CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 88 enrolled
Drug / intervention
QVA149 +1 moredrug
Likely dose
QVA149 50 µgfrom 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/NCT02125734
NCT02125734Phase 4Completed

A Randomized, Multicenter, Open-label, Cross-over Study to Assess Lung Function and Patient Preference After a 4 Week Treatment Each With QVA149 vs. Tiotropium in Patients With Stable Chronic Obstructive Pulmonary Disease (COPD) and Moderate to Severe Airflow Limitation Who Are on a Tiotropium Therapy (FAVOR Study)

Novartis Pharmaceuticals·interventional·Posted Apr 29, 2014·Updated Apr 12, 2017

In Brief

A Phase 4 clinical trial evaluating QVA149 and Tiotropium for Chronic Obstructive Pulmonary Disease and COPD. Completed, enrolled 88 participants across 18 sites.

Detailed Summary

The study is a multicenter, randomized, 2-period, open-label, two arm, cross-over study to show the superior effect of a 4 week treatment each with QVA149 versus tiotropium on lung function. Similarly, this study aims to evaluate patient preference after experiencing both treatment regimens in patients with a clinical diagnosis of COPD (GOLD 2013) and a moderate to severe airflow limitation who are symptomatic (defined as CAT score of at least 10) at screening despite being treated with tiotropium

Study Details

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

Timeline

Phase 4CompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedApr 29, 2014
Enrollment StartApr 1, 2014
Primary CompletionJan 1, 2015
TodayJul 2, 2026
Enrollment to primary: 9 monthsPosted 12.2 years ago

Interventions

QVA149drug

QVA149 capsules 110/50 µg for inhalation via Concep-1-inhaler device, taken once a day

Tiotropiumdrug

Tiotropium 18 µg capsules for inhalation via HandiHaler device taken once a day