drugset / Trial / NCT00686335

A New Modified-release Tablet Formulation of Prednisone (Lodotra®) in Patients With Nocturnal Asthma

NCT00686335 ↗

Phase 2 Completed 12 enrolled Amgen
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to evaluate in subjects suffering from nocturnal asthma, the efficacy and safety of modified release Prednisone on signs and symptoms.

Timeline

Start
2008-06
Primary completion
2010-03
Completion
2010-05

Drugs

EvaluationDrugModalityDoseRoute
Comparator Prednisone Other / unclassified 1 mg —
Comparator Prednisone Other / unclassified 5 mg —
Comparator Prednisone Other / unclassified 1 mg —
Comparator Prednisone Other / unclassified 5 mg —

Indications