HFA-152a vs HFA-134a Inhaler Propellants for Asthma
What You Need to Know Before You Apply
What is the purpose of this trial?
This study aims to generate additional safety data on the propellant component of the reformulated product by comparing metered dose inhaler (MDIs) containing HFA-152a (test) with HFA-134a (reference).
Who Is on the Research Team?
GSK Clinical Trials
Principal Investigator
GlaxoSmithKline
Are You a Good Fit for This Trial?
This trial is for adults (18 or older) with a documented history of asthma who use inhalers as needed, possibly along with other common asthma medications. Participants must be stable on their current treatment and meet specific medication use patterns.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Trial Overview
The study compares the safety of two different propellants used in metered dose inhalers: HFA-152a (new) versus HFA-134a (standard), over a period of four weeks in people with asthma.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Participants will receive HFA-152a MDI in treatment period 1 followed by HFA-134a MDI in treatment period 2. There will be a washout period between the treatment periods.
Participants will receive HFA-134a MDI in treatment period 1 followed by HFA-152a MDI in treatment period 2. There will be a washout period between the treatment periods.
Find a Clinic Near You
Who Is Running the Clinical Trial?
GlaxoSmithKline
Lead Sponsor
Dame Emma Walmsley
GlaxoSmithKline
Chief Executive Officer since 2017
MA in Classics and Modern Languages from Oxford University
Dr. Hal Barron
GlaxoSmithKline
Chief Medical Officer since 2018
MD from Harvard Medical School
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