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Pharmacokinetic (PK) Study of OxyNorm Injections in Chinese Patient

Pain Clinical Trial

Official title:
A Single Dose PK Study of Oxycodone Hydrochloride Injection 2.5, 5, and 10mg in Chinese Patients With Cancer Pain or Post-operation Patients

Clinical Trial Summary

This is a single center, open label, randomized, parallel group single dose intravenous (i.v.) administration study. The subjects will be randomized to receive a single dose of OxyNorm® 2.5, 5, and 10mg.

Clinical Trial Description

After up to 7 days screening period, Eligible Patients will be randomized to 1 of 3 groups, and begin treatment with single dose of OxyNorm® 2.5,5, and 10mg. ;

Study Design

Endpoint Classification: Pharmacokinetics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01482936
Study type Interventional
Source Mundipharma (China) Pharmaceutical Co. Ltd
Contact
Status Completed
Phase Phase 1
Start date May 2010
View Details
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