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Study identifier: NCT05222529 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Pharmacokinetics, Pharmacodynamics, Safety and Tolerability of Glycopyrronium (Bromide) in Children (6 to Less Than 12 Years) With Asthma

Condition: Asthma  ·  Sponsor: Novartis Pharmaceuticals

PhasePhase 2
Planned participants42
Who can joinAll sexes, 6 Years to 11 Years
Healthy volunteersNo

About this study

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.

Talk to the study team

Novartis Pharmaceuticals  ·  +41613241111  ·  novartis.email@novartis.com

Novartis Pharmaceuticals

Always discuss trial participation with your own doctor first.

Locations (23)

Novartis Investigative SiteRousse, BulgariaRecruiting
Novartis Investigative SiteSevlievo, BulgariaRecruiting
Novartis Investigative SiteSofia, BulgariaRecruiting
Novartis Investigative SiteIbague, Tolima Department, ColombiaRecruiting
Novartis Investigative SiteGuatemala City, GTM, GuatemalaWithdrawn
Novartis Investigative SiteGuatemala City, GuatemalaRecruiting
Novartis Investigative SiteDebrecen, Hajdu Bihar Megye, HungaryRecruiting
Novartis Investigative SiteBudapest, HungaryRecruiting
Novartis Investigative SiteBudapest, HungaryRecruiting
Novartis Investigative SiteEger, HungaryRecruiting
Novartis Investigative SiteKaposvár, HungaryWithdrawn
Novartis Investigative SiteNagykanizsa, HungaryWithdrawn

+ 11 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05222529