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A Study to Compare to the Pharmacokinetic Profile of Two Paracetamol Formulations

NCT01476189 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2014-11-24

No results posted yet for this study

Summary

A repeat dose pharmacokinetic study investigating two paracetamol formulations

Conditions

  • Healthy Subjects

Interventions

DRUG

Experimental paracetamol formulation

experimental

DRUG

Marketed paracetamol

Marketed paracetamol

DRUG

Higher dose marketed paracetamol

Higher dose marketed paracetamol

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2009-12-31
Completion
2009-12-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01476189 on ClinicalTrials.gov