Trials / Completed
CompletedNCT00091819
Comparison of Telavancin and Vancomycin for Complicated Skin and Skin Structure Infections With a Focus on Methicillin-resistant Staphylococcus Aureus
A Phase 3, Randomized, Double Blind, Multinational Trial of Intravenous Telavancin Versus Vancomycin for Treatment of Complicated Gram Positive Skin and Skin Structure Infections With a Focus on Patients With Infections Due to Methicillin-resistant Staphylococcus Aureus
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 862 (actual)
- Sponsor
- Cumberland Pharmaceuticals · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Study 0017 compares the safety and effectiveness of an investigational drug, telavancin, and an approved drug, vancomycin, for the treatment of complicated skin and skin structure infections.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Telavancin | Telavancin 10 mg/kg/day, IV for up to 14 days. |
| DRUG | Vancomycin | Vancomycin 1 Gm IV q 12 hrs for up to 14 days. |
Timeline
- Start date
- 2005-01-01
- Primary completion
- 2006-06-01
- Completion
- 2006-06-01
- First posted
- 2004-09-21
- Last updated
- 2019-01-16
- Results posted
- 2009-12-08
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00091819. Inclusion in this directory is not an endorsement.