- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00002322
A Study of Different Doses of Atevirdine Mesylate Plus Zidovudine in HIV-Positive Patients
June 23, 2005 updated by: Pharmacia and Upjohn
Randomized, Double-Blind, Placebo-Controlled Comparative Dose-Response Study of Two Doses of Atevirdine Mesylate (U-87201E) in Combination With Fixed Doses of Zidovudine (AZT) in HIV+ Patients
To determine the tolerance and antiviral response of two different doses of atevirdine mesylate (U-87201E) in symptomatic HIV-positive patients with CD4 counts of 50-350 cells/mm3, who also take zidovudine (AZT).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Patients are randomized to 1 of 3 treatment groups: U-87201E at 1 of 2 doses or placebo administered every 8 hours.
Patients must have taken AZT for at least 3 months prior to randomization.
Study Type
Interventional
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
California
-
Los Angeles, California, United States, 90033
- Los Angeles County / Health Research Assoc / Drew Med Ctr
-
Orange, California, United States, 92668
- UCI Med Ctr
-
San Francisco, California, United States, 94114
- Davies Med Ctr
-
-
Florida
-
Tampa, Florida, United States, 33614
- Infectious Disease Research Institute Inc
-
-
Maryland
-
Baltimore, Maryland, United States, 212052196
- Johns Hopkins Hosp
-
-
Massachusetts
-
Boston, Massachusetts, United States, 02118
- Boston City Hosp / FGH-1
-
-
New Jersey
-
East Orange, New Jersey, United States, 07018
- East Orange Veterans Administration Med Ctr
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, United States, 19107
- Buckley Braffman Stern Med Associates
-
-
Rhode Island
-
Pawtucket, Rhode Island, United States, 02860
- Mem Hosp of Rhode Island
-
-
Texas
-
Houston, Texas, United States, 77004
- Park Plaza Hosp
-
San Antonio, Texas, United States, 78284
- Univ TX San Antonio Health Science Ctr
-
-
Wisconsin
-
Milwaukee, Wisconsin, United States, 53202
- Wisconsin Community - Based Research Consortium
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
13 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria
Concurrent Medication:
Allowed:
- Primary or secondary prophylaxis for opportunistic infections.
Patients must have:
- HIV infection.
- Symptoms (currently or prior to enrollment) included in Category B or C of CDC classification, although THE FOLLOWING CURRENT ACUTE MEDICAL CONDITIONS ARE NOT ALLOWED:
- Cryptococcosis
- Pneumocystis carinii pneumonia
- Herpes zoster
- Histoplasmosis
- CMV
- Hepatic or renal disease
- Lymphoma.
- CD4 count 50 - 350 cells/mm3 within 14 days prior to study entry.
- Ongoing therapy with AZT at 500 - 600 mg total daily dose for at least 3 months prior to study entry.
- Consent of parent, guardian, or person with power of attorney if less than 18 years of age.
Exclusion Criteria
Co-existing Condition:
Patients with the following conditions are excluded:
- Intolerance to AZT.
- Current diagnosis of malignancy for which systemic therapy will be required during the study.
Concurrent Medication:
Excluded:
- Any other investigational drugs.
Prior Medication:
Excluded:
- Cytotoxic chemotherapy within 1 month prior to study entry.
- Prior U-87201E or any other non-nucleoside antiretroviral medications, including but not limited to nevirapine, TIBO R-82150 or TIBO R-82913, L-697639 or L-696229, U-90152S, or any protease inhibitors.
- Antiretroviral agents other than AZT within 3 months prior to study entry.
Required:
- AZT for at least 3 months prior to study entry. Present use of excessive alcohol or illicit drugs.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Masking: Double
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Registration Dates
First Submitted
November 2, 1999
First Submitted That Met QC Criteria
August 30, 2001
First Posted (Estimate)
August 31, 2001
Study Record Updates
Last Update Posted (Estimate)
June 24, 2005
Last Update Submitted That Met QC Criteria
June 23, 2005
Last Verified
November 1, 1996
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- RNA Virus Infections
- Virus Diseases
- Infections
- Blood-Borne Infections
- Communicable Diseases
- Sexually Transmitted Diseases, Viral
- Sexually Transmitted Diseases
- Lentivirus Infections
- Retroviridae Infections
- Immunologic Deficiency Syndromes
- Immune System Diseases
- HIV Infections
- Molecular Mechanisms of Pharmacological Action
- Anti-Infective Agents
- Antiviral Agents
- Reverse Transcriptase Inhibitors
- Nucleic Acid Synthesis Inhibitors
- Enzyme Inhibitors
- Anti-HIV Agents
- Anti-Retroviral Agents
- Antimetabolites
- Zidovudine
- Atevirdine
Other Study ID Numbers
- 210A
- M/3330/0018
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on HIV Infections
-
University of MinnesotaWithdrawnHIV Infections | HIV/AIDS | Hiv | AIDS | Aids/Hiv Problem | AIDS and InfectionsUnited States
-
University of California, San DiegoUniversity of California, Los Angeles; University of Southern California; California... and other collaboratorsCompleted
-
Gérond'ifRecruiting
-
University of California, DavisCompleted
-
University of California, San DiegoNational Center for Complementary and Integrative Health (NCCIH)CompletedHIV PositiveUnited States
-
University of ChicagoUniversity of Athens; National Development and Research Institutes, Inc.Completed
-
HIV Prevention Trials NetworkNational Institute on Drug Abuse (NIDA); National Institute of Allergy and...CompletedHIV PositiveIndonesia, Ukraine, Vietnam
-
University of ZimbabweCompleted
-
Florida International UniversityCompleted
-
Boston Children's HospitalNational Institute on Minority Health and Health Disparities (NIMHD)Completed
Clinical Trials on Zidovudine
-
Glaxo WellcomeUnknownHIV InfectionsUnited States
-
Institut de Recherche pour le DeveloppementEunice Kennedy Shriver National Institute of Child Health and Human Development... and other collaboratorsCompletedHIV Infections | PregnancyThailand
-
Glaxo WellcomeCompleted
-
National Institute of Allergy and Infectious Diseases...Eunice Kennedy Shriver National Institute of Child Health and Human Development...Completed
-
Glaxo WellcomeCompleted
-
Glaxo WellcomeCompletedHIV Infections | LipodystrophyUnited States
-
Universidad Peruana Cayetano HerediaMerck Sharp & Dohme LLCCompletedHTLV-I Infections | Tropical Spastic ParaparesisPeru
-
University of Colorado, DenverNational Institute of Allergy and Infectious Diseases (NIAID); University of...Completed
-
ViiV HealthcareCompleted
-
National Institute of Allergy and Infectious Diseases...Eunice Kennedy Shriver National Institute of Child Health and Human Development...CompletedHIV InfectionsUnited States, Puerto Rico