Safety and Tolerability of Z-100 in Patients With Early HIV Infection
This study has been terminated.
Sponsor:
Zeria Pharmaceutical
Information provided by:
Zeria Pharmaceutical
ClinicalTrials.gov Identifier:
NCT00016692
First received: May 24, 2001
Last updated: April 26, 2006
Last verified: April 2001
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
HIV Infections |
Drug: Z-100 |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Masking: Double-Blind Primary Purpose: Treatment |
| 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 |
Resource links provided by NLM:
Genetics Home Reference related topics:
complement factor I deficiency
MedlinePlus related topics:
HIV/AIDS
U.S. FDA Resources
Further study details as provided by Zeria Pharmaceutical:
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
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.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00016692
Locations
| United States, California | |
| UCSF - San Francisco Gen Hosp | |
| San Francisco, California, United States, 94110 | |
| United States, Illinois | |
| Northwestern Univ Med School | |
| Chicago, Illinois, United States, 60611 | |
| United States, Texas | |
| Univ TX Med Branch | |
| Galveston, Texas, United States, 77555 | |
Sponsors and Collaborators
Zeria Pharmaceutical
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00016692 History of Changes |
| Other Study ID Numbers: | B014, Zeria Protocol 85D10104 |
| Study First Received: | May 24, 2001 |
| Last Updated: | April 26, 2006 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Zeria Pharmaceutical:
|
Drug tolerance Acute Infection |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes |
Immune System Diseases Slow Virus Diseases Specific substance maruyama Adjuvants, Immunologic Immunologic Factors Physiological Effects of Drugs Pharmacologic Actions Antineoplastic Agents Therapeutic Uses |
ClinicalTrials.gov processed this record on May 22, 2013