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A Study of Efficacy and Safety of TLL-018 in CSU Participants

Chronic Spontaneous Urticaria Clinical Trial

Official title:
A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of TLL-018 in Participants With Moderate-to-Severe Chronic Spontaneous Urticaria With Inadequate Controll to Second Generation H1-antihistamines

Clinical Trial Summary

A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of TLL-018 in Participants With Moderate-to-Severe Chronic Spontaneous Urticaria (CSU) With Inadequate Controll to Second Generation H1-antihistamines.

Clinical Trial Description

This is a randomized, double-blind, single-dummy, placebo-parallel-group, phase 3 study to assess the safety and efficacy of TLL-018 in Moderate-to-Severe Chronic Spontaneous Urticaria (CSU) participants who had an Inadequate Controll to Second Generation H1-antihistamines. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06396026
Study type Interventional
Source Hangzhou Highlightll Pharmaceutical Co., Ltd
Contact
Status Not yet recruiting
Phase Phase 3
Start date May 30, 2024
Completion date December 30, 2027
View Details
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