drugset / Trial / NCT01595867

Abuse Potential Assessment of Intranasally Administered EMBEDA Compared To Morphine Sulfate Controlled Release And Placebo

NCT01595867

Phase 1 Completed 33 enrolled Pfizer
RandomizedCrossoverDouble-blindBasic science

Summary

This was a single-dose, randomized, double-blind, placebo-controlled, 3 way crossover study designed to evaluate the relative abuse potential of crushed EMBEDA® compared to morphine sulfate CR tablets and placebo in healthy male and female, non-dependent, recreational opioid users. An appropriate dose of morphine sulfate CR (i.e., 30 mg, 60 or 90 mg) was to be selected during Part A of the study (Dose Selection Phase). Each subject participated in the study for up to (approximately) 16 weeks and was confined in the clinic for a total of up to 12 nights.

Timeline

Start
2010-08
Primary completion
2011-01
Completion
2011-01

Drugs

EvaluationDrugModalityDoseRoute
Subject EMBEDA Unknown 1.2 mg Intranasal
Subject EMBEDA Unknown 30 mg Intranasal
Comparator Morphine Other / unclassified 30 mg Intranasal