Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING Phase 1

A Study for GSK3862995B in Healthy Participants and Participants With Chronic Obstructive Pulmonary Disease

NCT06154837 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of the study is to investigate the safety and tolerability of ascending doses of GSK3862995B following single dose in healthy participants and repeat doses in participants with Chronic obstructive pulmonary disease (COPD).

Interventions

  • DRUG Placebo
  • DRUG GSK3862995B

Study Locations (20)

Other

  • GSK Investigational Site — Ahrensburg
  • GSK Investigational Site — Berlin
  • GSK Investigational Site — Berlin
  • GSK Investigational Site — Berlin
  • GSK Investigational Site — Dresden
  • GSK Investigational Site — Frankfurt
  • GSK Investigational Site — Hamburg
  • GSK Investigational Site — Hamburg
  • GSK Investigational Site — Hanover
  • GSK Investigational Site — Immenhausen
  • GSK Investigational Site — Leipzig

Florida

  • GSK Investigational Site — Hialeah
  • GSK Investigational Site — Plantation

North Carolina

  • GSK Investigational Site — Shelby
  • GSK Investigational Site — Wilmington

Arizona

  • GSK Investigational Site — Yuma

Georgia

  • GSK Investigational Site — Columbus

Oregon

  • GSK Investigational Site — Medford

South Carolina

  • GSK Investigational Site — Rock Hill

Texas

  • GSK Investigational Site — Austin

Trial Details

FieldValue
Enrollment Target 130 participants
Start Date 2023-11-27
Est. Completion 2027-03-31
Phase Phase 1

Sponsor

GlaxoSmithKline

558 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06154837

The ClinicalTrials.gov registry entry for NCT06154837 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 130 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is GlaxoSmithKline, which has 558 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Pulmonary Disease, Chronic Obstructive appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06154837 reports 20 study locations spanning 8 distinct geographic areas — top geographies include Other, Florida, North Carolina. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06154837 about?

NCT06154837 is a clinical study titled "A Study for GSK3862995B in Healthy Participants and Participants With Chronic Obstructive Pulmonary Disease". The primary objective of the study is to investigate the safety and tolerability of ascending doses of GSK3862995B following single dose in healthy participants and repeat doses in participants with Chronic obstructive pulmonary disease (COPD).

What is the current status of trial NCT06154837?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 130 participants. The study started on 2023-11-27. Estimated completion is 2027-03-31.

What conditions does trial NCT06154837 study?

This clinical trial studies the following conditions: Pulmonary Disease, Chronic Obstructive. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06154837?

The interventions under investigation include: Placebo (DRUG), GSK3862995B (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06154837?

This trial is sponsored by GlaxoSmithKline, which has 558 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06154837 being conducted?

This trial has 20 study locations across Arizona, Florida, Georgia, North Carolina, Oregon. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial