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OpenTrials
Completed

NCT Number: NCT00084253

Study of Boosted Atazanavir (ATV) Versus Non-boosted ATV in Naive Patients

The purpose of this study is to find out if 300 mg of ATV plus 100 mg of ritonavir (RTV) works as well as 400 mg of ATV alone as part of a regimen with stavudine XR and lamivudine to slow or stop the progression of HIV infection in patients who have never used anti-HIV drugs.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Various locations within the US

Call For Information, New Jersey, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed Informed Consent
  • HIV RNA greater than or equal 200 copies/mL at screening
  • 18 years old or older
  • Must use barrier contraception
  • Women of child-bearing potential must have a negative serum or urine pregnancy test within 72 hours before beginning to take the study medications

Exclusion criteria

  • Unable or unwilling to use acceptable method of birth control for the entire study period including 8 weeks after the study
  • Women using oral contraceptives, pregnant or breastfeeding women
  • Women who have a positive pregnancy test on enrollment or before beginning to take the study medications
  • People who have a life expectancy of greater than 12 months
  • Newly diagnosed HIV-related OI or any medical condition requiring acute therapy at the time of enrollment
  • Any antiretroviral therapy within 30 days prior to screening
  • Any prior antiretroviral therapy (greater than 30 days of NRTI and/or greater than 7 days of non-nucleoside reverse-transcriptase inhibitor (NNRTI) or protease inhibitor therapies)
  • Any of the following conditions: Cushings Syndrome, Gilbert's Syndrome, untreated hypothyroidism or hyperthyroidism, suspected primary (acute) HIV infection, obstructive liver disease, proven or suspected acute hepatitis in the 30 days prior to study entry, Intractable diarrhea (at greater than 6 loose stools per day for at least 78 consecutive days) within 30 days prior to study entry, history of hemophilia, history of acute or chronic pancreatitis, presence of cardiomyopathy (due to any cause) or any significant cardiovascular disease, such as unstable ischemic heart disease
  • Active alcohol or substance abuse
  • History or signs and symptoms of bilateral peripheral neuropathy greater than grade 2 at the time of screening
  • Previous therapy with myelosuppressive, neurotoxic, pancreatotoxic, hepatotoxic, or cytotoxic potential within 3 months of study start or the expected need for such therapy or therapy with methadone or ribavirin/interferons or treatment with neurotoxic drugs or drugs that affect CYP3A4
  • Inability to swallow capsules

Treatment and study plan

Atazanavir/ Stavidine / Lamivudine

Drug

Capsules, Oral, ATV (2 x 200 mg) QD + 3TC (2 x 150 mg) QD + Zerit XR (1 x 100 mg) QD, Once daily, 96 weeks.

Other names: Reyataz

Atazanavir-Ritonavir/ Stavidine / Lamivudine

Drug

Capsules, Oral, ATV (2 x 150 mg) QD + RTV (1 x 100 mg) QD + 3TC (2 x 150 mg) QD + Zerit XR (1 x 100 mg) QD*, Once daily, 96 weeks.

Other names: Reyataz

Primary outcomes

  1. To compare the proportion of subjects responding to treatment with HIV RNA levels < LOQ (400 c/mL) through Week 48 in treatment naive subjects for ATV and ATV/RTV (each combined with 3TC and d4T XR).

Sponsors and collaborators

Lead sponsor

Bristol-Myers Squibb

Industry

Registry information

Official study title

Phase IV Study of Boosted Atazanavir (ATV) Versus Non-boosted ATV in Naive Patients

Important dates

Study start
2004
Primary completion
2006
First posted
Jun 11, 2004
Registry last updated
Mar 5, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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