Eli Lilly's Omvoh Surpasses J&J's Stelara in Crohn's Disease Phase III Trial

Eli Lilly's Omvoh has demonstrated superior long-term outcomes compared to Johnson & Johnson's Stelara in the treatment of Crohn's disease, as shown in the Phase III VIVID-1 trial. At the 52-week mark, Omvoh exhibited a nominally statistically significant better histologic response, including among patients with previous biologic treatment failures, according to ECCO mucosal histopathology criteria[1][2]. Omvoh’s mechanism involves selectively targeting the IL-23 cytokine, which plays a crucial role in reducing mucosal inflammation[1]. These results support Eli Lilly's regulatory submissions to expand Omvoh's label, potentially strengthening its market position amidst the growing competition from Stelara biosimilars[1][2].
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What are the specific mechanisms that make Omvoh superior to Stelara in treating Crohn's disease?
How might the entry of Omvoh impact the market competition between Eli Lilly and biosimilars?
What potential regulatory hurdles could Eli Lilly face in expanding Omvoh's label for Crohn's disease?
How do the efficacy and safety profiles of Omvoh compare to those of existing treatments for inflammatory bowel disease?
What strategic plans does Eli Lilly have to strengthen Omvoh's position in the inflammatory bowel disease market?