Treatment-emergent adverse events were comparable across all groups, with no serious events reported during the study. Three severe treatment-emergent adverse events, all of which resolved or resolved with sequelae, did occur but were deemed to be unrelated to treatment with tigulixostat.
Treatment with tigulixostat at all three doses appeared effective and well tolerated. These results and the observed safety profile support tigulixostat dose finding and the continued development of this agent for patients with gout and hyperuricemia.
ad goes here:advert-1
ADVERTISEMENT
SCROLL TO CONTINUE
Michele B. Kaufman, PharmD, BCGP, is a freelance medical writer based in New York City and a pharmacist at New York Presbyterian Lower Manhattan Hospital.
Reference
- Terkeltaub R, Mune J, Lee J, et al. Phase 2 study results from a randomized, double-blind, placebo-controlled, dose-finding study to evaluate efficacy and safety of tigulixostat, a novel non-purine selective xanthine oxidase inhibitor, in gout patients with hyperuricemia [abstract: L05]. Arthritis Rheumatol. 2021 Oct; 73(suppl 10).