Trial Profile

A Randomized, Double-Blind, Parallel Group, Multicenter 24 Week Study to Assess the Efficacy and Safety of Budesonide and Formoterol Fumarate Metered Dose Inhaler Relative to Budesonide Metered Dose Inhaler and Open-Label Symbicort Turbuhaler in Participants with Inadequately Controlled Asthma (VATHOS)

Status: Completed

Phase of Trial: Phase III

Latest Information Update: 08 May 2025

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At a glance

02 May 2025 Primary endpoint (United States (US): Change from baseline in forced expiratory volume in 1 second (FEV1) area under the curve 0 to 3 hours (AUC0-3) at Week 24) has been met.
02 May 2025 Results presented in the AstraZeneca Media Release.
25 Mar 2025 Status changed from active, no longer recruiting to completed.

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