A Study to Assess and Compare Safety and Tolerability of 3 Months Treatment With Salbutamol Administered Via MDI Containing Propellant HFA-152a or HFA-134a in Participants 12 Years of Age and Older With Asthma
- Disease/Condition
- Asthma
- Drug/Device/Intervention
- Salbutamol HFA-134a
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- GlaxoSmithKline
- Location
- Aventura,Clearwater,Edgewater,Miami,Winter Park,Rincon,Louisville,Owensboro,Minneapolis,Olive Branch,Columbia,Jersey City,Riverdale,Brooklyn,Asheville,Cincinnati,Dublin,Medford,DuBois,Philadelphia,Pit, Argentina,Canada,France,Greece,Italy,Panama,Poland,United Kingdom,United States of America
- Phase
- Phase 3
- Start date
- Apr 19, 2024
- End date
- Apr 25, 2025
- Enrollment
- 420 participants
Number of participants with Adverse Events (AEs)
The goal of this study is to assess and compare the safety and tolerability of salbutamol
 administered via metered dose inhaler (MDI) containing propellant 1,1-difluoroethane
 (HFA-152a) or 1,1,1,2-tetrafluoroethane (HFA-134a) in participants aged 12 years and above
 with asthma.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06261957
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06261957 through Pure Global AI's free database. This Phase 3 trial is sponsored by GlaxoSmithKline and is currently Not yet recruiting. The study focuses on Asthma. Target enrollment is 420 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.