Innate Pharma SA (Euronext Paris: IPH; Nasdaq: IPHA)
(“
Innate” or the “
Company”) today
announced that two oral presentations will be highlighted at the
ESMO 2021 Virtual Congress.
AstraZeneca will present a late-breaker abstract
on the COAST Phase 2 trial, highlighting progression-free survival
(PFS) results for novel durvalumab combinations with potential new
medicines, including Innate’s monalizumab, and oleclumab, an
anti-CD73 monoclonal antibody, in unresectable, Stage III non-small
cell lung cancer (NSCLC). Monalizumab, Innate’s lead
partnered asset, is a potentially first-in-class immune checkpoint
inhibitor targeting NKG2A receptors expressed on tumor infiltrating
cytotoxic CD8+ T cells and NK cells.
In addition, Innate will present pre-clinical
data from its next-generation, proprietary, multi-specific NK cell
engager platform known as ANKETTM (Antibody-based
NK cell Engager
Therapeutics).
“We’re pleased with the continued progress of
monalizumab, particularly in a combination trial with durvalumab in
unresectable, Stage III non-small cell lung cancer,”
said Mondher Mahjoubi, Chief Executive
Officer of Innate Pharma. “Furthermore, the
pre-clinical ANKETTM data at ESMO validates the importance of NK
cell science and its role in the next wave of immunotherapy, while
serving as the scientific engine to further advance our clinical
pipeline. We look forward to seeing both oral presentations at
ESMO.”
Presentation details
Monalizumab:
Title: COAST: an open-label,
randomised, phase 2 platform study of durvalumab alone or in
combination with novel agents in patients with locally advanced,
unresectable, Stage III NSCLCDate and time:
September 17, 2021, at 2:20 p.m. CEST Presentation
number: LBA42
Alexandre Martinez-Marti (Barcelona, Spain) will
deliver the presentation.
ANKET:
Title: Harnessing innate
immunity in cancer therapies: the example of Natural Killer Cell
EngagersDate and time: September 18, 2021 at 1:30
p.m. CESTPresentation number: 1O
Professor Eric Vivier, DVM, Chief Scientific
Officer of Innate Pharma, will deliver the presentation.
About Monalizumab:
Monalizumab is a potentially first-in-class
immune checkpoint inhibitor targeting NKG2A receptors expressed on
tumor infiltrating cytotoxic CD8+ T cells and NK cells.
NKG2A is an inhibitory checkpoint receptor for
HLA-E. By expressing HLA-E, cancer cells can protect themselves
from killing by NKG2A+ immune cells. HLA-E is frequently
overexpressed in the cancer cells of many solid tumors and
hematological malignancies. Monalizumab may reestablish a broad
anti-tumor response mediated by NK and T cells, and may enhance the
cytotoxic potential of other therapeutic antibodies1.
AstraZeneca obtained full oncology rights to
monalizumab in October 2018 through a co-development and
commercialization agreement initiated in 2015. The ongoing
development for monalizumab is focused on investigating monalizumab
in various combination strategies in different malignancies.
About COAST Trial:
COAST is a Phase 2,
multi-arm, randomised trial
investigating durvalumab alone or in combination with
either monalizumab, an anti-NKG2A monoclonal antibody, or
oleclumab, an anti-CD73 monoclonal antibody, in 189 patients
with locally advanced, unresectable Stage III NSCLC who had
not progressed after concurrent CRT.
COAST is being conducted by AstraZeneca in
82 centers across nine countries in North
America, Europe and Asia. The primary endpoint of the
trial is overall response rate (ORR) as a measure
of anti-tumor activity. Secondary endpoints include
safety, duration of response, overall survival
and PFS.
About
ANKETTM:
ANKETTM (Antibody-based
NK cell Engager
Therapeutics) is Innate Pharma's proprietary
platform for developing next-generation, multi-specific NK cell
engagers to treat certain types of cancer. The Company’s latest
innovation, its tetra-specific ANKET molecule, is the first NK cell
engager technology to engage activating receptors (NKp46 and CD16),
a tumor antigen and a cytokine (IL-2v) via a single molecule. This
leverages the advantages of harnessing NK cell effector functions
against cancer cells and also provides proliferation and activation
signals targeted to NK cells.
In preclinical studies, Innate's tri-2 and
tetra-specific technology has demonstrated potent NK cell
activation, cytotoxicity and efficient control of tumor growth in
preclinical models. This versatile fit-for-purpose technology is
creating an entirely new class of molecules to induce synthetic
immunity against cancer.
About Innate Pharma:
Innate Pharma S.A. is a global, clinical-stage
oncology-focused biotech company dedicated to improving treatment
and clinical outcomes for patients through therapeutic antibodies
that harness the immune system to fight cancer.
Innate Pharma’s broad pipeline of antibodies
includes several potentially first-in-class clinical and
preclinical candidates in cancers with high unmet medical need.
Innate is a pioneer in the understanding of
Natural Killer (NK) cell biology and has expanded its expertise in
the tumor microenvironment and tumor antigens, as well as antibody
engineering. This innovative approach has resulted in a diversified
proprietary portfolio and major alliances with leaders in the
biopharmaceutical industry including Bristol-Myers Squibb, Novo
Nordisk A/S, Sanofi, and a multi-products collaboration with
AstraZeneca.
Headquartered in Marseille, France, with a US
office in Rockville, MD, Innate Pharma is listed on Euronext Paris
and Nasdaq in the US.
Learn more about Innate Pharma at
www.innate-pharma.com
Information about Innate Pharma
shares:
ISIN codeTicker
codeLEI |
FR0010331421Euronext: IPH Nasdaq: IPHA9695002Y8420ZB8HJE29 |
Disclaimer on forward-looking
information and risk factors:
This press release contains certain
forward-looking statements, including those within the meaning of
the Private Securities Litigation Reform Act of 1995. The use of
certain words, including “believe,” “potential,” “expect” and
“will” and similar expressions, is intended to identify
forward-looking statements. Although the company believes its
expectations are based on reasonable assumptions, these
forward-looking statements are subject to numerous risks and
uncertainties, which could cause actual results to differ
materially from those anticipated. These risks and uncertainties
include, among other things, the uncertainties inherent in research
and development, including related to safety, progression of and
results from its ongoing and planned clinical trials and
preclinical studies, review and approvals by regulatory authorities
of its product candidates, the Company’s commercialization efforts,
the Company’s continued ability to raise capital to fund its
development and the overall impact of the COVID-19 outbreak on the
global healthcare system as well as the Company’s business,
financial condition and results of operations. For an additional
discussion of risks and uncertainties which could cause the
company's actual results, financial condition, performance or
achievements to differ from those contained in the forward-looking
statements, please refer to the Risk Factors (“Facteurs de Risque")
section of the Universal Registration Document filed with the
French Financial Markets Authority (“AMF”), which is available on
the AMF website http://www.amf-france.org or on Innate Pharma’s
website, and public filings and reports filed with the U.S.
Securities and Exchange Commission (“SEC”), including the Company’s
Annual Report on Form 20-F for the year ended December 31, 2020,
and subsequent filings and reports filed with the AMF or SEC, or
otherwise made public, by the Company.
This press release and the information contained
herein do not constitute an offer to sell or a solicitation of an
offer to buy or subscribe to shares in Innate Pharma in any
country.
For additional information, please contact: |
InvestorsInnate
Pharma
Henry Wheeler Tel.: +33 761 88 38
74 Henry.wheeler@innate-pharma.fr |
MediaInnate Pharma Tracy Rossin
(Global/US)Tel.: +1 240 801
0076Tracy.Rossin@innate-pharma.comATCG Press Marie
Puvieux (France)Tel.: +33 (0)9 81 87 46
72innate-pharma@atcg-partners.com |
__________________________1 André et al, Cell
20182 Gauthier et al., Cell 2019
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