A Phase IIb, 96 week, randomized, open-label, multicenter,parallel group, repeat dose study to evaluate the safety,tolerability, pharmacokinetics and antiviral effect of differentdoses and regimens of GW873140 in combination with Kaletra(lopinavir and ritonavir) in HIV-1 infected antiretroviral therapynaive subjects
- Conditions
- GW873140 in combination with Kaletra(lopinavir and ritonavir) in HIV-1 infected antiretroviral therapynaive subjectsMedDRA version: 6.1Level: PTClassification code 10020161
- Registration Number
- EUCTR2004-003865-33-IT
- Lead Sponsor
- GLAXO SMITHKLINE
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- 175
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
Name Time Method Main Objective: ;Secondary Objective: ;Primary end point(s):
- Secondary Outcome Measures
Name Time Method