drugset / Trial / NCT06196879

A Study to Investigate the Efficacy and Safety of Verekitug (UPB-101) in Adult Participants With Severe Asthma (VALIANT)

NCT06196879 ↗

Phase 2 Completed 479 enrolled Upstream Bio Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of verekitug (UPB-101) in participants with severe asthma. The study will evaluate the incidence of asthma exacerbations, other pharmacodynamic (PD) parameters such as lung function and asthma control, and the safety and tolerability of verekitug (UPB-101) compared to placebo.

Timeline

Start
2024-02-27
Primary completion
2025-12-16
Completion
2026-03-19

Drugs

EvaluationDrugModalityDoseRoute
Subject Verekitug Monoclonal antibody 100 mg Subcutaneous
Subject Verekitug Monoclonal antibody 400 mg Subcutaneous

Indications