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A Study to Evaluate the Efficacy and Safety of INCB054707 in Participants With Prurigo Nodularis
NCT05061693 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of this study is to evaluate the efficacy and safety of INCB054707 in participants with prurigo nodularis over a 16-week double-blind placebo-controlled treatment period, followed by a 24 -week single blind extension period.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG INCB054707
Study Locations (20)
Florida
- Investigative Site US019 — Fort Lauderdale
- Investigative Site US016 — Miami
- Investigative Site US013 — Miramar
- Investigative Site US009 — Tampa
Ohio
- Investigative Site US023 — Athens
- Investigative Site US002 — Dublin
- Investigative Site US012 — Gahanna
Arizona
- Investigative Site US010 — Phoenix
- Investigative Site US024 — Phoenix
California
- Investigative Site US001 — Fountain Valley
- Investigative Site US014 — Sacramento
Indiana
- Investigative Site US008 — Plainfield
- Investigative Site US011 — South Bend
Georgia
- Investigative Site 1071320 — Newnan
Maryland
- Investigative Site US003 — Baltimore
Michigan
- Investigative Site US017 — Troy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 146 participants |
| Start Date | 2021-11-04 |
| Est. Completion | 2024-02-28 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05061693
The ClinicalTrials.gov registry entry for NCT05061693 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 146 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Incyte Corporation, which has 163 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 Prurigo Nodularis 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: NCT05061693 reports 20 study locations spanning 12 distinct geographic areas — top geographies include Florida, Ohio, Arizona. 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 NCT05061693 about?
NCT05061693 is a clinical study titled "A Study to Evaluate the Efficacy and Safety of INCB054707 in Participants With Prurigo Nodularis". The purpose of this study is to evaluate the efficacy and safety of INCB054707 in participants with prurigo nodularis over a 16-week double-blind placebo-controlled treatment period, followed by a 24 -week single blind extension period.
What is the current status of trial NCT05061693?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 146 participants. The study started on 2021-11-04. Estimated completion is 2024-02-28.
What conditions does trial NCT05061693 study?
This clinical trial studies the following conditions: Prurigo Nodularis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05061693?
The interventions under investigation include: Placebo (DRUG), INCB054707 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05061693?
This trial is sponsored by Incyte Corporation, which has 163 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05061693 being conducted?
This trial has 20 study locations across Arizona, California, Florida, Georgia, Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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