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COMPLETED Phase 2

Proof of Concept Study of Gevokizumab in the Treatment of Pyoderma Gangrenosum

NCT01882504 · View on ClinicalTrials.gov ↗

Study Summary

The study will evaluate the safety and biologic activity of gevokizumab in subjects in the acute inflammatory phase of pyoderma gangrenosum.

Conditions Studied

Interventions

  • DRUG gevokizumab

Study Locations (19)

Texas

  • — Arlington
  • — Dallas
  • — Houston

Florida

  • — Miami
  • — Miami Shores

Ohio

  • — Cleveland
  • — Columbus

Alabama

  • — Birmingham

Illinois

  • — Chicago

Maryland

  • — Baltimore

Michigan

  • — Ann Arbor

Minnesota

  • — Minneapolis

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2013-05
Est. Completion 2015-10
Phase Phase 2

Sponsor

XOMA (US)

4 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01882504

The ClinicalTrials.gov registry entry for NCT01882504 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 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is XOMA (US), which has 4 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 Pyoderma Gangrenosum appearing as the primary indexed condition, and to 1 intervention — of which gevokizumab 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: NCT01882504 reports 19 study locations spanning 15 distinct geographic areas — top geographies include Texas, Florida, Ohio. 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 NCT01882504 about?

NCT01882504 is a clinical study titled "Proof of Concept Study of Gevokizumab in the Treatment of Pyoderma Gangrenosum". The study will evaluate the safety and biologic activity of gevokizumab in subjects in the acute inflammatory phase of pyoderma gangrenosum.

What is the current status of trial NCT01882504?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 8 participants. The study started on 2013-05. Estimated completion is 2015-10.

What conditions does trial NCT01882504 study?

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

What interventions are being tested in trial NCT01882504?

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

Who is sponsoring clinical trial NCT01882504?

This trial is sponsored by XOMA (US), which has 4 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01882504 being conducted?

This trial has 19 study locations across Alabama, Florida, Illinois, Maryland, Michigan. 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