OSE Immunotherapeutics Presents Positive Preclinical Data on Combination of Anti-IL-7 Receptor Lusvertikimab in Chronic Colitis In Oral Presentation at 20th Congress of ECCO
20 Février 2025 - 6:05PM
UK Regulatory
OSE Immunotherapeutics Presents Positive Preclinical Data on
Combination of Anti-IL-7 Receptor Lusvertikimab in Chronic Colitis
In Oral Presentation at 20th Congress of ECCO
OSE Immunotherapeutics Presents Positive
Preclinical Data on Combination of Anti-IL-7 Receptor Lusvertikimab
in Chronic Colitis
In Oral Presentation at
20th Congress of
ECCO
NANTES, France – February 20, 2025,
6:00pm CET - OSE Immunotherapeutics SA (ISIN: FR0012127173; Mnemo:
OSE), today presented positive preclinical data on the
combination of anti-IL-7 receptor (IL-7R) with anti-IL-12/23
monoclonal antibody (mAb) in chronic colitis at the 20th
Congress of ECCO (European Crohn’s and Colitis Organization), held
from February 19-22, 2025, in Berlin (Germany).
The oral communication, entitled “Anti-IL-7
Receptor Plus Anti-IL12/23 Combination Induces Complete
Histological Normalization in Chronic Colitis”, presented by
Nicolas Poirier, reported that
IL-7 drives resistance to anti-IL-23 inhibition. The administration
of anti-IL-7R in combination with an anti-IL-12/23 acts
synergistically to achieve profound preclinical control of chronic
colitis, characterized by complete histological healing.
Nicolas Poirier, CEO of OSE
Immunotherapeutics, comments: “Our latest research
shows that IL-7 prevents the inhibitory effect of IL-23 antagonists
on the control of human Th17 T lymphocytes. Additionally, IL-7R
overexpression in the colon of ulcerative colitis or Crohn’s
disease patients correlates with high IL-23 expression. We
demonstrated that combining anti-IL-7R with anti-IL-12/23 mAb is
well tolerated and synergizes to control chronic colitis symptoms
in a validated preclinical model. It also demonstrates complete
histological normalization compared to monotherapies.
“Together with the positive efficacy seen in
the Phase 2 Lusvertikimab monotherapy clinical results on
endoscopic and histological remission in ulcerative colitis, to be
presented in the Top-10 highlighted plenary session at ECCO, these
latest preclinical data for the combination of the inhibition of
upstream (IL-7) and downstream (IL-23) inflammatory mechanisms
expand and strengthen the potential positioning of our
first-in-class drug candidate in the Immuno-Inflammation (I&I)
therapeutic landscape. I would like to warmly thank the OSE
research, translational, computational biology and clinical teams
for their coordinated efforts in achieving these significant
milestones.”
More details on the
presentation:
- Interleukin-7
(IL-7) drives not only the survival but also the differentiation of
human T lymphocytes subsets, such as Th17 (IL-17-secreting
pathogenic T lymphocytes). IL-23 is the primary driver of Th17
differentiation, and IL-23 antagonists (currently one of the
standards of care in Inflammatory Bowel Diseases [IBD]) inhibit the
generation of Th17 cells. However, in the presence of IL-7, IL-23
antagonists lose their inhibitory activity in vitro.
Combining Lusvertikimab with an anti-IL-23 monoclonal antibody (eg.
Guselkumab) restores the inhibition of human Th17 cells in the
presence of both IL-7 and IL-23.
- High IL-7R
tissue expression has previously been observed in the colon of IBD
patients with resistance to anti-TNF or anti-integrin
therapies1. OSE Immunotherapeutics’ R&D team has
shown that IL-7R is also overexpressed in the mucosa of patients
with resistance to anti-IL-12/23 antagonist therapy, and that IL-7R
expression correlates with high mucosal IL-23 expression.
- Using a
well-validated preclinical chronic colitis model, OSE
Immunotherapeutics’ R&D team reported that while the IL-12/23
antagonist mAb is efficient, it is not sufficient in monotherapy to
achieve complete remission at both macroscopic and histological
levels. In contrast, the combination of anti-IL-7R mAb and
anti-IL-12/23 mAb has been shown to induce significant reduction of
all colitis symptoms (e.g. macroscopic colon weight and length
ratio) as well as complete microscopic histological remission and
normalization, with no histological lesions, immune cell
infiltrates, or epithelial cell hyperplasia. Additionally, a
significant decrease in T-lymphocyte immuno-staining was observed
in the colon, along with a significant increase in the Foxp3+ to
Treg ratio, confirming the original mechanism of action of the
IL-7R antagonist.
Upcoming oral and poster
presentations at ECCO’25 congress:
Oral Presentation |
|
|
|
Title |
Presenter |
Session |
Date and time |
OP36 - "LUSVERTIKIMAB, A FIRST-IN-CLASS
IL7 RECEPTOR ANTAGONIST, IN MODERATE TO SEVERE ULCERATIVE COLITIS:
RESULTS OF A MULTICENTER, RANDOMIZED, PLACEBO-CONTROLLED PHASE II
STUDY " |
Arnaud Bourreille |
Session name: Sustainability in IBD and beyond Session 10: Hot
topics in IBD
Session hall: Plenary Hall / Hall B |
Session date: February 22, 2025 Session time:
08:30 -10:50
Presentation time:
10:10 - 10:20 |
Selected amongst the Top 10 oral abstracts for 20th
Congress of European Crohn’s and Colitis Organization (ECCO)
Highlights. |
Poster Presentation |
|
|
Title |
Presenter |
Session |
PO916 – “LUSVERTIKIMAB IS EFFICACIOUS IN
SEVERE ULCERATIVE COLITIS (UC) PATIENTS WITH HIGH FECAL
CALPROTECTIN (FCP): RESULTS FROM THE COTIKIS STUDY” |
Walter Reinisch |
Poster sessions:
February 20, 2025, 10:30 to 18:00
February 21, 2025, 08:00 to 18:00
February 22, 2025, 09:00 to
13:00
Guided poster session:
February 21, 2025, 12:40-13:40 |
ABOUT OSE IMMUNOTHERAPEUTICS
OSE Immunotherapeutics is a biotech company
dedicated to developing first-in-class assets in immuno-oncology
(IO) and immuno-inflammation (I&I) that address the unmet
patient needs of today and tomorrow. We partner with leading
academic institutions and biopharmaceutical companies in our
efforts to develop and bring to the market transformative medicines
for people with serious diseases. OSE Immunotherapeutics is based
between Nantes and Paris and is quoted on Euronext.
Additional information about OSE
Immunotherapeutics assets is available on the Company’s website:
www.ose-immuno.com. Follow us on X and LinkedIn
Contacts
Fiona
Olivier
fiona.olivier@ose-immuno.com
Sylvie Détry
sylvie.detry@ose-immuno.com
|
France
Media Contact
FP2COM
Florence Portejoie
fportejoie@fp2com.fr
+33 6 07 768 283
U.S. Media Contact
Rooney Partners LLC
Kate Barrette
kbarrette@rooneypartners.com
+1 212 223 0561
|
|
Forward-looking statements
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statements that might be deemed forward-looking information and
statements in respect of OSE Immunotherapeutics. They do not
constitute historical facts. These information and statements
include financial projections that are based upon certain
assumptions and assessments made by OSE Immunotherapeutics’
management considering its experience and its perception of
historical trends, current economic and industry conditions,
expected future developments and other factors they believe to be
appropriate.
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statements typically using conditional and containing verbs such as
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forward-looking statements and information are reasonable, the OSE
Immunotherapeutics’ shareholders and other investors are cautioned
that the completion of such expectations is by nature subject to
various risks, known or not, and uncertainties which are difficult
to predict and generally beyond the control of OSE
Immunotherapeutics. These risks could cause actual results and
developments to differ materially from those expressed in or
implied or projected by the forward-looking statements. These risks
include those discussed or identified in the public filings made by
OSE Immunotherapeutics with the AMF. Such forward-looking
statements are not guarantees of future performance. This press
release includes only summary information and should be read with
the OSE Immunotherapeutics Universal Registration Document filed
with the AMF on April 30, 2024, including the annual financial
report for the fiscal year 2023, available on the OSE
Immunotherapeutics’ website. Other than as required by applicable
law, OSE Immunotherapeutics issues this press release at the date
hereof and does not undertake any obligation to update or revise
the forward-looking information or statements.
1 Belarif L et al.IL-7 receptor influences anti-TNF
responsiveness and T cell gut homing in inflammatory bowel disease.
Journal of Clinical Investigation 2019
- EN_250220_ECCO Preclinical presentation
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