ADI-001 clinical development program now
addresses six autoimmune diseases
Patient enrollment for idiopathic inflammatory
myopathy and stiff person syndrome cohort expected to be initiated
in the first quarter of 2025
Company plans to report initial clinical data
from Phase 1 study in multiple autoimmune diseases in the first
half of 2025
Adicet Bio, Inc. (Nasdaq: ACET), a clinical stage biotechnology
company discovering and developing allogeneic gamma delta T cell
therapies for autoimmune diseases and cancer, today announced that
the U.S. Food and Drug Administration (FDA) has agreed to an
amendment to the Company’s Investigational New Drug (IND)
application to evaluate ADI-001 in idiopathic inflammatory myopathy
(IIM) and stiff person syndrome (SPS) as part of the ongoing Phase
1 trial in autoimmune diseases. The Company plans to initiate
enrollment for IIM and SPS patients in the first quarter of 2025.
This announcement follows the FDA’s recent agreements on amendments
to the Company’s ADI-001 IND application to evaluate three
additional indications beyond lupus nephritis (LN), including
systemic lupus erythematosus (SLE), systemic sclerosis (SSc) and
anti-neutrophil cytoplasmic autoantibody (ANCA)-associated
vasculitis (AAV).
“The FDA’s acceptance of our IND amendment to evaluate ADI-001
in patients with IIM and SPS builds on our recent momentum in
autoimmune diseases, expanding our efforts to six autoimmune
indications as we aim to bring our differentiated gamma delta T
cell therapy candidates to more patients in need of new treatment
options,” said Chen Schor, President and Chief Executive Officer at
Adicet Bio. “Following our recent announcement highlighting
clinical biomarker data which demonstrated robust B-cell depletion
and preferential trafficking to tissues and organs, we believe in
ADI-001’s best-in-class potential for the treatment of autoimmune
diseases, and we look forward to initiating patient enrollment in
IIM and SPS in the first quarter of 2025 in our ongoing Phase 1
clinical program.”
The ADI-001 Phase 1 program in autoimmune diseases will have
four separate arms, enrolling LN and SLE patients into one arm, SSc
patients into a second arm, AAV patients into a third arm, and IIM
and SPS patients into a fourth arm. The fourth cohort combines
several rare autoimmune muscle diseases into a single dose-finding
population, including SPS and the following IIM subtypes:
dermatomyositis, anti-synthetase syndrome, immune-mediated
necrotizing myopathy, polymyositis, and overlap myositis. Enrolled
patients will receive a single dose of ADI-001. The dose-limiting
toxicity window is 28 days with response and safety assessments
conducted on Day 28 and during the follow up period on months 3, 6,
9, 12, 18, and 24. The primary objectives of the study are to
evaluate the safety and tolerability of ADI-001. Secondary
objectives include measuring cellular kinetics, pharmacodynamics,
changes in autoantibody titers, and appropriate disease activity
scores in each indication.
About Idiopathic Inflammatory Myopathy
Idiopathic inflammatory myopathy (IIM, or myositis) refers to a
group of rare autoimmune disorders characterized by chronic muscle
inflammation and progressive muscle weakness. IIM primarily affects
skeletal muscles but can also involve other organs such as the
lungs, heart, and skin. Five of the main subtypes include
dermatomyositis, anti-synthetase syndrome, immune-mediated
necrotizing myopathy, polymyositis, and overlap myositis, all of
which can lead to significant functional impairment and have the
potential to be life threatening. There is no available cure for
IIM and many patients on current treatments have refractory disease
and may experience significant side effects.
About Stiff Person Syndrome
Stiff person syndrome (SPS) is a rare neurological autoimmune
disorder characterized by severe muscle stiffness and spasms,
primarily affecting the torso and limbs. Muscle stiffness caused by
SPS often impairs mobility, making it difficult for patients to
walk, bend, or perform daily activities. Muscle spasms can be
triggered by sudden stimuli such as loud noises, physical contact,
or emotional distress, and can result in a "statue-like" posture
when severe. Due to its rarity and overlapping symptoms with other
conditions, SPS is frequently misdiagnosed, often as an anxiety
disorder or movement disorder. There is currently no available cure
for SPS.
About ADI-001
ADI-001 is an investigational allogeneic gamma delta chimeric
antigen receptor (CAR) T cell therapy targeting CD20 for the
treatment of autoimmune diseases. ADI-001 was granted Fast Track
Designation by the FDA for the treatment of relapsed/refractory
class III or class IV lupus nephritis (LN), and the ongoing Phase 1
study is also evaluating ADI-001 for the treatment of systemic
lupus erythematosus (SLE), systemic sclerosis (SSc),
anti-neutrophil cytoplasmic autoantibody (ANCA)-associated
vasculitis (AAV), idiopathic inflammatory myopathy (IIM, or
myositis), and stiff person syndrome (SPS). In the Phase 1 GLEAN
trial, ADI-001 was shown to target B-cells via an anti-CD20 CAR and
demonstrated robust exposure and complete CD19+ B-cell depletion
both in peripheral blood and secondary lymphoid tissue.
About Adicet Bio, Inc.
Adicet Bio, Inc. is a clinical stage biotechnology company
discovering and developing allogeneic gamma delta T cell therapies
for autoimmune diseases and cancer. Adicet is advancing a pipeline
of “off-the-shelf” gamma delta T cells, engineered with chimeric
antigen receptors (CARs), to facilitate durable activity in
patients. For more information, please visit our website at
https://www.adicetbio.com.
Forward-Looking Statements
This press release contains “forward-looking statements” of
Adicet within the meaning of the Private Securities Litigation
Reform Act of 1995 relating to the business and operations of
Adicet. The words “anticipate,” “believe,” “continue,” “could,”
“estimate,” “expect,” “intend,” “may,” “plan,” “potential,”
“predict,” “project,” “should,” “target,” “would” and similar
expressions are intended to identify forward-looking statements,
although not all forward-looking statements contain these
identifying words. These forward-looking statements include, but
are not limited to, express or implied statements regarding:
clinical development of Adicet’s product candidates, including
future plans or expectations for ADI-001 and the potential safety,
tolerability and efficacy of ADI-001 for the treatment of
autoimmune diseases; the potential for ADI-001 to be a
best-in-class treatment for autoimmune diseases; the clinical
development of ADI-001 in LN, SLE, SSc and AAV; and the expected
progress, timing and success of the Phase 1 clinical study of
ADI-001 in IIM and SPS, including timing and expectations for
enrollment and future data releases.
Any forward-looking statements in this press release are based
on management’s current expectations and beliefs of future events,
and are subject to a number of risks and uncertainties that could
cause actual results to differ materially and adversely from those
set forth in or implied by such forward-looking statements,
including without limitation, the effect of global economic
conditions and public health emergencies on Adicet’s business and
financial results, including with respect to disruptions to our
preclinical and clinical studies, business operations, employee
hiring and retention, and ability to raise additional capital;
Adicet’s ability to execute on its strategy including obtaining the
requisite regulatory approvals on the expected timeline, if at all;
that positive results, including interim results, from a
preclinical or clinical study may not necessarily be predictive of
the results of future or ongoing studies; clinical studies may fail
to demonstrate adequate safety and efficacy of Adicet’s product
candidates, which would prevent, delay, or limit the scope of
regulatory approval and commercialization; and regulatory approval
processes of the U.S. Food and Drug Administration and comparable
foreign regulatory authorities are lengthy, time-consuming, and
inherently unpredictable; and Adicet’s ability to meet production
and product release expectations. For a discussion of these and
other risks and uncertainties, and other important factors, any of
which could cause Adicet’s actual results to differ from those
contained in the forward-looking statements, see the section
entitled “Risk Factors” in Adicet’s most recent annual report on
Form 10-Q and subsequent filings with the U.S. Securities and
Exchange Commission (SEC), as well as discussions of potential
risks, uncertainties, and other important factors in Adicet’s other
filings with the SEC. All information in this press release is as
of the date of the release, and Adicet undertakes no duty to update
this information unless required by law.
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version on businesswire.com: https://www.businesswire.com/news/home/20241016854445/en/
Adicet Bio, Inc. Investor and Media Contacts
Investors: Anne Bowdidge abowdidge@adicetbio.com
Janhavi Mohite Precision AQ 212-362-1200
janhavi.mohite@precisionaq.com
Media: Kerry Beth Daly kbdaly@adicetbio.com
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