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A Study of Indinavir Sulfate Given Together With Stavudine to HIV-Positive Patients

One Year Study in HIV-1 Seropositive, AZT-Experienced Patients to Evaluate the Safety and Efficacy of MK-639 Administered Concomitantly With Stavudine (d4T)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002354
Enrollment
540
Registered
2001-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2005-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

Keywords

Drug Therapy, Combination, Acquired Immunodeficiency Syndrome, AIDS-Related Complex, Stavudine, HIV Protease Inhibitors, Indinavir

Brief summary

The purpose of this study is to see if it is safe and effective to give indinavir sulfate plus stavudine to HIV-infected patients who have already been treated with zidovudine.

Interventions

DRUGIndinavir sulfate
DRUGStavudine

Sponsors

Merck Sharp & Dohme LLC
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

Concurrent Medication: Allowed: * Prophylaxis with aerosolized pentamidine, topical antifungals, TMP / SMX, dapsone, or isoniazid. Patients must have: * HIV infection. * CD4 count 50 - 500 cells/mm3. * Prior AZT use for more than 6 months OR documented intolerance to AZT with more than 6 months use of another anti-HIV therapy other than d4T or any protease inhibitor. * No active opportunistic infection or visceral Kaposi's sarcoma. NOTE: * Patients with hemophilia may be enrolled at discretion of investigator.

Exclusion criteria

Co-existing Condition: Patients with the following symptoms or conditions are excluded: * Symptomatic neuropathy. * Acute hepatitis. Concurrent Medication: Excluded: * Antiretrovirals other than specified in protocol. * Chronic therapy for an active opportunistic infection. * Immunosuppressive therapy. Prior Medication: Excluded: * Any prior protease inhibitor or d4T. * Any nucleoside analogs within 2 weeks prior to study entry. * Investigational agents or immunomodulators within 30 days prior to study entry. Required: * More than 6 months of prior AZT unless intolerant, in which case more than 6 months of another anti-HIV therapy (other than protease inhibitors or d4T).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026