drugset / Trial / NCT05032157

A Phase 3 Study of Efficacy and Safety of Remibrutinib in the Treatment of CSU in Adults Inadequately Controlled by H1-antihistamines

NCT05032157 ↗

Phase 3 Completed 455 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study was to establish the efficacy, safety, and tolerability of Remibrutinib 25 mg b.i.d. in adult patients suffering from chronic spontaneous urticaria (CSU) inadequately controlled by second generation H1-antihistamines (H1-AHs) in comparison to placebo.

Timeline

Start
2021-12-01
Primary completion
2023-12-18
Completion
2024-01-05

Outcome

Met primary endpoint

registry analysis (superiority test); LOU064 25 mg b.i.d. vs Placebo; p < 0.001; Mean Difference (Final Values) -7.68 (95% CI -9.91 to -5.46) NCT05032157 ↗

registry analysis (superiority test); LOU064 25 mg b.i.d. vs Placebo; p <0.001; Mean Difference (Final Values) -3.23 (95% CI -4.29 to -2.16) NCT05032157 ↗

registry analysis (superiority test); LOU064 25 mg b.i.d. vs Placebo; p < 0.001; Mean Difference (Final Values) -4.47 (95% CI -5.71 to -3.23) NCT05032157 ↗

release “The Phase III REMIX-1 and REMIX-2 studies met all primary and secondary endpoints, showing rapid, clinically meaningful improvements across urticaria disease activity scores” novartis.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Remibrutinib Small molecule 25 mg —