CompletedPhase 3ACTRN12605000324617

A Phase 3, Randomized, Double-Blind, Parallel-Group, Multinational Trial of Intravenous Telavancin Versus Vancomycin for Treatment of Hospital-Acquired Pneumonia with a Focus on Patients with Infections Due to Methicillin-Resistant Staphylococcus aureus (ATTAIN I & ATTAIN II)


Sponsor

Theravance, Inc.

Enrollment

750 participants

Start Date

Feb 1, 2005

Study Type

Interventional

Conditions


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

This is a phase 3, randomized, double-blind, parallel-group, multinational trial of intravenous telavancin versus vancomycin for treatment of hospital-acquired pneumonia with a focus on patients with infections due to methicillin-resistant staphylococcus aureus (attain i & attain ii). It may be open to people who are at least 18 years old. Participants generally need to have diagnosis of hospital acquired pneumonia.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

Telavancin 10 mg/kg q 24 hours IV

Telavancin 10 mg/kg q 24 hours IV


Locations(1)

United States of America

View Full Details on ANZCTR

For the most up-to-date information, visit the official listing.

Visit

ACTRN12605000324617