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A phase 3, randomized, double-blind study of ceftobiprole versus vancomycin in the treatment of complicated skin and skin structure infections

Conditions
Suspected or proven complicated skin and soft tissues infections, caused by staphilococcus metcillin resistant species (MRSS), Metcillin Staphilococcus Aureus Resistant (MTSA) included.
MedDRA version: 6.1Level: HLGTClassification code 10040792
Registration Number
EUCTR2004-001662-41-IT
Lead Sponsor
BASILEA PHARMACEUTICA
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
700
Inclusion Criteria

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: ;Secondary Objective: ;Primary end point(s):
Secondary Outcome Measures
NameTimeMethod
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