drugset / Trial / NCT04827589

Study to Evaluate the Efficacy, Safety, and Tolerability of Tirabrutinib in Participants With Antihistamine-Resistant Chronic Spontaneous Urticaria

NCT04827589

Phase 2 Withdrawn Gilead Sciences
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary objective of this study is to evaluate the efficacy of tirabrutinib in reducing disease activity in participants with chronic spontaneous urticaria (CSU) with respect to change from baseline in urticaria activity score over 7 days (UAS7) at Week 8 when added to standard of care.

Timeline

Start
2021-07
Primary completion
2022-04
Completion
2022-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Tirabrutinib Small molecule Oral