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NCT05838742 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by GlaxoSmithKline.

Terminated
Registry status
Phase 2
Development phase
314
Enrollment target

NCT05838742: Clinical Trial Phase 2 study, sponsored by GlaxoSmithKline.

NCT05838742 is a Phase 2 study that was terminated before completion, run by GlaxoSmithKline. The registered enrollment target is 314 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (136% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05838742, a Phase 2 study, was terminated before completion, sponsored by GlaxoSmithKline.

TERMINATED
Registry status
Phase 2
Development phase
314 participants
Enrollment target

Study Summary

This is dose-finding study of GSK3858279 in participants with moderate to severe knee osteoarthritis pain. The purpose of this study is to investigate and provide the data necessary to select the optimal effective and safe dose(s) of GSK3858279.

Primary Outcome

Change from Baseline in knee pain due to Osteoarthritis were reported by weekly average of average daily pain numeric rating scale (NRS) at Week 12. The pain NRS is an 11-point scale (ranging from 0-10) for self-reporting of average daily knee pain where 0 indicates no pain, and 10 indicates the worst possible pain. For each participant, the weekly average of average daily pain score was calculated using the mean value of available daily pain scores falling in the assessment window for each week

Interventions

  • DRUG Placebo
  • DRUG GSK3858279

Trial Details

FieldValue
Enrollment Target 314 participants
Start Date 2023-09-13
Est. Completion 2024-12-03
Phase Phase 2
GlaxoSmithKline

1,345 total trials

Why NCT05838742 stopped before completion

NCT05838742 is an interventional study that assigns participants to a tested intervention. The registered 314 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (136% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT05838742 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05838742 about?

NCT05838742 is a clinical study titled "A Dose-Finding Study to Evaluate the Efficacy and Safety of GSK3858279 in Adults With Knee Osteoarthritis (OA) Pain". This is dose-finding study of GSK3858279 in participants with moderate to severe knee osteoarthritis pain. The purpose of this study is to investigate and provide the data necessary to select the optimal effective and safe dose(s) of GSK3858279.

What is the current status of trial NCT05838742?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 314 participants. The study started on 2023-09-13. Estimated completion is 2024-12-03.

What interventions are being tested in trial NCT05838742?

The interventions under investigation include: Placebo (DRUG), GSK3858279 (DRUG).

Who is sponsoring clinical trial NCT05838742?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05838742's enrollment target sits among peer trials

314 159th of 2000 higher than 1,840 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05838742, the US trial registry maintained by the National Library of Medicine. NCT05838742 (mid enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.