Trials / Completed
CompletedNCT00107978
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
- 1,035 (actual)
- Sponsor
- Cumberland Pharmaceuticals · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Study 0018 (NCT00107978) 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 administered every 12 hrs for up to 14 days. |
Timeline
- Start date
- 2005-02-01
- Primary completion
- 2006-05-01
- Completion
- 2006-05-01
- First posted
- 2005-04-12
- Last updated
- 2019-01-16
- Results posted
- 2010-02-01
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00107978. Inclusion in this directory is not an endorsement.