Pharmacokinetic Study Investigating the Extent of Paracetamol Absorption From a New Formulation of Paracetamol Compared With Panadol® Extend
Completed · Phase 1
Conditions studied: Healthy Subjects
In brief
This study will evaluate the pharmacokinetic profiles of experimental formulations of paracetamol.
Key facts
- Study ID
- NCT01540721
- Run by
- GlaxoSmithKline
- People needed
- 28
- Starts
- 2009-12-01
- Expected to finish
- 2009-12-01
- Last updated by the study team
- 2014-11-24
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Good health with (in the opinion of the investigator) no clinically significant and relevant abnormalities of medical history or physical examination
You may not qualify if…
- Current (within 14 days of screening) or regular use of any prescription, over the counter (OTC) drugs including paracetamol/acetaminophen, herbal medicine or drug known to induce or inhibit hepatic drug metabolism, excluding prescription birth control, if applicable.
Where it is running
- MDS Pharma Services NEBRASKA — Lincoln, Nebraska, United States
Full record on ClinicalTrials.gov
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