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COMPLETED Phase 2

A Study to Test the Ability of and Safety of GSK2110183 in Treating Langerhans Cell Histiocytosis

NCT01395004 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study was to assess safety and efficacy at months 3 and 6 in patients with Langerhans Cell Histiocytosis given daily oral doses of GSK2110183.

Interventions

  • DRUG GSK2110183

Study Locations (5)

New York

  • Memorial Sloan Kettering Cancer Center — New York
  • Staten Island University Hospital — Staten Island

Maryland

  • Johns Hopkins Hospital — Baltimore

Massachusetts

  • Dana Farber Cancer Institute — Boston

Texas

  • Baylor College of Medicine — Houston

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2011-11
Est. Completion 2013-11
Phase Phase 2

Sponsor

GlaxoSmithKline

558 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01395004

The ClinicalTrials.gov registry entry for NCT01395004 describes a study currently listed as completed. It is categorized as Phase 2, 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 17 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 Langerhans Cell Histiocytosis appearing as the primary indexed condition, and to 1 intervention — of which GSK2110183 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: NCT01395004 reports 5 study locations spanning 4 distinct geographic areas — top geographies include New York, Maryland, Massachusetts. 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 NCT01395004 about?

NCT01395004 is a clinical study titled "A Study to Test the Ability of and Safety of GSK2110183 in Treating Langerhans Cell Histiocytosis". The purpose of this study was to assess safety and efficacy at months 3 and 6 in patients with Langerhans Cell Histiocytosis given daily oral doses of GSK2110183.

What is the current status of trial NCT01395004?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 17 participants. The study started on 2011-11. Estimated completion is 2013-11.

What conditions does trial NCT01395004 study?

This clinical trial studies the following conditions: Langerhans Cell Histiocytosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01395004?

The interventions under investigation include: GSK2110183 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01395004?

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 NCT01395004 being conducted?

This trial has 5 study locations across Maryland, Massachusetts, New York, Texas. 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