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Phase II Study to Evaluate Efficacy and Safety of D-0120 in Combination With Allopurinol in Subjects With Gout
NCT05665699 · View on ClinicalTrials.gov ↗
Study Summary
D-0120 is being tested in combination with Allopurinol in adult subjects with Gout.
Conditions Studied
Interventions
- DRUG Allopurinol
- DRUG D-0120
Study Locations (19)
North Carolina
- Study Center — Hickory
- Study Center — Rocky Mount
- Study Center — Salisbury
- Study Center — Wilmington
- Study Center — Winston-Salem
Tennessee
- Study Center — Bristol
- Site Center — Hendersonville
- Study Center — Knoxville
Texas
- Site Center — Fort Worth
- Site Center — The Woodlands
Alabama
- Study Center — Birmingham
Florida
- Site Center — Plantation
Illinois
- Study Center — Evergreen Park
Indiana
- Study Center — Brownsburg
Kentucky
- Site Center — Louisville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2023-04-17 |
| Est. Completion | 2025-12-30 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05665699
The ClinicalTrials.gov registry entry for NCT05665699 describes a study currently listed as active not recruiting. 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 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is InventisBio Co., which has 32 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 Gout appearing as the primary indexed condition, and to 2 interventions — of which Allopurinol 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: NCT05665699 reports 19 study locations spanning 12 distinct geographic areas — top geographies include North Carolina, Tennessee, Texas. 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 NCT05665699 about?
NCT05665699 is a clinical study titled "Phase II Study to Evaluate Efficacy and Safety of D-0120 in Combination With Allopurinol in Subjects With Gout". D-0120 is being tested in combination with Allopurinol in adult subjects with Gout.
What is the current status of trial NCT05665699?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 80 participants. The study started on 2023-04-17. Estimated completion is 2025-12-30.
What conditions does trial NCT05665699 study?
This clinical trial studies the following conditions: Gout. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05665699?
The interventions under investigation include: Allopurinol (DRUG), D-0120 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05665699?
This trial is sponsored by InventisBio Co., which has 32 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05665699 being conducted?
This trial has 19 study locations across Alabama, Florida, Illinois, Indiana, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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