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Active, not recruiting Phase 2 Interventional

A Dose Finding Study With an Anti-TSLP Antibody (GSK5784283) in Adults Aged 18 to 75 Years of Age With Uncontrolled Asthma

ClinicalTrials.gov ID: NCT06748053

Public ClinicalTrials.gov record NCT06748053. 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 22, 2026, 4:20 PM 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 Multicentre, Randomized, Double-Blind, Placebo Controlled, Dose Finding, Parallel Group, Phase 2 Study of an Anti-TSLP Antibody (GSK5784283) in Adults Aged 18 to 75 Years of Age With Uncontrolled Asthma

Brief summary

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

This study is trying to find the right dose of a long-lasting medicine called GSK5784283 for people with asthma that remains uncontrolled even though they are using regular asthma treatments. GSK5784283 blocks the action of an inflammatory protein called TSLP that may be contributing to your asthma. The study will be conducted in two parts - Part A (dose finding phase) and Part B (extended dosing phase). Part A will assess the lung function, asthma control, participant safety and certain markers of asthma inflammation in the air you breath out and in your blood. Part B will assess the safety and long-term effects of the repeated or single doses of GSK5784283.

Study identification

NCT ID
NCT06748053
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
307 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Feb 10, 2025 (Actual)
Primary completion
Jul 14, 2026 (Actual)
Completion
Sep 9, 2027 (Estimated)
Last update posted
Aug 12, 2026

2025 – 2027

United States locations

U.S. sites
51
U.S. states
19
U.S. cities
47
Facility City State ZIP Site status
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Long Beach California 90815 —
GSK Investigational Site Los Angeles California 90025 —
GSK Investigational Site Redding California 96001 —
GSK Investigational Site Riverside California 92506 —
GSK Investigational Site Sacramento California 95817 —
GSK Investigational Site San Jose California 95117 —
GSK Investigational Site Colorado Springs Colorado 80923 —
GSK Investigational Site Lakewood Colorado 80228-1813 —
GSK Investigational Site Wheat Ridge Colorado 80033 —
GSK Investigational Site New Haven Connecticut 06511 —
GSK Investigational Site Aventura Florida 33180 —
GSK Investigational Site Hialeah Florida 33012 —
GSK Investigational Site Lake Worth Florida 33460 —
GSK Investigational Site Leesburg Florida 34748 —
GSK Investigational Site Miami Florida 33144 —
GSK Investigational Site Miami Florida 33166 —
GSK Investigational Site Miami Florida 33172 —
GSK Investigational Site Miami Florida 33173 —
GSK Investigational Site Plantation Florida 33324 —
GSK Investigational Site Tampa Florida 33607 —
GSK Investigational Site Skokie Illinois 60077 —
GSK Investigational Site Shreveport Louisiana 71105 —
GSK Investigational Site Lathrup Village Michigan 48076 —
GSK Investigational Site Warren Michigan 48088 —
GSK Investigational Site St Louis Missouri 63119 —
GSK Investigational Site Omaha Nebraska 68198 —
GSK Investigational Site The Bronx New York 10461 —
GSK Investigational Site Cincinnati Ohio 45236 —
GSK Investigational Site DuBois Pennsylvania 15801 —
GSK Investigational Site Philadelphia Pennsylvania 19140 —
GSK Investigational Site Pittsburgh Pennsylvania 15241 —
GSK Investigational Site Wyomissing Pennsylvania 19610 —
GSK Investigational Site Warwick Rhode Island 02886 —
GSK Investigational Site Greenville South Carolina 29607 —
GSK Investigational Site Spartanburg South Carolina 29303 —
GSK Investigational Site Knoxville Tennessee 37909 —
GSK Investigational Site Boerne Texas 78006 —
GSK Investigational Site Cypress Texas 77429 —
GSK Investigational Site Dallas Texas 75225 —
GSK Investigational Site Houston Texas 77058 —
GSK Investigational Site Kerrville Texas 78028 —
GSK Investigational Site McKinney Texas 75069 —
GSK Investigational Site San Antonio Texas 78212 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site Sherman Texas 75092 —
GSK Investigational Site American Fork Utah 84003 —
GSK Investigational Site Pleasant View Utah 84404 —
GSK Investigational Site Salt Lake City Utah 84117 —
GSK Investigational Site South Ogden Utah 84405 —
GSK Investigational Site Bellingham Washington 98225 —

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 83 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06748053, 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 Aug 12, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06748053 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →