Trial intelligence / Profile preview

Optimal duration of moxifloxacin therapy in uncomplicated acute cholangitis

2005-004851-37Phase 3Terminated

Sponsor
Regensburg University Medical Center
Start
Dec 2007
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Countries
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Overview

Phase 3, randomised, double-blind trial in acute cholangitis and cholangiolitis comparing Oral Avalox continuation with Oral placebo continuation (2 arms). Primary endpoint: Combined rate of relapse, complications, and death within 28 days. Started Dec 2007; status: terminated.

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Drugs

moxifloxacin
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Conditions

acute cholangitischolangiolitis

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