Clinical Trials Directory

Trials / Completed

CompletedNCT00538694

Comparative Study of Cidecin™ (Daptomycin) to Rocephin® (Ceftriaxone) in the Treatment of Moderate to Severe Community-Acquired Acute Bacterial Pneumonia

A Randomized, Double-Blind, Phase III, Comparative Study of Cidecin™ (Daptomycin) to Rocephin® (Ceftriaxone) in the Treatment of Moderate to Severe Community-Acquired Acute Bacterial Pneumonia Due to S. Pneumoniae

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
Sponsor
Cubist Pharmaceuticals LLC, a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) · Industry
Sex
All
Age
18 Years
Healthy volunteers

Summary

To evaluate the safety and efficacy of daptomycin in adults who have pneumonia due to Streptococcus pneumoniae.

Conditions

Interventions

TypeNameDescription
DRUGdaptomycin

Timeline

Start date
2000-10-31
Primary completion
2001-09-30
Completion
2001-09-30
First posted
2007-10-03
Last updated
2019-11-14

Source: ClinicalTrials.gov record NCT00538694. Inclusion in this directory is not an endorsement.

Comparative Study of Cidecin™ (Daptomycin) to Rocephin® (Ceftriaxone) in the Treatment of Moderate to Severe Community-A (NCT00538694) · Clinical Trials Directory