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A Study of Viracept in HIV-Positive Women

Phase 2
Completed
Conditions
HIV Infections
Registration Number
NCT00002171
Lead Sponsor
Agouron Pharmaceuticals
Brief Summary

The purpose of this study is to see if it is safe and effective to give Viracept plus stavudine (d4T) plus lamivudine (3TC) to HIV-positive women with a CD4 count \<= 400 cells/mm3. This study also examines how the body handles Viracept when given with d4T and 3TC.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (4)

Univ of Alabama at Birmingham

🇺🇸

Birmingham, Alabama, United States

Baylor Univ

🇺🇸

Houston, Texas, United States

HIV Outpatient Clinics / LA State Univ Med Ctr

🇺🇸

New Orleans, Louisiana, United States

Univ of Southern California / LA County USC Med Cntr

🇺🇸

Los Angeles, California, United States

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