Cure8 news brief
Cure8 news brief
Perianal fistulas are a common, disabling complication of Crohn’s disease. A medication that provides durable fistula remission through 48 weeks could change treatment options for people with Crohn’s and perianal disease.
The report focuses on Phase 3 trial outcomes for TREMFYA (guselkumab), an IL-23 inhibitor already used in other inflammatory diseases.
Adults with Crohn’s disease, especially those with perianal fistulas; gastroenterologists and colorectal surgeons treating fistulizing disease; clinical researchers in IBD and IL-23–targeted therapies.
Johnson & Johnson (Janssen) reported positive 48-week Phase 3 (FUZION) results for TREMFYA (guselkumab) in adults with Crohn’s disease and perianal fistula.
The company states combined fistula remission (clinical + radiologic) was maintained or improved through Week 48 versus earlier timepoints, with quoted Week 24 to Week 48 increases in the 100 mg group (28% to 35%). Safety through Week 48 was described as consistent with the known profile.
This summary is based on the RTT News article reporting company-released trial results.
This article is a news report summarizing company-announced Phase 3 data (FUZION). RTT News relays J&J/Janssen’s statements; the full peer-reviewed publication or regulatory filings were not provided in the article.
Reported percentages come from the company’s press information; independent peer-reviewed confirmation and regulatory review are needed before changing clinical practice.
Review the original publication for the complete reporting, methods, and context.
This Cure8 brief is based on source text from the linked article. Cure8 is informational only and is not a substitute for professional medical advice, diagnosis, or treatment.