PolTREG receives US Patent Office Notice of Allowance for Treg cell therapy to treat Type-1 Diabetes
16 Janeiro 2024 - 3:00AM
Gdańsk, Poland – 16 January 2024, 07:00 CET –
PolTREG S.A. (Warsaw Stock Exchange: PTG), a clinical-stage
biotechnology company in Europe developing cell therapies for use
in a wide range of autoimmune diseases, announced it received a
Notice of Allowance from the United States Patent and Trademark
Office (USPTO), covering the manufacturing of T-regulatory cells
(T-reg) to treat Type-1 Diabetes (T1D), and ways the therapy is
administered. The US allowance constitutes an important addition to
the intellectual property portfolio covering PolTREG’s autoimmune
therapies.
“This USPTO decision complements our extensive intellectual
property portfolio in the US and EU, paving the way for rapid,
unimpeded commercialization of PolTREG’s cell therapies,” said
PolTREG CEO Prof Piotr Trzonkowski. “Together with
our 17 years of experience with patients at our own facilities in
Poland, our dominant intellectual property portfolio demonstrates
that we are leading pioneers in the field of T-reg therapeutics for
autoimmune disorders. Indeed, we are the first ever to have
administered Treg cell therapies to patients and the first company
to begin receiving revenues from sales of our lead product; so far,
27 patients have been successfully treated commercially under the
Hospital Exemption program in Poland.”
The US patent application covers the manufacturing of Treg
cells, the formula of the cellular medicinal product containing
Treg cells, and the ways the therapy is administered in T1D
patients.
Many of PolTREG’s patent submissions are primary in the field,
given that its team performed the first-in-human trials with Treg
cell therapies in graft-versus-host disease in 2007-2009. PolTREG’s
portfolio of patents and patent applications, in U.S. and Europe,
includes the formulation of polyclonal and engineered Treg
products, unique manufacturing elements of these cell therapies,
details of patient recruitment and clinical efficacy. A number of
the patents have been licensed from the Medical University of
Gdańsk to PolTREG through Prof Trzonkowski, who was responsible at
the university for the research behind these patents.
PolTREG boasts the most advanced pipeline for Treg cell
therapies in autoimmune disease, with its flagship drug candidate,
PTG-007, in clinical studies for two indications in T1D and two in
Multiple Sclerosis (MS).
Upcoming milestones in 2024
H1 2024 |
Results of a
long-term efficacy and safety study of PTG-007, in which the
company followed early-onset T1D patients over a period of 10
years |
H2 2024 |
Initiate Phase 2
clinical trial of PTG-007 in presymptomatic T1D patientsInitiate
Phase 1/2a trial in relapsing-remitting (RRMS) patientsInitiate
Phase 1/2a trial in primary progressive (PPMS) patientsPreclinical
proof-of-concept for product(s) from engineered Treg pipeline |
T-regulatory cells (Treg) are the regulators of
the immune system, seeing to it that other leukocytes do not attack
the body’s own cells. PolTREG has developed patented processes by
which it takes Treg from a patient’s own body, multiplies them ex
vivo, and then injects them back in the patient’s own bloodstream
for therapeutic effect. Treg therapeutics have advantages over
traditional drugs in that they only act at the site of the
inflammation, and switch off when the inflammation is over. A Phase
2 clinical study in T1D showed half of patients in clinical
remission 24 months into the study, demonstrating the strong
potential PolTREG’s cell therapies have to become powerful
disease-modifying treatments.PolTREG (Gdańsk,
Poland; WSA:PTG) is a global leader in developing autoimmune
therapies based on T-regulatory cells (Tregs). Its lead product,
PTG-007, autologous Treg treatment for early-onset Type-1 Diabetes
(T1D) is ready to start Phase 2/3 clinical testing, upon
partnership. The company will launch Phase 2 trials for PTG-007 to
treat Multiple Sclerosis (MS), in the second half of 2024 for RRMS
and PPMS. PolTREG also is developing engineered Tregs, including
CAR-Tregs, antigen-specific Tregs and TCR-Tregs, all of which are
in the preclinical stage. PolTREG has completed four clinical
trials with more than 100 patients treated with Tregs. For more
information please visit www.poltreg.com.
For further information please contact:
PolTREG
S.A.Prof Piotr TrzonkowskiChief Executive
Officerir@poltreg.com+48 512 532 401 |
Investor
RelationsChris MaggosCohesion Bureau+41 79 367 62
54chris.maggos@cohesionbureau.com Media Relations
Douwe MiedemaCohesion Bureaudouwe.miedema@cohesionbureau.com
|
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and include statements the Company makes concerning the intended
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cautioned that any such forward-looking statements are not
guarantees of future performance. The company's actual results may
differ materially from those predicted by the forward-looking
statements. The company undertakes no obligation to publicly update
or revise forward-looking statements, except as may be required by
law.
- 20240116 PolTREG press release US patent_final
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