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Clinical Trial Summary

The study is a Phase II, multicenter, randomized, double-blind study to evaluatethe efficacy and safety of LP-003 administered subcutaneously as an add-on therapy for the treatment of adult patients aged 18-75 who have been diagnosed with refractory CSU and who remain symptomatic despitestandard-dose H1 antihistamine treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06228560
Study type Interventional
Source Longbio Pharma
Contact Hongzhou Yang
Phone 021-58372390
Email yanghz@longbio.com
Status Recruiting
Phase Phase 2
Start date January 25, 2024
Completion date January 30, 2025

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