French biotechnology company OSE Immunotherapeutics SA (Euronext Paris:OSE) said on Thursday that it has selected chronic pouchitis and hidradenitis suppurativa as new key clinical indications for its IL-7R antagonist lusvertikimab (OSE-127).
This aligns with the company's 2026-2028 strategic plan to expand into targeted immune-mediated diseases.
OSE Immunotherapeutics plans to initiate its first Phase 2 trial in the second half of 2026, subject to financing, while continuing to seek a partner for the ulcerative colitis programme and advancing a subcutaneous formulation. Management cited strong IL-7R biological rationale and prior statistically significant Phase 2 efficacy and favourable safety data in ulcerative colitis as supporting factors.
Chronic pouchitis was identified as a capital-efficient rare-disease opportunity with a defined patient population and limited competition, affecting an estimated 45,000 chronic cases across the European Union, North America, and Japan. Hidradenitis suppurativa represents a larger dermatology market with rapid proof-of-concept potential, impacting around 1% of the general population, or about 9.5 million individuals across the same regions, with 0.5-0.6 million moderate-to-severe patients potentially eligible for biologic therapy. The company stated that both indications exhibit T-cell driven inflammation and elevated IL-7R pathway activity, supporting a differentiated immunology platform strategy and multi-indication commercialisation potential.
AFYREN ingredient enables global launch of natural propionic acid skincare product
Merck reports positive Phase 2b results for tulisokibart in hidradenitis suppurativa
Genentech's fenebrutinib receives FDA priority review for multiple sclerosis
BRC Therapeutics participates in regulators' workshop advancing botanical drug development
Ascletis reports positive results from ASC50 clinical study for treatment of plaque psoriasis
XtalPi submits US FDA IND application for KQTD-126 in chronic intestinal pain
AbbVie secures EU approval for RINVOQ in polyarticular juvenile idiopathic arthritis
Altesa BioSciences presents positive vapendavir clinical data at ERS International Congress 2026
Kali Therapeutics' KT501 Investigational New Drug application cleared by US FDA
Teva reports positive Phase 2a data for TEV '408 in celiac disease
AbbVie seeks EMA approval for subcutaneous induction of risankizumab in Crohn's disease
AstraZeneca and Amgen report Tezspire met primary endpoints in Phase III EoE trial
Oxcia receives EMA orphan designation for OXC-201 in idiopathic pulmonary fibrosis
Graviton BioScience reports positive trial results for GV101 in chronic Graft versus Host Disease