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Comparison of Two Dosing Regimens of GW433908/Ritonavir Versus Lopinavir/Ritonavir for 48 Weeks in HIV Patients Who Have Taken Protease Inhibitors and Experienced Virological Failure

Phase 3
Conditions
HIV Infections
Registration Number
NCT00025727
Lead Sponsor
GlaxoSmithKline
Brief Summary

The purpose of this study is to test 2 different dosing regimens of GW433908/ritonavir (RTV) versus lopinavir (LPV)/RTV when each is given with 2 active reverse transcriptase inhibitors (RTIs), in patients who have taken anti-HIV drugs without success.

Detailed Description

Patients will receive 2 dosing regimens of GW433908/RTV or LPV/RTV, in combination with 2 active RTIs, after failing their first or second protease inhibitor-containing regimen. Patients are required to be on therapy at time of screening and must remain on this therapy until Day 1.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
330
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (32)

Phoenix Body Positive

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Phoenix, Arizona, United States

Ocean View Internal Medicine

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Long Beach, California, United States

Bisher Akil

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Los Angeles, California, United States

Tower ID Med Associates

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Los Angeles, California, United States

Orange Coast Med Group

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Newport Beach, California, United States

Pacific Horizons Med Group

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San Francisco, California, United States

Denver Inf Disease Consultants

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Denver, Colorado, United States

Physicans Home Service

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Washington, District of Columbia, United States

IDC Research Initiative

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Altamonte Springs, Florida, United States

Bach and Godofsky

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Bradenton, Florida, United States

Scroll for more (22 remaining)
Phoenix Body Positive
๐Ÿ‡บ๐Ÿ‡ธPhoenix, Arizona, United States

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