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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy, safety and pharmacokinetics of GDC-0853 compared with placebo in participants with Refractory Chronic Spontaneous Urticaria (CSU) already treated with anti-histamines. Participants have the option to enter the Open-Label Extension (OLE) study after completing the 8-week treatment period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03137069
Study type Interventional
Source Genentech, Inc.
Contact
Status Completed
Phase Phase 2
Start date May 26, 2017
Completion date October 25, 2019

See also
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