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Safety and Tolerability of Z-100 in Patients With Early HIV Infection

Primary Purpose

HIV Infections

Status
Terminated
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Z-100
Sponsored by
Zeria Pharmaceutical
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Drug tolerance, Acute Infection

Eligibility Criteria

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

Inclusion Criteria Patients may be eligible for this study if they: Are HIV positive but do not show symptoms. Are male or female, 18 years or older. Have not received treatment for HIV. Have received treatment but have discontinued HAART for at least 8 weeks prior to screening, have had stable viral loads on at least 2 separate time points at least 1 month apart including screening, and have had stable CD4 levels on at least 2 separate time points at least 1 month apart including screening. Use birth control while on the study and during the follow-up period. Have viral loads of 2,000 to 55,000 copies/ml within 2 weeks of randomization. Have CD4 counts of greater than 350 cells/mm within 2 weeks of randomization. Have a negative serum pregnancy test within 2 weeks of randomization (women able to have children). Exclusion Criteria Patients will not be eligible for this study if they: Have failed HAART treatment. Have opportunistic infection or cancer. Have a history of tuberculosis. Have very abnormal laboratory test results. Have heart, liver, kidney or nervous system conditions. Have serious problems digesting and absorbing food or have serious long-term diarrhea within 4 weeks of randomization. Have received radiation (localized is allowed) or chemotherapy within 30 days before randomization. Have seizure disorders that cannot be controlled. Have received any other drugs that affect the immune system or experimental drugs within 60 days before randomization. Have had any vaccination within 15 days before randomization. Have a mental condition which makes the patient unable to understand what the study is about and what it involves. Have a history of alcohol or drug abuse, unless the investigator feels that it will not interfere with participation in the protocol. Are pregnant or breast-feeding. Have a history of being very sensitive to the study drug or similar drugs.

Sites / Locations

  • UCSF - San Francisco Gen Hosp
  • Northwestern Univ Med School
  • Univ TX Med Branch

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
May 24, 2001
Last Updated
April 26, 2006
Sponsor
Zeria Pharmaceutical
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1. Study Identification

Unique Protocol Identification Number
NCT00016692
Brief Title
Safety and Tolerability of Z-100 in Patients With Early HIV Infection
Official Title
A Phase 1b Multicenter Double-Blind, Placebo-Controlled, Randomized Study on the Safety and Tolerability of Z-100 in Early HIV-1 Infected Patients
Study Type
Interventional

2. Study Status

Record Verification Date
April 2001
Overall Recruitment Status
Terminated
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Zeria Pharmaceutical

4. Oversight

5. Study Description

Brief Summary
The purpose of the study is to see if Z-100 (an investigational drug) treatment is safe in HIV patients who have never received treatment for their HIV, who have not been taking highly active antiretroviral therapy (HAART) for at least 8 weeks, or who have been stable on their current first or second HAART regimen for at least 12 weeks.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections
Keywords
Drug tolerance, Acute Infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Masking
Double

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Z-100

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patients may be eligible for this study if they: Are HIV positive but do not show symptoms. Are male or female, 18 years or older. Have not received treatment for HIV. Have received treatment but have discontinued HAART for at least 8 weeks prior to screening, have had stable viral loads on at least 2 separate time points at least 1 month apart including screening, and have had stable CD4 levels on at least 2 separate time points at least 1 month apart including screening. Use birth control while on the study and during the follow-up period. Have viral loads of 2,000 to 55,000 copies/ml within 2 weeks of randomization. Have CD4 counts of greater than 350 cells/mm within 2 weeks of randomization. Have a negative serum pregnancy test within 2 weeks of randomization (women able to have children). Exclusion Criteria Patients will not be eligible for this study if they: Have failed HAART treatment. Have opportunistic infection or cancer. Have a history of tuberculosis. Have very abnormal laboratory test results. Have heart, liver, kidney or nervous system conditions. Have serious problems digesting and absorbing food or have serious long-term diarrhea within 4 weeks of randomization. Have received radiation (localized is allowed) or chemotherapy within 30 days before randomization. Have seizure disorders that cannot be controlled. Have received any other drugs that affect the immune system or experimental drugs within 60 days before randomization. Have had any vaccination within 15 days before randomization. Have a mental condition which makes the patient unable to understand what the study is about and what it involves. Have a history of alcohol or drug abuse, unless the investigator feels that it will not interfere with participation in the protocol. Are pregnant or breast-feeding. Have a history of being very sensitive to the study drug or similar drugs.
Facility Information:
Facility Name
UCSF - San Francisco Gen Hosp
City
San Francisco
State/Province
California
ZIP/Postal Code
94110
Country
United States
Facility Name
Northwestern Univ Med School
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States
Facility Name
Univ TX Med Branch
City
Galveston
State/Province
Texas
ZIP/Postal Code
77555
Country
United States

12. IPD Sharing Statement

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Safety and Tolerability of Z-100 in Patients With Early HIV Infection

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