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Completed Phase 3 Interventional Results available

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 Oct 21, 2026, 1:55 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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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 \>=18 years with asthma

Study identification

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

Conditions and interventions

Conditions

Interventions

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 31, 2024 (Actual)
Primary completion
Sep 2, 2025 (Actual)
Completion
Sep 2, 2025 (Actual)
Last update posted
Oct 6, 2026

2024 – 2025

United States locations

U.S. sites
38
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 32789-3385 —
GSK Investigational Site Rincon Georgia 31326-5131 —
GSK Investigational Site Stonecrest Georgia 30038 —
GSK Investigational Site Louisville Kentucky 40217 —
GSK Investigational Site Owensboro Kentucky 42301 —
GSK Investigational Site Fall River Massachusetts 02723-1511 —
GSK Investigational Site Minneapolis Minnesota 55402-2508 —
GSK Investigational Site Minneota Minnesota 56001 —
GSK Investigational Site Olive Branch Mississippi 38654 —
GSK Investigational Site Columbia Missouri 65203 —
GSK Investigational Site Henderson Nevada 89052-5015 —
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 19464-3241 —
GSK Investigational Site Rock Hill South Carolina 29732 —
GSK Investigational Site Spartanburg South Carolina 29303-4225 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Union South Carolina 29379-7409 —
GSK Investigational Site Sugar Land Texas 77479 —
GSK Investigational Site Tomball Texas 77375-3332 —

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 Oct 6, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06261957 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →