Trial Profile

A Phase I, Randomized, Double-blind, Single-dose, Partial-replicate, 3-way Cross-over Study to Assess the Total Systemic Exposure Bioequivalence of Budesonide, Glycopyrronium, and Formoterol Delivered by BGF MDI HFO Compared With BGF MDI HFA

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 01 May 2025

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At a glance

Drugs Budesonide/formoterol/glycopyrrolate (Primary) ; Budesonide/formoterol/glycopyrrolate (Primary)
Indications Chronic obstructive pulmonary disease
Focus Pharmacokinetics
Sponsors AstraZeneca

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