Home > Gastroenterology > UEGW 2024 > IBD: New Drugs, Established Agents, and Prevention > Tamuzimod delivers promising long-term data in UC

Tamuzimod delivers promising long-term data in UC

Presented by
Prof. Silvio Danese, Vito-Salute San Raffaele University, Italy
Conference
UEGW 2024
Trial
Phase 2
Doi
https://doi.org/10.55788/aafc1516
Tamuzimod was associated with improved clinical, endoscopic, and histologic outcomes compared with placebo in participants with moderately to severely active ulcerative colitis (UC) at week 52 of a phase 2 study. Moreover, the drug had a favourable safety profile.

The selective S1PR1 modulator tamuzimod displayed encouraging efficacy and safety data as induction therapy for patients with UC [1]. Prof. Silvio Danese (Vito-Salute San Raffaele University, Italy) presented the long-term extension data of the phase 2 study evaluating tamuzimod [2]. In this randomised, double-blind controlled study (NCT05156125), participants with moderately to severely active UC (n=213) were assigned in a 1:1:1 ratio to receive tamuzimod 60 mg, tamuzimod 30 mg, or a placebo. After 13 weeks, those who achieved a clinical response (n=95) were eligible for maintenance therapy with the previously assigned treatment. Also, participants on placebo who lost response during the long-term extension were allowed to switch to the open-label extension phase and received tamuzimod 60 mg. “All efficacy outcomes were based on non-responder imputation,” mentioned Prof. Danese.

At week 52, the clinical remission rates were 50% in both tamuzimod arms and 18.2% in the placebo arm (P=0.021; P=0.0078). Endoscopic remission was documented in 46.4% of participants in the 60 mg arm, 43.8% in the 30 mg arm, and 18.2% in the placebo arm (P=0.076; P=0.032). In addition, endoscopic and histologic remission was observed in 25%, 37.5%, and 9.1% of participants in the 60 mg, 30 mg, and placebo arms, respectively (P=0.18; P=0.019). “The drug was very safe, and there were no major adverse events,” according to Prof. Danese. “This is probably due to the high selectivity of tamuzimod,” he argued.

“Maintenance treatment with either 30 mg or 60 mg of tamuzimod was efficacious and well-tolerated for up to 52 weeks, supporting the continued development of tamuzimod as a treatment for patients with UC,” concluded Prof. Danese.


    1. Sands BE, et al. Gastroenterology. 2024;166:S-240.
    2. Danese S, et al. Efficacy and safety of tamuzimod in moderately to severely active ulcerative colitis through 52 weeks: phase 2 long-term extension data. LB14, UEG Week 2024, 12–15 October, Vienna, Austria.

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