A Study on the Safety and Effectiveness of Twice-Daily Nelfinavir Plus Twice-Daily Indinavir Plus Efavirenz in HIV-Positive Patients Who Have Never Taken Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs) or Protease Inhibitors

Merck Sharp & Dohme (MSD) logo

Merck Sharp & Dohme (MSD)

Status and phase

Completed
Phase 2

Conditions

HIV Infections

Treatments

Drug: Efavirenz
Drug: Nelfinavir mesylate
Drug: Indinavir sulfate

Study type

Interventional

Funder types

Industry

Identifiers

NCT00002235
259G
ICC 602

Details and patient eligibility

About

Indinavir is usually taken three times a day. The purpose of this study is to see if it is safe and effective to take indinavir only twice a day plus nelfinavir (also taken twice a day) and efavirenz (taken once a day).

Full description

Patients receive a treatment regimen consisting of nelfinavir, indinavir, and efavirenz for 48 weeks. During the study, patients are evaluated for changes from baseline in plasma HIV-1 RNA levels and lymphocyte subsets and for development of adverse events and toxicities. After Week 48, patients with documented virologic response are eligible to continue receiving study treatments and to attend scheduled follow-up visits. Patients who experience virologic failure are discontinued from the study.

Sex

All

Ages

13+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

You may be eligible for this study if you:

  • Are HIV-positive.
  • Are at least 13 years old (consent of parent or guardian required if under 18).
  • Have a viral load of at least 10,000 copies/ml within 30 days of study entry.
  • Agree to use a barrier method of birth control, such as condoms, during the study.

Exclusion Criteria

You will not be eligible for this study if you:

  • Have hepatitis.
  • Have any other serious medical condition besides HIV infection.
  • Are allergic to indinavir, nelfinavir, or efavirenz.
  • Have ever taken NNRTIs or protease inhibitors.
  • Have had chemotherapy or radiation therapy within 30 days of study entry. (Local radiation therapy is allowed.)
  • Have taken certain other medications that might affect your immune system such as interleukin-2, interferon, or a vaccine within 30 days of study entry.
  • Are enrolled or plan to enroll in another anti-HIV drug study during this study.
  • Are pregnant or breast-feeding.
  • Abuse alcohol or drugs.

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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