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

This study has been terminated.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00016692
First Posted: August 31, 2001
Last Update Posted: April 27, 2006
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Zeria Pharmaceutical
May 24, 2001
August 31, 2001
April 27, 2006
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Complete list of historical versions of study NCT00016692 on ClinicalTrials.gov Archive Site
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Safety and Tolerability of Z-100 in Patients With Early HIV Infection
A Phase 1b Multicenter Double-Blind, Placebo-Controlled, Randomized Study on the Safety and Tolerability of Z-100 in Early HIV-1 Infected Patients
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.
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Interventional
Phase 1
Masking: Double
Primary Purpose: Treatment
HIV Infections
Drug: Z-100
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
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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.
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00016692
B014
Zeria Protocol 85D10104
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Zeria Pharmaceutical
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Zeria Pharmaceutical
April 2001

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP