Clinical Trials Directory

Trials / Completed

CompletedNCT00994942

Bioequivalency Study of Morphine Sulfate Injection, Solution and Tablet Under Fasted Conditions

A Single Dose, Three-Period, Three-Treatment, Six-Sequence, Three-Way Crossover Pharmacokinetic and Comparative Bioavailability Study of Morphine Sulfate Injection, Solution, and Tablet Formulations Under Fasting Conditions.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
18 (actual)
Sponsor
Roxane Laboratories · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Determine the pharmacokinetics and optimize study design for subsequent studies with morphine sulfate tablets and solution.

Conditions

Interventions

TypeNameDescription
DRUGmorphine sulfatemorphine sulfate 30 mg tablet, morphine sulfate 30 mg (10 mg / 5 mL) oral solution, morphine sulfate injection 10 mg (1 mg / mL)

Timeline

Start date
2006-04-01
Primary completion
2006-04-01
Completion
2006-04-01
First posted
2009-10-14
Last updated
2018-01-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00994942. Inclusion in this directory is not an endorsement.

Bioequivalency Study of Morphine Sulfate Injection, Solution and Tablet Under Fasted Conditions (NCT00994942) · Clinical Trials Directory