drugset / Trial / NCT05335499

A Phase 2a Study of TAS5315 in Patients With Chronic Spontaneous Urticaria

NCT05335499 ↗

Phase 2 Completed 126 enrolled Taiho Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of TAS5315 in chronic spontaneous urticaria patients with an inadequate response to H1-antihistamines

Timeline

Start
2022-06-28
Primary completion
2023-12-22
Completion
2023-12-22

Drugs

EvaluationDrugModalityDoseRoute
Subject TAS5315 Unknown — Oral