Data presented at the 2022 Annual Meeting of
the American Association of Cancer Research
- New data from an open-label preclinical study in mice
evaluating the changes in immune-related genes induced by multiple
combinations of NBTXR3, anti-PD-1, anti-LAG-3, and anti-TIGIT
showed that groups that received NBTXR3 along with checkpoint
inhibitors outperformed all other combinations in efficacy,
survival, and induction of long-term anti-cancer memory
- This new analysis concluded that NBTXR3 plus a triple
blockade of PD-1, LAG-3, and TIGIT (Combination therapy) promotes
immune activation at the irradiated site, abscopal responses at
non-irradiated sites, and suggests that the Combination therapy may
be effective against metastatic cancers
Regulatory News:
NANOBOTIX (Euronext : NANO –– NASDAQ: NBTX – the
‘‘Company’’), a clinical-stage biotechnology company
pioneering physics-based approaches to expand treatment
possibilities for patients with cancer, today announced new data
from an open-label preclinical study evaluating the combination of
first-in-class radioenhancer, NBTXR3, with the triple blockade of
PD-1, LAG-3, and TIGIT (“Combination therapy”). The data were
published via E-Poster presentation at the 2022 Annual Meeting of
the American Association of Cancer Research (AACR), held April
8-13, 2022, by researchers from The University of Texas MD Anderson
Cancer Center (MD Anderson).
“We believe that the potential immune priming effect of
radiotherapy-activated NBTXR3 could prove to be a game-changer for
cancer immunotherapy,” said Laurent Levy, co-founder and chairman
of the executive board at Nanobiotix. “Our view is that while new
immunotherapy treatment modalities with the potential to improve
outcomes for patients continue to emerge, they remain reliant upon
an underlying immune response. This new preclinical gene expression
data showing that the addition of NBTXR3 enhanced activity in key
immune pathways associated with innate and adaptive immunity, and
outperformed all other combinations in efficacy, survival, and
induction of long-term anti-cancer memory, adds to a growing body
of support for NBTXR3 as a product candidate that could potentially
help expand the benefits of immunotherapy to larger share of the
patients we serve.”
PRECLINICAL DATA ON IMMUNOTHERAPY BLOCKADE PLUS
RADIOTHERAPY-ACTIVATED NBTXR3
Previously reported preclinical and clinical data evaluating
NBTXR3 in combination with diverse immune checkpoint inhibitors
(ICIs) including anti-PD-1, anti-CTLA-4, anti-LAG-3, and anti-TIGIT
suggest that, after activation by radiotherapy, the radioenhancer
may induce an “immune priming” effect that could help improve and
expand the benefits of ICIs to more patients.
This new analysis, presented at AACR, assessed immune gene
expression associated with multiple combinations of NBTXR3,
anti-PD-1, anti-LAG-3, and anti-TIGIT.
Key Findings Include:
- The Combination therapy outperformed all other tested treatment
regimens in efficacy, survival, and induction of long-term
anti-cancer memory
- The Combination therapy significantly promoted the upregulation
of mRNA transcripts involved in innate immunity, the humoral
response, B cell function, dendritic cell function, and antigen
processing within primary, irradiated tumors relative to untreated
controls
- Within non-irradiated tumors, the Combination therapy produced
elevations in multiple immune-related pathways that were
significantly higher than those produced by other treatment
combinations and these pathways included both adaptive and innate
immunity; B, T, natural killer, and dendritic cell function; and
antigen processing
- The Combination therapy promoted immune activation at the
irradiated site, abscopal immune responses are improved with the
addition of LAG-3 and TIGIT to PD-1 and radiotherapy-activated
NBTXR3, and the data suggest that the Combination therapy may be
effective against metastatic cancers
***
About NBTXR3 NBTXR3 is a novel, potentially
first-in-class oncology product, composed of functionalized hafnium
oxide nanoparticles that is administered via one-time intratumoral
injection and activated by radiotherapy. The product candidate’s
physics-based mechanism of action (MoA) is designed to induce
significant tumor cell death in the injected tumor when activated
by radiotherapy, subsequently triggering adaptive immune response
and long-term anti-cancer memory. Given the MoA, Nanobiotix
believes that NBTXR3 could be scalable across any solid tumor that
can be treated with radiotherapy and across any therapeutic
combination, particularly, with immune checkpoint inhibitors.
NBTXR3 is being evaluated in locally advanced head and neck
squamous cell carcinoma (HNSCC) as the primary development pathway.
The company-sponsored phase I dose escalation and dose expansion
study has produced favorable safety data and early signs of
efficacy. In February 2020, the United States Food and Drug
Administration granted regulatory Fast Track designation for the
investigation of NBTXR3 activated by radiation therapy, with or
without cetuximab, for the treatment of patients with locally
advanced HNSCC who are not eligible for platinum-based
chemotherapy.
Nanobiotix has also prioritized an Immuno-Oncology development
program—beginning with a Company sponsored phase I clinical study,
evaluating NBTXR3 activated by radiotherapy in combination with
anti-PD-1 checkpoint inhibitors for patients with locoregional
recurrent or recurrent/metastatic HNSCC and for patients with lung
or liver metastases from any primary cancer eligible for anti-PD-1
therapy, either naïve or resistant to prior PD-1 (either primary or
secondary as per SITC criteria).
Given the Company’s focus areas, and balanced against the
scalable potential of NBTXR3, Nanobiotix has engaged in strategic
collaborations to expand development of the product candidate in
parallel with its priority development pathways. Pursuant to this
strategy, in 2019 Nanobiotix entered into a broad, comprehensive
clinical research collaboration with The University of Texas MD
Anderson Cancer Center to sponsor several phase I and phase II
studies to evaluate NBTXR3 across tumor types and therapeutic
combinations. In 2021, the Company entered into an additional
strategic collaboration agreement with LianBio to support its
global phase III study in Asia along with four future
registrational studies.
About NANOBIOTIX Nanobiotix is a late-stage clinical
biotechnology company pioneering disruptive, physics-based
therapeutic approaches to revolutionize treatment outcomes for
millions of patients; supported by people committed to making a
difference for humanity. The company’s philosophy is rooted in the
concept of pushing past the boundaries of what is known to expand
possibilities for human life.
Incorporated in 2003, Nanobiotix is headquartered in Paris,
France. The company also has subsidiaries in Cambridge,
Massachusetts (United States), France, Spain, Germany and
Switzerland.
Nanobiotix has been listed on the regulated market of Euronext
in Paris since 2012 and on the Nasdaq Global Select Market in New
York City since December 2020.
Nanobiotix is the owner of more than 30 umbrella patents
associated with three (3) nanotechnology platforms with
applications in 1) oncology; 2) bioavailability and
biodistribution; and 3) disorders of the central nervous system.
The company's resources are primarily devoted to the development of
its lead product candidate– NBTXR3 —which is the product of its
proprietary oncology platform and has already achieved market
authorization in Europe for the treatment of patients with soft
tissue sarcoma under the brand name Hensify®.
For more information about Nanobiotix, visit us at
www.nanobiotix.com or follow us on LinkedIn and Twitter.
Disclaimer This press release contains certain
“forward-looking” statements within the meaning of applicable
securities laws, including the Private Securities Litigation Reform
Act of 1995. Forward-looking statements may be identified by words
such as “at this time,” “anticipate,” “believe,” “expect,”
“intend,” “on track,” “plan,” “scheduled,” and “will,” or the
negative of these and similar expressions. These forward-looking
statements, which are based on our management’s current
expectations and assumptions and on information currently available
to management, include statements about the timing and progress of
clinical trials, the timing of our presentation of data, the
results of our preclinical and clinical studies and their potential
implications. Such forward-looking statements are made in light of
information currently available to us and based on assumptions that
Nanobiotix considers to be reasonable. However, these
forward-looking statements are subject to numerous risks and
uncertainties, including with respect to the risk that subsequent
studies and ongoing or future clinical trials may not generate
favorable data notwithstanding positive early clinical results and
the risks associated with the evolving nature of the duration and
severity of the COVID-19 pandemic and governmental and regulatory
measures implemented in response to it. Furthermore, many other
important factors, including those described in our Annual Report
on Form 20-F filed with the U.S. Securities and Exchange Commission
(the SEC) on April 8, 2022 under “Item 3.D. Risk Factors” and those
set forth in the universal registration document of Nanobiotix
filed with the French Financial Markets Authority (Autorité des
Marchés Financiers – the AMF) on April 8, 2022, each as updated in
our Half-Year Financial Report filed with the AMF and the SEC on
September 8, 2021 (a copy of which is available on
www.nanobiotix.com), as well as other known and unknown risks and
uncertainties may adversely affect such forward-looking statements
and cause our actual results, performance or achievements to be
materially different from those expressed or implied by the
forward-looking statements. Except as required by law, we assume no
obligation to update these forward-looking statements publicly, or
to update the reasons why actual results could differ materially
from those anticipated in the forward-looking statements, even if
new information becomes available in the future.
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version on businesswire.com: https://www.businesswire.com/news/home/20220411005791/en/
Nanobiotix Communications Department Brandon Owens VP,
Communications +1 (617) 852-4835 contact@nanobiotix.com
Investor Relations Department Kate McNeil SVP, Investor
Relations +1 (609) 678-7388 investors@nanobiotix.com
Media Relations FR – Ulysse Communication Pierre-Louis
Germain +33 (0) 6 64 79 97 51
plgermain@ulysse-communication.com
US – Porter Novelli Caitlin Hunt +1 (781) 985-5967
Caitlin.Hunt@porternovelli.com
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