Condition: Asthma · Sponsor: Novartis Pharmaceuticals
The purpose of this study is to characterize the bronchodilator effect, systemic exposure and safety/tolerability of two different doses of inhaled glycopyrronium, when compared to placebo. Outcome of this study will be used to determine the dose of inhaled glycopyrronium for the development of fixed dose combination indacaterol/mometasone/glycopyrronium (QVM149) for children aged 6 to less than 12 years old with moderate to severe asthma.
This description comes directly from the study's public registry record.
Novartis Pharmaceuticals · +41613241111 · novartis.email@novartis.com
Novartis Pharmaceuticals
Always discuss trial participation with your own doctor first.
| Novartis Investigative Site | Rousse, Bulgaria | Recruiting |
| Novartis Investigative Site | Sevlievo, Bulgaria | Recruiting |
| Novartis Investigative Site | Sofia, Bulgaria | Recruiting |
| Novartis Investigative Site | Ibague, Tolima Department, Colombia | Recruiting |
| Novartis Investigative Site | Guatemala City, GTM, Guatemala | Withdrawn |
| Novartis Investigative Site | Guatemala City, Guatemala | Recruiting |
| Novartis Investigative Site | Debrecen, Hajdu Bihar Megye, Hungary | Recruiting |
| Novartis Investigative Site | Budapest, Hungary | Recruiting |
| Novartis Investigative Site | Budapest, Hungary | Recruiting |
| Novartis Investigative Site | Eger, Hungary | Recruiting |
| Novartis Investigative Site | Kaposvár, Hungary | Withdrawn |
| Novartis Investigative Site | Nagykanizsa, Hungary | Withdrawn |
+ 11 more locations — full list on the registry record.
Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.
We email about this public record only. Unsubscribe anytime with one click. Never medical advice.
This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT05222529