CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 22 enrolled
Drug / intervention
Budesonide/Glycopyrronium/Formoterol (BGF) +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06905483
NCT06905483Phase 4Completed

Comparative Effects of Triple Inhaled Therapy With Budesonide/Glycopyrronium/Formoterol Versus Fluticasone Furoate/Umeclidinium/Vilanterol on Small Airway Disease in COPD Patients: A Randomized Crossover Study

Thammasat University·interventional·Posted Apr 1, 2025·Updated Feb 2, 2026

In Brief

A Phase 4 clinical trial evaluating Budesonide/Glycopyrronium/Formoterol (BGF) and Fluticasone Furoate/Umeclidinium/Vilanterol (FUV) for COPD and 4 related conditions. Completed, enrolled 22 participants across 1 site.

Detailed Summary

The goal of this clinical trial is to determine if triple inhaled therapy with Budesonide/Glycopyrronium/Formoterol (BGF) and Fluticasone Furoate/Umeclidinium/Vilanterol (FUV) are effective in treating patients with stable chronic obstructive pulmonary disease (COPD). It will also assess the safety of both drugs. The main questions it aims to answer are: * Does BGF demonstrate a comparable effect to FUV in COPD participants? * What medical problems do participants experience when taking BGFand FUV?

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesThailand
Collaborators--

Timeline

Phase 4CompletedFinished
2026
First PostedApr 1, 2025
Enrollment StartApr 1, 2025
Primary CompletionDec 31, 2025
Study CompletionJan 28, 2026
TodayJul 1, 2026
Enrollment to primary: 9 monthsPosted 1.3 years ago

Interventions

Budesonide/Glycopyrronium/Formoterol (BGF)drug

Each patient received 4 weeks of treatment with either BGF or FUV followed by a 1-week washout period, and then 4 weeks of treatment with the other drug.

Fluticasone Furoate/Umeclidinium/Vilanterol (FUV)drug

Each patient received 4 weeks of treatment with either BGF or FUV followed by a 1-week washout period, and then 4 weeks of treatment with the other drug.