Allakos Announces Phase 1 Trial Results of Subcutaneous AK006 in Healthy Volunteers
October 10 2024 - 3:02PM
Allakos Inc. (Nasdaq: ALLK), a biotechnology company developing
AK006 for the treatment of mast cell-driven diseases, today
announced results from the Phase 1 study of subcutaneous AK006 in
healthy volunteers. AK006 is a Siglec-6 monoclonal antibody that
selectively inhibits mast cells. Inappropriate activation of mast
cells has been identified as a pathogenic driver of multiple
diseases, including chronic spontaneous urticaria, food allergy and
asthma.
Phase 1 Study Results of Subcutaneous AK006
in Healthy Volunteers
- Bioavailability of subcutaneous AK006 was approximately
77%.
- Subcutaneous administered AK006 showed an estimated half-life
of 12-22 days.
- Consistent with the IV formulation, skin biopsies taken from
subcutaneous AK006 treated healthy volunteers showed high levels of
receptor occupancy confirming AK006 reaches skin tissue mast cells.
- The 720 mg dose of AK006 showed 98% receptor occupancy at day
113 suggesting the potential for infrequent dosing.
- Single and multiple doses of IV AK006 and single dose
subcutaneous AK006 up to 720 mg were well-tolerated with a
favorable safety profile. In the safety profile to date:
- There were no serious adverse events (SAEs) in subjects on
AK006.
- There were no treatment emergent adverse events leading to
discontinuation of AK006.
- There were no dose limiting toxicities.
- The most common adverse events (≥10%) occurring more frequently
in subjects on AK006 were headache and dysmenorrhea, all of which
were mild-to-moderate in severity.
Phase 1 AK006 Study in Healthy Volunteers
and in Patients with Chronic Spontaneous Urticaria
AK006 is being studied in an ongoing Phase 1 single
ascending dose (SAD) and multiple ascending dose (MAD) trial that
includes a randomized, double-blind, placebo-controlled CSU arm
(NCT06072157). In June 2024 the company reported data from the SAD
and MAD IV cohorts of the study. The data announced today are from
the randomized, double-blind, placebo-controlled SAD subcutaneous
cohorts of the study. In these cohorts, healthy volunteers were
randomized 6:2 to receive doses of subcutaneous AK006 or placebo.
Two dosed levels, 150 mg and 720 mg, of subcutaneous AK006 were
tested. The primary objective was to evaluate the safety and
tolerability of single subcutaneous doses of AK006 in healthy
volunteers, establish the bioavailability and pharmacokinetics of
subcutaneous AK006, and to explore Siglec-6 receptor occupancy on
mast cells in skin biopsy samples.
In the CSU arm of the Phase 1 study, up to 60 adult
patients with antihistamine refractory CSU (including patients with
prior biologics treatment), will be randomized 2:1 to receive 720
mg of IV 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 in early Q1 of 2025.
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.
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 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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