OSE OSE Immunotherapeutics SA

OSE Immunotherapeutics Presents Three Abstracts for Anti-IL-7R mAb Lusvertikimab in Ulcerative Colitis at the 20th Congress of ECCO

OSE Immunotherapeutics Presents Three Abstracts for Anti-IL-7R mAb Lusvertikimab in Ulcerative Colitis at the 20th Congress of ECCO

OSE Immunotherapeutics Presents Three Abstracts for Anti-IL-7R mAb Lusvertikimab in Ulcerative Colitis at the 20th Congress of ECCO

NANTES, France - January 28 2025, – 7:30am CET - OSE Immunotherapeutics SA (ISIN: FR0012127173; Mnemo: OSE), shares details of the three scientific abstracts on its anti-IL-Receptor (IL-7R) Lusvertikimab, which is in clinical development for ulcerative colitis. These abstracts will be presented in Oral Presentation, Digital Oral Presentation and Poster Presentation at the upcoming 20th Congress of ECCO (European Crohn’s and Colitis Organization) to be held February 19-22, 2025, in Berlin (Germany).

Nicolas Poirier, Chief Executive Officer of OSE Immunotherapeutics, comments: “With three abstracts accepted for presentation at ECCO 2025, we look forward to sharing new preclinical and clinical efficacy data on Lusvertikimab with the world’s leading specialists in Inflammatory Bowel Diseases (IBD).”

Presentation Details:

Oral presentation
TitlePresenterSessionDate and time
OP36 -  Arnaud BourreilleSession name: Sustainability in IBD and beyond Session 10: Hot topics in IBD

Session hall: Plenary Hall / Hall B
Session date: February 20, 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.



Digital oral presentation
TitlePresenterSessionDate and time
DOP031 - Nicolas PoirierSession name: DOP Session 4:

Novel targets in IBD

Session hall: A5
Session date:

February 20, 2025​

Session time:

17:45 - 18:45

Presentation time:

18:03 - 18:09​



Poster presentation
TitlePresenterSession Date and time
PO916 – Walter ReinishPoster 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: .

Follow us on X and LinkedIn



Contacts

Fiona Olivier









Sylvie Détry













French Media Contact

FP2COM

Florence Portejoie



+33 6 07 768 283







U.S. Media Contact

Rooney Partners LLC

Kate Barrette







 

Forward-looking statements

This press release contains express or implied information and 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.

These forward-looking statements include statements typically using conditional and containing verbs such as “expect”, “anticipate”, “believe”, “target”, “plan”, or “estimate”, their declensions and conjugations and words of similar import. Although the OSE Immunotherapeutics management believes that the 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.

Attachment



EN
28/01/2025

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on OSE Immunotherapeutics SA

 PRESS RELEASE

OSE Immunotherapeutics Receives Second Positive IDMC Recommendation fo...

OSE Immunotherapeutics Receives Second Positive IDMC Recommendation for Phase 3 ARTEMIA Trial Evaluating Tedopi® in Non-Small Cell Lung Cancer NANTES, France, February 26, 2026 – 6pm CET - OSE Immunotherapeutics SA (ISIN: FR0012127173; Mnemo: OSE), today announced that the Independent Data Monitoring Committee (IDMC) has issued a second positive recommendation for the ongoing pivotal Phase 3 ARTEMIA trial evaluating Tedopi® in advanced non-small cell lung cancer (NSCLC). The IDMC advised that the study should continue as planned, with no protocol changes. In line with the predefined study ...

 PRESS RELEASE

OSE Immunotherapeutics reçoit un deuxième avis positif du Comité Indép...

OSE Immunotherapeutics reçoit un deuxième avis positif du Comité Indépendant de Surveillance des Données (IDMC) pour l’essai pivot de Phase 3 ARTEMIA évaluant Tedopi® dans le cancer du poumon non à petites cellules Nantes, le 26 février 2026 – 18h00 CET - OSE Immunotherapeutics SA (ISIN: FR0012127173; Mnémo : OSE) annonce aujourd’hui que le Comité Indépendant de Surveillance des Données (IDMC) a émis une deuxième recommandation positive concernant l’essai pivot de Phase 3 ARTEMIA en cours, évaluant Tedopi® dans le cancer du poumon non à petites cellules (CPNPC) à un stade avancé. L’IDMC a r...

 PRESS RELEASE

OSE Immunotherapeutics Selects Chronic Pouchitis and Hidradenitis Supp...

OSE Immunotherapeutics Selects Chronic Pouchitis and Hidradenitis Suppurativa as New Key Indications for Lusvertikimab OSE Immunotherapeutics Selects Chronic Pouchitis and Hidradenitis Suppurativa as New Key Indications for Lusvertikimab Development built on strong IL-7R biological rationaleChronic Pouchitis offers a capital-efficient rare-disease path with fast route to marketHidradenitis Suppurativa enables rapid proof-of-concept in a large dermatology marketFirst Phase 2 clinical trial expected to start in H2 2026, subject to financingUlcerative Colitis remains a key indication to be pa...

 PRESS RELEASE

OSE Immunotherapeutics sélectionne la pouchite chronique et l’hidradén...

OSE Immunotherapeutics sélectionne la pouchite chronique et l’hidradénite suppurée comme nouvelles indications clés pour Lusvertikimab OSE Immunotherapeutics sélectionne la pouchite chronique et l’hidradénite suppurée comme nouvelles indications clés pour Lusvertikimab Développement basé sur un fort rationnel biologique de l’IL-7RLa pouchite chronique offre une opportunité de développement dans une maladie rare à un coût limité et une possible mise sur le marché rapideL'hidradénite suppurée permet une preuve de concept rapide sur un vaste marché dermatologiqueUn premier essai clinique de...

 PRESS RELEASE

OSE Immunotherapeutics Welcomes FDA Orphan Drug Designation Granted to...

OSE Immunotherapeutics Welcomes FDA Orphan Drug Designation Granted to Pegrizeprument (VEL-101) OSE Immunotherapeutics Welcomes FDA Orphan Drug Designation Granted to Pegrizeprument (VEL-101) Nantes, France, January 21, 2026 – 6pm CET - OSE Immunotherapeutics SA (ISIN: FR0012127173; Mnemo: OSE), today acknowledges the announcement by its partner Veloxis Pharmaceuticals, Inc. that the U.S. Food and Drug Administration (FDA) has granted Orphan Drug Designation to pegrizeprument (VEL-101) for the prevention of organ rejection in patients undergoing liver transplantation. Veloxis’ full press ...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch