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COMPLETED Phase 2

To Assess the Safety and Activity of GBR 830, Compared to Placebo, in Adults With Moderate-to-severe Atopic Dermatitis

NCT02683928 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine the effect of GBR 830 on biomarkers in atopic dermatitis to enable further studies in this indication.

Conditions Studied

Interventions

  • BIOLOGICAL Placebo
  • BIOLOGICAL GBR 830

Study Locations (17)

Ontario

  • Glenmark Investigational Site 8 — Markham
  • Glenmark Investigational Site 7 — Peterborough
  • Glenmark Investigational Site 6 — Richmond Hill
  • Glenmark Investigational Site 10 — Waterloo

Texas

  • Glenmark Investigational Site 2 — Dallas
  • Glenmark Investigational Site 17 — Katy
  • Glenmark Investigational Site 12 — Webster

California

  • Glenmark Investigational Site 5 — Los Angeles
  • Glenmark Investigational Site 3 — San Diego

Arkansas

  • Glenmark Investigational Site 14 — Rogers

Florida

  • Glenmark Investigational Site 15 — Tampa

Missouri

  • Glenmark Investigational Site 11 — St Louis

New Jersey

  • Glenmark Investigational Site 16 — Berlin

New York

  • Glenmark Investigational Site 1 — New York

Trial Details

FieldValue
Enrollment Target 64 participants
Start Date 2016-03
Est. Completion 2017-06
Phase Phase 2

Sponsor

Ichnos Sciences

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02683928

The ClinicalTrials.gov registry entry for NCT02683928 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 64 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ichnos Sciences, which has 2 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 Atopic Dermatitis 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: NCT02683928 reports 17 study locations spanning 11 distinct geographic areas — top geographies include Ontario, Texas, California. 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 NCT02683928 about?

NCT02683928 is a clinical study titled "To Assess the Safety and Activity of GBR 830, Compared to Placebo, in Adults With Moderate-to-severe Atopic Dermatitis". The purpose of this study is to determine the effect of GBR 830 on biomarkers in atopic dermatitis to enable further studies in this indication.

What is the current status of trial NCT02683928?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 64 participants. The study started on 2016-03. Estimated completion is 2017-06.

What conditions does trial NCT02683928 study?

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

What interventions are being tested in trial NCT02683928?

The interventions under investigation include: Placebo (BIOLOGICAL), GBR 830 (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02683928?

This trial is sponsored by Ichnos Sciences, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02683928 being conducted?

This trial has 17 study locations across Arkansas, California, Florida, Missouri, New Jersey. 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