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Completed Phase 3 Interventional

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 ≥ 18 Years of Age With Asthma

ClinicalTrials.gov ID: NCT06261957

Public ClinicalTrials.gov record NCT06261957. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 22, 2026, 4:24 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized, Double-blind, Parallel Group, Multi-center Study to Evaluate the Long-term Safety of Salbutamol Rescue Medication When Administered Via Metered Dose Inhalers Containing the Propellant HFA-152a or Reference HFA-134a

Study identification

NCT ID
NCT06261957
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
477 participants

Conditions and interventions

Conditions

Interventions

  • Salbutamol HFA-134a Drug
  • Salbutamol HFA-152a Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 30, 2024
Primary completion
Sep 1, 2025
Completion
Sep 1, 2025
Last update posted
Feb 26, 2026

2024 – 2025

United States locations

U.S. sites
37
U.S. states
17
U.S. cities
35
Facility City State ZIP Site status
GSK Investigational Site North Hollywood California 91606-3287
GSK Investigational Site San Mateo California 94403
GSK Investigational Site Aventura Florida 33180
GSK Investigational Site Clearwater Florida 33756
GSK Investigational Site DeLand Florida 32720
GSK Investigational Site Miami Florida 33144
GSK Investigational Site Miami Florida 33155
GSK Investigational Site Miami Florida 33173
GSK Investigational Site Naples Florida 34102
GSK Investigational Site Plantation Florida 33317
GSK Investigational Site Winter Park Florida 32789
GSK Investigational Site Rincon Georgia 31326
GSK Investigational Site Stonecrest Georgia 30038
GSK Investigational Site Louisville Kentucky 40217
GSK Investigational Site Owensboro Kentucky 42301
GSK Investigational Site Fall River Massachusetts 02723
GSK Investigational Site Minneapolis Minnesota 55402
GSK Investigational Site Minneota Minnesota 56001
GSK Investigational Site Olive Branch Mississippi 38654
GSK Investigational Site Columbia Missouri 65203
GSK Investigational Site Henderson Nevada 89052
GSK Investigational Site Jersey City New Jersey 07306
GSK Investigational Site Riverdale New Jersey 07457
GSK Investigational Site Brooklyn New York 11220
GSK Investigational Site Asheville North Carolina 28803
GSK Investigational Site Winston-Salem North Carolina 27104
GSK Investigational Site Cincinnati Ohio 45231
GSK Investigational Site Dublin Ohio 43016
GSK Investigational Site Medford Oregon 97504
GSK Investigational Site Philadelphia Pennsylvania 19107
GSK Investigational Site Pittsburgh Pennsylvania 15241
GSK Investigational Site Pottstown Pennsylvania 19464
GSK Investigational Site Rock Hill South Carolina 29732
GSK Investigational Site Spartanburg South Carolina 29303
GSK Investigational Site Union South Carolina 29379
GSK Investigational Site Sugar Land Texas 77479
GSK Investigational Site Tomball Texas 77375

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 64 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06261957, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 26, 2026 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT06261957 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →