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Terminated Phase 2 Interventional Results available

A Study to Evaluate Efficacy and Safety of GSK3858279 in Diabetic Peripheral Neuropathic Pain

ClinicalTrials.gov ID: NCT05838755

Public ClinicalTrials.gov record NCT05838755. 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 Jun 26, 2026, 6:23 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 Multicenter Randomized, Double-blind, Placebo-controlled Phase 2 Study to Evaluate Efficacy, Safety, Tolerability, Pharmacokinetics and Target Engagement of GSK3858279 in Adult Participants With Chronic Diabetic Peripheral Neuropathic Pain (DPNP) /NEPTUNE-17

Study identification

NCT ID
NCT05838755
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
147 participants

Conditions and interventions

Conditions

Interventions

  • GSK3858279 Drug
  • Placebo Drug

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
Sep 19, 2023
Primary completion
Oct 13, 2024
Completion
Feb 16, 2025
Last update posted
Nov 20, 2025

2023 – 2025

United States locations

U.S. sites
19
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
GSK Investigational Site Anniston Alabama 36207
GSK Investigational Site Surprise Arizona 85378
GSK Investigational Site Cerritos California 90703
GSK Investigational Site Lomita California 90717
GSK Investigational Site Largo Florida 33777
GSK Investigational Site Miami Florida 33135
GSK Investigational Site Miami Florida 33175
GSK Investigational Site West Palm Beach Florida 33401
GSK Investigational Site Decatur Georgia 30030
GSK Investigational Site Chicago Illinois 60611
GSK Investigational Site Waltham Massachusetts 02451
GSK Investigational Site Williamsville New York 14221
GSK Investigational Site Huntersville North Carolina 28078
GSK Investigational Site Lancaster South Carolina 29720
GSK Investigational Site Cypress Texas 77429
GSK Investigational Site DeSoto Texas 75154
GSK Investigational Site Houston Texas 77030
GSK Investigational Site McAllen Texas 78501
GSK Investigational Site Bellevue Washington 98007

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 62 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05838755, 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 20, 2025 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05838755 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →