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COMPLETED Phase 3

Efficacy and Safety Study of Guselkumab in the Treatment of Participants With Moderate to Severe Plaque-Type Psoriasis

NCT02905331 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of the study is to evaluate the efficacy, safety, pharmacokinetics, immunogenicity, usability, and acceptability of guselkumab delivered using SelfDose device in participants with moderate to severe plaque-type psoriasis.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG Guselkumab

Study Locations (14)

Other

  • Niepubliczny Zaklad Opieki Zdrowotnej Osteo-Medic s.c. Artur Racewicz i Jerzy Supronik — Bialystok
  • Szpital Uniwersytecki nr 1 im Dr A Jurasza — Bydgoszcz
  • Wromedica Irena Bielicka, Janusz Szczepanik S.C. — Wroclaw

Ontario

  • Dermatrials Research — Hamilton
  • DermEdge Research — Mississauga

Florida

  • Renstar Medical Research — Ocala

Illinois

  • Arlington Dermatology — Rolling Meadows

Indiana

  • Indiana Clinical Trial Center — Plainfield

Kentucky

  • Dermatology Specialists — Louisville

Michigan

  • Hamzavi Dermatology — Fort Gratiot

Pennsylvania

  • University of Pittsburgh Department of Dermatology — Pittsburgh

Trial Details

FieldValue
Enrollment Target 78 participants
Start Date 2017-02-28
Est. Completion 2018-02-06
Phase Phase 3

Sponsor

Janssen Research & Development

442 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02905331

The ClinicalTrials.gov registry entry for NCT02905331 describes a study currently listed as completed. It is categorized as Phase 3, 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 78 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Janssen Research & Development, which has 442 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 Psoriasis 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: NCT02905331 reports 14 study locations spanning 11 distinct geographic areas — top geographies include Other, Ontario, Florida. 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 NCT02905331 about?

NCT02905331 is a clinical study titled "Efficacy and Safety Study of Guselkumab in the Treatment of Participants With Moderate to Severe Plaque-Type Psoriasis". The purpose of the study is to evaluate the efficacy, safety, pharmacokinetics, immunogenicity, usability, and acceptability of guselkumab delivered using SelfDose device in participants with moderate to severe plaque-type psoriasis.

What is the current status of trial NCT02905331?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 78 participants. The study started on 2017-02-28. Estimated completion is 2018-02-06.

What conditions does trial NCT02905331 study?

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

What interventions are being tested in trial NCT02905331?

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

Who is sponsoring clinical trial NCT02905331?

This trial is sponsored by Janssen Research & Development, which has 442 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02905331 being conducted?

This trial has 14 study locations across Florida, Illinois, Indiana, Kentucky, 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