Can a smart inhaler deliver better asthma care for kids?
NCT ID NCT06290102
First seen Aug 04, 2026 · Last updated Aug 05, 2026 · Updated 1 time
Summary
This trial is testing a new inhaler that combines two asthma medications—fluticasone propionate and albuterol sulfate—in a single device with an electronic module. The study involves children aged 4 to 11 with stable asthma. The goal is to measure how much of the medication gets into the body and to compare it with an existing inhaler. The study also checks for any side effects.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
- Active substance
- fluticasone propionate and albuterol sulfate combination inhaler
- What this could lead to
- If successful, this could lead to a more convenient and effective inhaler for children with asthma, potentially improving symptom control.
- What could go wrong
- This is an early-stage trial with a small number of participants, so results may not apply to all children. The study focuses on drug levels and safety, not long-term effectiveness.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Teva Investigational Site 12001
Boerne, Texas, 78006, United States
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Teva Investigational Site 12002
Miami, Florida, 33155, United States
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Teva Investigational Site 12003
Long Beach, California, 90815, United States
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Teva Investigational Site 12005
Miami, Florida, 33142, United States
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Teva Investigational Site 12007
Miami, Florida, 33130, United States
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Teva Investigational Site 12008
Lafayette, Louisiana, 70508, United States
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Teva Investigational Site 12009
San Antonio, Texas, 78249, United States
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Teva Investigational Site 12010
Mobile, Alabama, 36608, United States
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Teva Investigational Site 12011
Columbia, Missouri, 65203, United States
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Teva Investigational Site 12012
Oklahoma City, Oklahoma, 73120-9389, United States
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Other studies related to the condition(s) this trial covers.
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