search
Back to results

A Comparison of 141W94 and Indinavir in HIV-Infected Patients

Primary Purpose

HIV Infections

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Indinavir sulfate
Amprenavir
Sponsored by
Glaxo Wellcome
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring HIV-1, Drug Therapy, Combination, HIV Protease Inhibitors, Indinavir, RNA, Viral, VX 478, Reverse Transcriptase Inhibitors, Anti-HIV Agents, Viral Load

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria Patients must have: Documented HIV infection. HIV RNA >= 400 copies/ml within 14 days prior to randomized study drug administration. No active AIDS-defining opportunistic infection or disease. Signed, informed consent from parent or legal guardian of patients less than 18 years of age. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Unlikely to complete the randomized dosing period. Malabsorption syndrome or other gastrointestinal dysfunction that might interfere with drug absorption or ability to take oral medications. Serious medical conditions (e.g., diabetes, cardiac dysfunction, hepatitis) that would compromise patient safety. Concurrent Medication: Excluded: Cytotoxic chemotherapeutic agents (except local treatment for Kaposi's sarcoma). Investigational treatments (treatment through Treatment IND or expanded-access programs are evaluated individually). Immunomodulating agents such as systemic, high-dose corticosteroids, interleukins, or interferons. Terfenadine, astemizole, cisapride, triazolam, midazolam, and ergotamine/dihydroergotamine-containing regimens. Concurrent Treatment: Excluded: Radiation therapy (except local treatment for Kaposi's sarcoma). Patients with the following prior conditions are excluded: Clinically relevant pancreatitis or hepatitis within the last 6 months. Prior Medication: Excluded: Cytotoxic chemotherapeutic agents within 30 days of study drug administration (except local treatment for Kaposi's sarcoma). Protease inhibitor therapy. Dose of vaccine through an investigational HIV vaccine trial within the 3 months prior to study drug administration. Immunomodulating agents such as systemic, high-dose corticosteroids, interleukins, or interferons within 30 days of study drug administration. Prior Treatment: Excluded: Radiation therapy within 30 days prior to study drug administration (except local treatment for Kaposi's sarcoma). Risk Behavior: Excluded: Current alcohol or illicit drug use that may interfere with drug absorption or ability to take oral medication. Required: NRTI therapy at day of entry and up to screening. Required: >= 12 weeks of NRTI therapy.

Sites / Locations

  • East Bay AIDS Ctr
  • AIDS Healthcare Foundation
  • Saint Francis Mem Hosp
  • ViRx Inc
  • Univ of Colorado Health Sciences Ctr
  • Whitman Walker Clinic Inc
  • CRI of South Florida
  • Community Research Initiative of Central Florida
  • Univ of Miami Dept of Medicine
  • Northwestern Univ Med School
  • Tulane Univ Med School
  • Boston Med Ctr / Evans - 556
  • Beth Israel Deaconess Med Ctr
  • Univ of Nebraska Med Ctr
  • Community Research Initiative on AIDS
  • Harlem Hosp
  • The Nalle Clinic / Clinical Research Dept
  • Med College of Ohio / Division of Infectious Diseases
  • The Research and Education Group
  • Methodist Hosp
  • Community Oriented Primary Care
  • Univ of Texas Med Branch
  • Baylor College of Medicine / Dept of Medicine
  • Hampton Roads Med Specialists

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
June 23, 2005
Sponsor
Glaxo Wellcome
search

1. Study Identification

Unique Protocol Identification Number
NCT00002202
Brief Title
A Comparison of 141W94 and Indinavir in HIV-Infected Patients
Official Title
A Phase III Trial to Compare the Safety and Antiviral Efficacy of 141W94 With Indinavir in Combination With Nucleoside Reverse Transcriptase Inhibitor (NRTI) Therapy, in NRTI-Experienced, Protease Inhibitor (PI)-Naive, HIV-1-Infected Patients.
Study Type
Interventional

2. Study Status

Record Verification Date
November 1998
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Glaxo Wellcome

4. Oversight

5. Study Description

Brief Summary
The purpose of this study is to see if 141W94 is as safe and effective as indinavir when used with nucleoside reverse transcriptase inhibitors (NRTIs) for 48 weeks. This study also examines what effect other drugs have on how the body handles 141W94.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
HIV-1, Drug Therapy, Combination, HIV Protease Inhibitors, Indinavir, RNA, Viral, VX 478, Reverse Transcriptase Inhibitors, Anti-HIV Agents, Viral Load

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Enrollment
460 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Indinavir sulfate
Intervention Type
Drug
Intervention Name(s)
Amprenavir

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patients must have: Documented HIV infection. HIV RNA >= 400 copies/ml within 14 days prior to randomized study drug administration. No active AIDS-defining opportunistic infection or disease. Signed, informed consent from parent or legal guardian of patients less than 18 years of age. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Unlikely to complete the randomized dosing period. Malabsorption syndrome or other gastrointestinal dysfunction that might interfere with drug absorption or ability to take oral medications. Serious medical conditions (e.g., diabetes, cardiac dysfunction, hepatitis) that would compromise patient safety. Concurrent Medication: Excluded: Cytotoxic chemotherapeutic agents (except local treatment for Kaposi's sarcoma). Investigational treatments (treatment through Treatment IND or expanded-access programs are evaluated individually). Immunomodulating agents such as systemic, high-dose corticosteroids, interleukins, or interferons. Terfenadine, astemizole, cisapride, triazolam, midazolam, and ergotamine/dihydroergotamine-containing regimens. Concurrent Treatment: Excluded: Radiation therapy (except local treatment for Kaposi's sarcoma). Patients with the following prior conditions are excluded: Clinically relevant pancreatitis or hepatitis within the last 6 months. Prior Medication: Excluded: Cytotoxic chemotherapeutic agents within 30 days of study drug administration (except local treatment for Kaposi's sarcoma). Protease inhibitor therapy. Dose of vaccine through an investigational HIV vaccine trial within the 3 months prior to study drug administration. Immunomodulating agents such as systemic, high-dose corticosteroids, interleukins, or interferons within 30 days of study drug administration. Prior Treatment: Excluded: Radiation therapy within 30 days prior to study drug administration (except local treatment for Kaposi's sarcoma). Risk Behavior: Excluded: Current alcohol or illicit drug use that may interfere with drug absorption or ability to take oral medication. Required: NRTI therapy at day of entry and up to screening. Required: >= 12 weeks of NRTI therapy.
Facility Information:
Facility Name
East Bay AIDS Ctr
City
Berkeley
State/Province
California
ZIP/Postal Code
94705
Country
United States
Facility Name
AIDS Healthcare Foundation
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
Saint Francis Mem Hosp
City
San Francisco
State/Province
California
ZIP/Postal Code
94109
Country
United States
Facility Name
ViRx Inc
City
San Francisco
State/Province
California
ZIP/Postal Code
94109
Country
United States
Facility Name
Univ of Colorado Health Sciences Ctr
City
Denver
State/Province
Colorado
ZIP/Postal Code
80262
Country
United States
Facility Name
Whitman Walker Clinic Inc
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20009
Country
United States
Facility Name
CRI of South Florida
City
Coral Gables
State/Province
Florida
ZIP/Postal Code
33146
Country
United States
Facility Name
Community Research Initiative of Central Florida
City
Maitland
State/Province
Florida
ZIP/Postal Code
32751
Country
United States
Facility Name
Univ of Miami Dept of Medicine
City
Miami
State/Province
Florida
ZIP/Postal Code
33136
Country
United States
Facility Name
Northwestern Univ Med School
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
Tulane Univ Med School
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
70112
Country
United States
Facility Name
Boston Med Ctr / Evans - 556
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
021182393
Country
United States
Facility Name
Beth Israel Deaconess Med Ctr
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Facility Name
Univ of Nebraska Med Ctr
City
Omaha
State/Province
Nebraska
ZIP/Postal Code
681985400
Country
United States
Facility Name
Community Research Initiative on AIDS
City
New York
State/Province
New York
ZIP/Postal Code
10001
Country
United States
Facility Name
Harlem Hosp
City
New York
State/Province
New York
ZIP/Postal Code
10027
Country
United States
Facility Name
The Nalle Clinic / Clinical Research Dept
City
Charlotte
State/Province
North Carolina
ZIP/Postal Code
28207
Country
United States
Facility Name
Med College of Ohio / Division of Infectious Diseases
City
Toledo
State/Province
Ohio
ZIP/Postal Code
43614
Country
United States
Facility Name
The Research and Education Group
City
Portland
State/Province
Oregon
ZIP/Postal Code
97210
Country
United States
Facility Name
Methodist Hosp
City
Memphis
State/Province
Tennessee
ZIP/Postal Code
38104
Country
United States
Facility Name
Community Oriented Primary Care
City
Dallas
State/Province
Texas
ZIP/Postal Code
75217
Country
United States
Facility Name
Univ of Texas Med Branch
City
Galveston
State/Province
Texas
ZIP/Postal Code
775550835
Country
United States
Facility Name
Baylor College of Medicine / Dept of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
770303498
Country
United States
Facility Name
Hampton Roads Med Specialists
City
Hampton
State/Province
Virginia
ZIP/Postal Code
23666
Country
United States

12. IPD Sharing Statement

Learn more about this trial

A Comparison of 141W94 and Indinavir in HIV-Infected Patients

We'll reach out to this number within 24 hrs