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

Sponsor

National Institute of Allergy and Infectious Diseases (NIAID) (NIH)

Overall Status

Completed

CT.gov ID

NCT00001085

Collaborator

(none)

Enrollment

Locations

6.3

Patients Per Site

Study Details

Study Description

Brief Summary

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.

Condition or Disease	Intervention/Treatment	Phase
HIV Infections	Drug: Amprenavir Drug: Lamivudine Drug: Zidovudine	Phase 2

Detailed Description

In this randomized, double-blind study, patients' HIV RNA is screened 30 days prior to entry. Patients satisfying enrollment criteria must have been on a stable antiretroviral regimen for 30 days prior to study screening and remain on the same regimen until entry. Patients are stratified based on the screening HIV-1 RNA copy number obtained within 30 days of entry: 5,000 - 50,000 copies/ml versus greater than 50,000 copies/ml. In addition, patients are stratified based on previous antiretroviral use: naive versus experienced. Patients are randomized to one of 2 treatment arms: Arm A - 141W94, plus Zidovudine (ZDV) and Lamivudine (3TC) or Arm B - 141W94, plus ZDV placebo and 3TC placebo.

[AS PER AMENDMENT 8/25/97: Patients assigned to the monotherapy arm are advised to discontinue their study medication immediately and initiate antiretroviral therapy with indinavir, nevirapine, stavudine and 3TC, as outlined in ACTG 347 roll-over protocol, ACTG 373. Patients in the three-drug arm continue on study therapy.] [AS PER AMENDMENT 12/19/97: Patients receive study treatment for 56 weeks and are followed through week 68.]

Study Design

Study Type:

Interventional

Primary Purpose:

Treatment

Official Title:

A Randomized, Double-Blind, Phase II Study of 141W94 (VX-478) Monotherapy vs. 141W94 (VX-478) Plus ZDV Plus 3TC in HIV Infected Individuals

Actual Study Completion Date :

Sep 1, 1998

Outcome Measures

Primary Outcome Measures

Eligibility Criteria

Criteria

Ages Eligible for Study:

13 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria

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.

Exclusion Criteria

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.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Alabama Therapeutics CRS	Birmingham	Alabama	United States	35294
2	USC CRS	Los Angeles	California	United States	900331079
3	University of Colorado Hospital CRS	Aurora	Colorado	United States	80262
4	Univ. of Miami AIDS CRS	Miami	Florida	United States	331361013
5	The Ponce de Leon Ctr. CRS	Atlanta	Georgia	United States	30308
6	Northwestern University CRS	Chicago	Illinois	United States	60611
7	Cook County Hosp. CORE Ctr.	Chicago	Illinois	United States	60612
8	Rush Univ. Med. Ctr. ACTG CRS	Chicago	Illinois	United States	60612
9	Bmc Actg Crs	Boston	Massachusetts	United States	02118
10	Beth Israel Deaconess Med. Ctr., ACTG CRS	Boston	Massachusetts	United States	02215
11	St. Louis ConnectCare, Infectious Diseases Clinic	Saint Louis	Missouri	United States	63112
12	Washington U CRS	Saint Louis	Missouri	United States
13	NY Univ. HIV/AIDS CRS	New York	New York	United States	10016
14	Unc Aids Crs	Chapel Hill	North Carolina	United States	275997215
15	Hosp. of the Univ. of Pennsylvania CRS	Philadelphia	Pennsylvania	United States	19104