drugset / Trial / NCT00464802

Study Evaluating the Safety and Tolerability of a New Intravenous Formulation of MOA-728 in Healthy Subjects

NCT00464802

Phase 1 Completed 36 enrolled Bausch Health Americas, Inc.
RandomizedCrossoverDouble-blindTreatment

Summary

The primary objective is to determine the safety and tolerability of the new IV formulation versus the current formulation of MOA-728 focusing on the theoretical potential for infusion-related and formulation-related complications.

Timeline

Start
2007-04
Primary completion
Completion
2007-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Methylnaltrexone Other / unclassified Intravenous

Indications

No indication recorded.