A Study of 141W94 Used Alone or in Combination With Zidovudine Plus 3TC in HIV-Infected Patients

Completed · Phase 2

Conditions studied: HIV Infections

In brief

To determine the proportion of patients whose plasma HIV-1 RNA level remains below a detectable level (less than 500/ml) after 24 weeks of study therapy with either 141W94 monotherapy or 141W94 plus zidovudine (ZDV) and lamivudine (3TC). To determine the safety and tolerability of 141W94 monotherapy and the combination of 141W94 plus 3TC in patients with HIV infection. Although dramatic inhibition of HIV-1 replication is achieved with ritonavir or indinavir monotherapy, in both cases maximum suppression required combination treatment together with nucleoside analog RT inhibitors. This study tests the hypothesis that monotherapy with 141W94 doses that result in Cmin levels far in excess of the IC90 corrected for plasma protein binding for HIV-1 can achieve the same virologic and immunologic effects in terms of magnitude and durability, as has been observed with combinations of other protease inhibitors plus nucleoside analogs.

Key facts

Study ID

NCT00001085

Run by

National Institute of Allergy and Infectious Diseases (NIAID)

People needed

94

Expected to finish

1998-09-01

Last updated by the study team

2021-11-04

Who can join

Age: 13 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Concurrent Medication:
• Allowed:
• Chemoprophylaxis for Pneumocystis carinii pneumonia is required for all patients who have a CD4 cell count <= 200 cells/mm3.
• Topical and/or oral antifungal agents, except for those listed in excluded medications.
• Treatment, maintenance or chemoprophylaxis with approved agents for opportunistic infections as clinically indicated, unless listed in excluded medications.
• All antibiotics as clinically indicated.
• Systemic corticosteroid use for <= 21 days for acute problems is permitted as medically indicated; chronic systemic corticosteroid use is not permitted.
• Recombinant erythropoietin and granulocyte colony-stimulating factor as medically indicated.
• Regularly prescribed medications such as:
• antipyretics, analgesics, allergy medications, antidepressants, sleep medications, oral contraceptives (a barrier method is also required for this study), megestrol acetate, testosterone or any other medications, as medically indicated.
• Alternative therapies such as vitamins, acupuncture and visualization techniques are permitted (excluding herbal medications).
• NOTE:
• Patients should report the use of these therapies; alternative therapies will be recorded.
• Patients must have:
• HIV-1 infection as documented by ELISA and confirmed.
• >= 5,000 HIV-1 RNA copies/ml (within 30 days prior to study entry).
• CD4 cell count >= 50 cells/mm3 within 60 days prior to study entry.
• Signed, informed consent for patients < 18 years of age.
• Prior Medication: Required:
• Patients must be on a stable antiretroviral regimen for 30 days prior to study screening and remain on the same regimen until entry.

You may not qualify if…

• Co-existing Condition:
• Patients with the following symptoms or conditions are excluded:
• Any active infection requiring acute treatment within 14 days prior to entry.
• A malignancy that requires systemic therapy other than minimal Kaposi's sarcoma.
• NOTE:
• Patients with minimal Kaposi's sarcoma, defined as <= 5 cutaneous lesions and no visceral disease or tumor-associated edema, will be allowed to enroll as long as they do not require systemic therapy for Kaposi's sarcoma.
• Patients with the following prior symptoms and conditions are excluded:
• Inability to tolerate ZDV 500-600 mg daily if ZDV was administered previously. Intolerance to ZDV is defined as any grade toxicity that resulted in a dose reduction or termination of ZDV.
• Prior Medication:
• Excluded:
• Any 3TC therapy prior to entry.
• Any HIV-1 protease inhibitor therapy prior to study entry (e.g., saquinavir, ritonavir, indinavir, nelfinavir, 141W94).
• Any immunomodulator therapy within 30 days prior to entry.
• Active immunization within 30 days prior to entry.
• Any antiretroviral therapy change within 30 days prior to study screening.
• Concurrent use of non-protocol specified antiretroviral agents; either investigational or licensed.
• Immunomodulators that affect immunologic or virologic indices such as systemic corticosteroids, thalidomide, or cytokines.
• Concomitant use of rifabutin and/or rifampin.
• Investigational drugs other than 141W94/VX-478.
• Systemic cytotoxic chemotherapy.
• Oral astemizole (Hismanal), carbamazepine (Tegretol), dexamethasone (Decadron), ketoconazole (Nizoral), itraconazole (Sporanox), phenobarbital, phenytoin (Dilantin), terfenadine (Seldane), cisapride (Propulsid), triazolam (Halcion) and midazolam (Versed).
• Herbal medications.

Where it is running

• Alabama Therapeutics CRS — Birmingham, Alabama, United States
• USC CRS — Los Angeles, California, United States
• University of Colorado Hospital CRS — Aurora, Colorado, United States
• Univ. of Miami AIDS CRS — Miami, Florida, United States
• The Ponce de Leon Ctr. CRS — Atlanta, Georgia, United States
• Northwestern University CRS — Chicago, Illinois, United States
• Cook County Hosp. CORE Ctr. — Chicago, Illinois, United States
• Rush Univ. Med. Ctr. ACTG CRS — Chicago, Illinois, United States
• Bmc Actg Crs — Boston, Massachusetts, United States
• Beth Israel Deaconess Med. Ctr., ACTG CRS — Boston, Massachusetts, United States
• St. Louis ConnectCare, Infectious Diseases Clinic — St Louis, Missouri, United States
• Washington U CRS — St Louis, Missouri, United States
• NY Univ. HIV/AIDS CRS — New York, New York, United States
• Unc Aids Crs — Chapel Hill, North Carolina, United States
• Hosp. of the Univ. of Pennsylvania CRS — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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