Clinical Trials Directory

Trials / Completed

CompletedNCT00097422

OPT-80 in Clostridium Difficile-Associated Diarrhea (CDAD)

An Open-Label, Dose Ranging, Randomized Clinical Evaluation of OPT-80 in Patients With Clostridium Difficile-Associated Diarrhea (CDAD)

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
Sponsor
Optimer Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to investigate the safety and perform preliminary clinical evaluation in patients with mild to moderate CDAD.

Detailed description

This is a dose-finding study to select a safe and efficacious dose of OPT-80. Patients will be evaluated for safety and efficacy and pharmacokinetic parameters will be investigated.

Conditions

Interventions

TypeNameDescription
DRUGOPT-80

Timeline

Start date
2004-11-01
Primary completion
2005-04-01
Completion
2005-04-01
First posted
2004-11-24
Last updated
2017-03-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00097422. Inclusion in this directory is not an endorsement.

OPT-80 in Clostridium Difficile-Associated Diarrhea (CDAD) (NCT00097422) · Clinical Trials Directory