drugset / Trial / NCT06164704

A Study to Investigate the Efficacy and Safety of Verekitug (UPB-101) in Participants With Chronic Rhinosinusitis With Nasal Polyps

NCT06164704 ↗

Phase 2 Completed 81 enrolled Upstream Bio Inc.
RandomizedParallel-groupQuadruple-blindTreatment

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.

Timeline

Start
2023-12-18
Primary completion
2025-07-07
Completion
2025-07-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Verekitug Monoclonal antibody 100 mg Subcutaneous