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A Study to Compare to the Pharmacokinetic Profile of Two Paracetamol Formulations
NCT01476189 · View on ClinicalTrials.gov ↗
Study Summary
A repeat dose pharmacokinetic study investigating two paracetamol formulations
Conditions Studied
Interventions
- DRUG Experimental paracetamol formulation
- DRUG Marketed paracetamol
- DRUG Higher dose marketed paracetamol
Study Locations (1)
Nebraska
- MDS Pharma Services NEBRASKA — Lincoln
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 28 participants |
| Start Date | 2009-11 |
| Est. Completion | 2009-12 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01476189
The ClinicalTrials.gov registry entry for NCT01476189 describes a study currently listed as completed. It is categorized as Phase 1, 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 28 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is GlaxoSmithKline, which has 558 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 Healthy Subjects appearing as the primary indexed condition, and to 3 interventions — of which Experimental paracetamol formulation 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: NCT01476189 reports 1 study location spanning 1 distinct geographic area — top geographies include Nebraska. 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 NCT01476189 about?
NCT01476189 is a clinical study titled "A Study to Compare to the Pharmacokinetic Profile of Two Paracetamol Formulations". A repeat dose pharmacokinetic study investigating two paracetamol formulations
What is the current status of trial NCT01476189?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 28 participants. The study started on 2009-11. Estimated completion is 2009-12.
What conditions does trial NCT01476189 study?
This clinical trial studies the following conditions: Healthy Subjects. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01476189?
The interventions under investigation include: Experimental paracetamol formulation (DRUG), Marketed paracetamol (DRUG), Higher dose marketed paracetamol (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01476189?
This trial is sponsored by GlaxoSmithKline, which has 558 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01476189 being conducted?
This trial has 1 study location across Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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