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A Study of Viracept in HIV-Positive Women



A Study of Viracept in HIV-Positive Women

For Condition: HIV Infections
Status: Completed
Sponsor(s): Agouron Pharmaceuticals ,
Synopsis: 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.
Details:
Eligibility:
Study Type:
  Interventional, Treatment, Placebo Control, Pharmacokinetics Study
Minimum Age/Maximum Age: 13 Years/
Genders: Female
Protocol Entry Criteria: Inclusion Criteria Patients must have: - HIV infection. - CD4 T cell count <= 400 cells/mm3. Exclusion Criteria Prior Medication: Excluded: - Prior therapy or less than 1 month of therapy with d4T and/or 3TC. - Prior protease inhibitor therapy.
Total Enrollment: 

Location and Contact Information:

Baylor Univ
Houston,  Texas,  77009
United States
 

Univ of Southern California / LA County USC Med Cntr
Los Angeles,  California,  90033
United States
 

HIV Outpatient Clinics / LA State Univ Med Ctr
New Orleans,  Louisiana,  70112
United States
 

Univ of Alabama at Birmingham
Birmingham,  Alabama,  35294
United States
 


Additional Information:
Study ID Numbers:
  259D;  Study 534,AG1343 - 534
Study Start Date: 
Record last reviewed: May 1999
Additional information available at: clinicaltrials.gov
Clinicaltrials.gov Reference link: NCT00002171

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4. Pneumococcal Vaccine and Routine Pediatric Immunizations in HIV-Infected Children Receiving Anti-HIV Drugs

5. Study Of A New Tablet Containing Two FDA-Approved Drugs In HIV-Infected Patients Who Have Not Received Prior Therapy

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