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Terminated Phase 2 Interventional Results available

A Dose-Finding Study to Evaluate the Efficacy and Safety of GSK3858279 in Adults With Knee Osteoarthritis (OA) Pain

ClinicalTrials.gov ID: NCT05838742

Public ClinicalTrials.gov record NCT05838742. 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 May 17, 2026, 5:00 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 Multicentre Randomized, Double-blind, Placebo Controlled, Dose-finding, Phase 2 Study (MARS-17) of GSK3858279 in Adult Participants With Moderate to Severe Pain Due to Knee Osteoarthritis

Study identification

NCT ID
NCT05838742
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
314 participants

Conditions and interventions

Interventions

  • GSK3858279 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
40 Years to 80 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
Sep 12, 2023
Primary completion
Aug 11, 2024
Completion
Dec 2, 2024
Last update posted
Nov 9, 2025

2023 – 2024

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
14
Facility City State ZIP Site status
GSK Investigational Site Cerritos California 90703
GSK Investigational Site Huntington Beach California 92647
GSK Investigational Site Santa Clara California 95054
GSK Investigational Site Cooper City Florida 33024
GSK Investigational Site Cutler Bay Florida 33189
GSK Investigational Site Miami Florida 33173
GSK Investigational Site Miami Florida 33185
GSK Investigational Site Wichita Kansas 67207
GSK Investigational Site Louisville Kentucky 40213
GSK Investigational Site New Orleans Louisiana 70115
GSK Investigational Site Henderson Nevada 89052
GSK Investigational Site Williamsville New York 14221
GSK Investigational Site Greensboro North Carolina 27410
GSK Investigational Site Duncansville Pennsylvania 16635
GSK Investigational Site Charlottesville Virginia 22911

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 78 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05838742, 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 Nov 9, 2025 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05838742 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →