Pandion Therapeutics Presents Preclinical Data Highlighting Potential of Tissue-Tethered PD-1 Agonist to Locally Target Autoi...
February 22 2021 - 8:30AM
Pandion Therapeutics, Inc. (Nasdaq: PAND), a clinical-stage
biotechnology company developing novel therapeutics designed to
address the unmet needs of patients living with autoimmune
diseases, today presented preclinical data on PT001, the Company’s
tissue-tethered PD-1 agonist, at the Network for Pancreatic Organ
Donors with Diabetes (nPOD) 13th Annual Scientific Meeting. The
research, done in collaboration with St Vincent’s Institute of
Medical Research in Australia and funded by JDRF and the JDRF T1D
Fund, showed that PT001 treatment delayed the onset of
hyperglycemia in a mouse model of Type 1 diabetes.
PD-1 plays a critical role in immune homeostasis
and its dysfunction is linked to the development of autoimmune
diseases, such as Type 1 diabetes, lupus and vitiligo. PD-1 is an
inhibitory receptor located on conventional T cells, which, when
activated, promotes the attenuation of an immune attack. PT001 is
designed to agonize, or activate, PD-1 receptors to reduce aberrant
immune responses in tissues expressing mucosal addressin cell
adhesion molecule (MAdCAM), such as the gastrointestinal tract,
liver, and inflamed pancreas.
“With tissue-tethered immunomodulation, we’re
able to increase locally the concentration of our therapeutic
candidates, driving robust responses in animal models that are not
possible with their untethered counterparts. We believe this opens
the door for Pandion to be at the forefront of addressing localized
autoimmune diseases in a new, more targeted way,” said Jo Viney,
Ph.D., President, Co-Founder and Chief Scientific Officer of
Pandion. “The data presented at nPOD give us confidence in pursuing
a tissue-tethered approach for T1D and other autoimmune diseases of
the pancreas in collaboration with JDRF and Astellas. We are in the
process of lead optimization for the PT001 program and expect to
nominate a development candidate in the first half of this
year.”
The Company plans to develop PT001 for
autoimmune diseases of the gut and liver, and potentially pancreas.
Pandion is also pursuing additional pancreas tethers as part of its
collaboration with Astellas to discover and develop novel compounds
for autoimmune diseases of the pancreas, including Type 1
diabetes.
The presentation, “A Novel PD-1:MAdCAM
Bifunctional Antibody for the Treatment of T1D,” was authored by D.
Rios, L. Edwards, S. Alioto, M. Proschitsky, R.
Taylor, S. Litwak, G. Jhala, H. Thomas, I.
Mascanfroni, N. Higginson-Scott, K. Kis-Toth, K. Otipoby,
and J Viney and is available on the Company’s website:
https://pandiontx.com/our-science/posters-presentations/.
About Pandion
TherapeuticsPandion Therapeutics is developing novel
therapeutics designed to address the unmet needs of patients living
with autoimmune diseases. Pandion’s TALON (Therapeutic Autoimmune
reguLatOry proteiN) drug design and discovery platform enables the
company to create a pipeline of product candidates using
immunomodulatory effector modules, with the ability to also combine
an effector module with a tissue-targeted tether module in a
bifunctional format. Pandion’s lead product candidate PT101, a
combination of an interleukin-2 mutein effector module fused to a
protein backbone, is designed to selectively expand regulatory T
cells systemically, without activating proinflammatory cells, such
as conventional T cells and natural killer cells. Pandion is
continuing to develop and expand its library of effector and tether
modules as part of its earlier-stage research and discovery
pipeline. For more information, please visit www.pandiontx.com
and engage with us on Twitter @PandionTX or on LinkedIn.
Forward-Looking StatementsThis
press release contains “forward-looking statements” within the
meaning of the Private Securities Litigation Reform Act of 1995
that involve substantial risks and uncertainties. All statements,
other than statements of historical facts, contained in this press
release, including statements regarding the Company’s strategy and
clinical development plans, timelines and prospects, are
forward-looking statements. The words “anticipate,” “believe,”
“continue,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,”
“potential,” “predict,” “project,” “should,” “target,” “will,”
“would” and similar expressions are intended to identify
forward-looking statements, although not all forward-looking
statements contain these identifying words. Any forward-looking
statements are based on management’s current expectations 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.
These risks and uncertainties include, but are not limited to,
risks associated with Pandion’s ability to obtain and maintain
necessary approvals from the FDA and other regulatory authorities;
initiate preclinical studies and clinical trials of PT101 and its
other product candidates; advance PT101 and its other product
candidates in preclinical research and clinical trials; replicate
in clinical trials positive results found in preclinical studies;
advance the development of its product candidates under the
timelines it anticipates in current and future clinical trials;
obtain, maintain or protect intellectual property rights related to
its product candidates; manage expenses; and raise the substantial
additional capital needed to achieve its business objectives. For a
discussion of other risks and uncertainties, and other important
factors, any of which could cause the Company’s actual results to
differ from those contained in the forward-looking statements, see
the “Risk Factors” section, as well as discussions of potential
risks, uncertainties and other important factors, in the Company’s
most recent filings with the Securities and Exchange Commission. In
addition, the forward-looking statements included in this press
release represent the Company’s views as of the date hereof and
should not be relied upon as representing the Company’s views as of
any date subsequent to the date hereof. The Company anticipates
that subsequent events and developments will cause the Company’s
views to change. However, while the Company may elect to update
these forward-looking statements at some point in the future, the
Company specifically disclaims any obligation to do so.
Contacts
Media:Kathryn MorrisThe Yates
Network914-204-6412kathryn@theyatesnetwork.com
Investors:Michelle AveryPandion
Therapeutics857-273-0444investors@pandiontx.com
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