Status:
COMPLETED
Induction-Maintenance With Atazanavir in HIV Naïve Patients (The INDUMA Study)
Lead Sponsor:
Bristol-Myers Squibb
Conditions:
HIV Infections
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
The purpose of this study is to compare the proportion of subjects with HIV-1 RNA viral load \< 50 c/mL through Week 48 of the Maintenance Phase among HIV-infected subjects with an initial undetectabl...
Eligibility Criteria
Inclusion
- Treatment naive HIV-1 infected subjects ( \< 10 days of treatment with any ARV).
- Subjects who have an HIV-1 RNA level ≥ 5000 c/mL at screening.
- Subjects who have a CD4 count ≥ 50 cells/mm3.
- Men and women, ages 18 years of age or older (or minimum age as determined by local regulatory or as legal requirements dictate).
- Both females of child-bearing potential and males must utilize effective barrier contraception. Other contraception in addition to barrier methods is permitted; refer to the Investigator Brochure for details regarding potential interactions with ATV and some oral contraceptives
Exclusion
- WOCBP who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and for up to 8 weeks after the study.
- WOCBP using a prohibited contraceptive method. Caution is warranted with coadministration of oral contraceptives (ethinyl estradiol and norethindrone) - see Investigator Brochure for details
- Women who are pregnant or breastfeeding
- Women with a positive pregnancy test on enrollment or prior to study drug administration.
- Presence of a newly diagnosed HIV-related opportunistic infection or any medical condition requiring acute therapy at the time of enrollment
- Primary HIV infection
- Medical History and Concurrent Diseases
- Active alcohol or substance use sufficient, in the investigator's opinion, to prevent adequate compliance with study therapy or to increase the risk of developing pancreatitis or chemical hepatitis Physical and Laboratory Test Findings
- Screening laboratory values measured as follows:
- Grade IV glucose,
- Grade IV electrolytes,
- Grade IV transaminases,
- Grade IV hematology.
- Hypersensitivity to any component of the formulation of study drug
- Prior history of taking any ARV for more than 10 days
- Concomitant administration of tenofovir (TDF).
- Refer to Section 6.4.1 which details all prohibited therapies
Key Trial Info
Start Date :
November 1 2005
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2008
Estimated Enrollment :
252 Patients enrolled
Trial Details
Trial ID
NCT00207142
Start Date
November 1 2005
End Date
January 1 2008
Last Update
January 12 2010
Active Locations (27)
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1
Local Institution
Tallinn, Estonia
2
Local Institution
Le Kremlin-Bicêtre, France
3
Local Institution
Orléans, France
4
Local Institution
Paris, France