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 in Healthy Adult Participants

Status: Completed

Phase of Trial: Phase I

Latest Information Update: 12 Jun 2025

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At a glance

05 Jun 2025 Status changed from active, no longer recruiting to completed.
25 May 2025 Planned End Date changed from 30 Jun 2025 to 2 Jun 2025.
25 May 2025 Planned primary completion date changed from 30 Jun 2025 to 2 Jun 2025.

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