of 1934, as
amended. Such forward-looking statements include, but are not
limited to, Allakos’ progress, business plans, areas of focus and
preclinical research; enrollment in Allakos’s clinical study;
timing and availability of data; the potential of AK006; and
Allakos’ anticipated milestones. Such statements are subject to
numerous important factors, risks and uncertainties that may cause
actual events or results to differ materially from current
expectations and beliefs, including but not limited to: Allakos’
stages of clinical drug development; Allakos’ ability to timely
initiate and complete clinical trials for AK006; Allakos’ ability
to obtain required regulatory approvals for its clinical trials;
uncertainties related to the enrollment of patients in its clinical
trials; Allakos’ ability to demonstrate sufficient safety and
efficacy of its product candidates in its clinical trials;
uncertainties related to the success of clinical trials, regardless
of the outcomes of preclinical testing or early-stage trials;
Allakos’ ability to advance additional product candidates beyond
AK006; uncertainties related to Allakos’ ability to realize the
contemplated benefits of its restructuring and related reduction in
force; Allakos’ ability to accurately forecast financial results;
Allakos’ ability to obtain additional capital to finance its
operations, research and drug development; general economic and
market conditions, both domestic and international; domestic and
international regulatory obligations; and other risks. Information
regarding the foregoing and additional risks may be found in the
section entitled “Risk Factors” in documents that Allakos files
from time to time to with the SEC. These documents contain and
identify important factors that could cause the actual results for
Allakos to differ materially from those contained in Allakos’
forward-looking statements. Any forward-looking statements
contained in this press release speak only as of the date hereof,
and Allakos specifically disclaims any obligation to update any
forward-looking statement, except as required by law. These
forward-looking statements should not be relied upon as
representing Allakos’ views as of any date subsequent to the date
of this press release.
Source: Allakos Inc.
Investor Contact:Adam Tomasi, PresidentAlex Schwartz, VP
Strategic Finance and Investor Relationsir@allakos.com
Media Contact:Denise Powelldenise@redhousecomms.com
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