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Clinical Trial Summary

The primary purpose of this study is to assess the effect of verekitug (UPB-101) on the endoscopically determined size and extend of nasal polyps in participants with chronic rhinosinusitis with nasal polyps (CRSwNP) and to assess the safety and tolerability of verekitug (UPB-101) compared to placebo.


Clinical Trial Description

This is a multicenter, randomized, placebo controlled, parallel group study to assess the efficacy and safety of verekitug (UPB-101) administered subcutaneously (SC) in participants with CRSwNP on background therapy with stable dosage of intranasal corticosteroids (INCS). Approximately 70 participants will be randomized. Participants will receive verekitug (UPB-101) or placebo over a 24-week treatment period. In addition, this study consists of a 3 to 5-week Screening Period and a 4-week Follow-up Period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06164704
Study type Interventional
Source Upstream Bio Inc.
Contact Upstream Bio Clinical Trials Information (Privacy Notice: https:
Phone 888-446-3130
Email clinicaltrials@upstreambio.com
Status Recruiting
Phase Phase 2
Start date December 18, 2023
Completion date April 2025

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