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Study to Evaluate the Effect of FX006 on Synovial Inflammation in Patients With OA of the Knee
NCT03529942 · View on ClinicalTrials.gov ↗
Study Summary
This is an open-label study assessing the effect of the administration of a single intra-articular (IA) injection of FX006 32 mg on synovial volume in patients with osteoarthritis (OA) of the knee.
Conditions Studied
Interventions
- DRUG FX006 32 mg
Study Locations (10)
California
- TriWest Research Associates, LLC — El Cajon
- Biosolutions Research — La Mesa
- Dream Team Clinical Research (formerly located in Anaheim) — Pomona
- Dream Team Clinical Research — Pomona
Florida
- Tampa Bay Medical Research, Inc. — Clearwater
Illinois
- Rush University Medical Center — Chicago
North Carolina
- Duke University Medical Center — Durham
Pennsylvania
- Altoona Center for Clinical Research — Duncansville
Tennessee
- PMG Research, Inc. d/b/a PMG Research of Knoxville — Knoxville
Other
- University of Leeds — Leeds
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 129 participants |
| Start Date | 2018-04-24 |
| Est. Completion | 2020-03-09 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03529942
The ClinicalTrials.gov registry entry for NCT03529942 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 129 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pacira Pharmaceuticals, which has 31 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 Osteoarthritis, Knee appearing as the primary indexed condition, and to 1 intervention — of which FX006 32 mg 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: NCT03529942 reports 10 study locations spanning 7 distinct geographic areas — top geographies include California, Florida, Illinois. 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 NCT03529942 about?
NCT03529942 is a clinical study titled "Study to Evaluate the Effect of FX006 on Synovial Inflammation in Patients With OA of the Knee". This is an open-label study assessing the effect of the administration of a single intra-articular (IA) injection of FX006 32 mg on synovial volume in patients with osteoarthritis (OA) of the knee.
What is the current status of trial NCT03529942?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 129 participants. The study started on 2018-04-24. Estimated completion is 2020-03-09.
What conditions does trial NCT03529942 study?
This clinical trial studies the following conditions: Osteoarthritis, Knee. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03529942?
The interventions under investigation include: FX006 32 mg (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03529942?
This trial is sponsored by Pacira Pharmaceuticals, which has 31 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03529942 being conducted?
This trial has 10 study locations across California, Florida, Illinois, North Carolina, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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