drugset / Trial / NCT00446771

A Pharmacokinetic and Bioavailability Study of Mannitol for Inhalation Using Normal Subjects

NCT00446771

Phase 1 Completed 18 enrolled Syntara
RandomizedCrossoverOpen-labelTreatment

Summary

The study has an open-label, randomized, crossover design, in which each subject will receive mannitol powder for inhalation using a dry powder inhaler with and without premedication with a bronchodilator, mannitol powder for inhalation in capsules administered orally, and mannitol in a commercial formulation designed for intravenous use.

Timeline

Start
2006-10
Primary completion
Completion
2006-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Mannitol Diagnostic / imaging agent Inhaled

Indications

No indication recorded.