A Phase I/II Pilot Study of Simultaneously Administered Rhu GM-CSF ( CHO Cell ) and Azidothymidine ( AZT ) in Patients With Severe HIV Infection and Leukopenia: Pharmacokinetics and Feasibility
HIV Infections, Cytopenias
About this trial
This is an interventional treatment trial for HIV Infections focused on measuring Neutropenia, Drug Interactions, Granulocyte-Macrophage Colony-Stimulating Factor, Acquired Immunodeficiency Syndrome, Zidovudine
Eligibility Criteria
Inclusion Criteria Concurrent Treatment: Allowed: Minimal local irradiation for tumors. Patients must have: Diagnosis of AIDS or AIDS related complex (ARC). Neutropenia, due either to zidovudine (AZT) or HIV infection. Life expectancy = or > 6 months. Exclusion Criteria Co-existing Condition: Patients with the following conditions or symptoms are excluded: Significant malabsorption as defined by greater than 10 percent weight loss and one or more of the following: Serum carotene less than 75 IU/ml. Vitamin A level less than 75 IU/ml. More than 4 foul-smelling or greasy stools per day. Other criteria of malabsorption. Kaposi's sarcoma (KS) or other tumor which is likely to require specific antitumor therapy during study, other than minimal local irradiation. Active, life-threatening infection with bacterial, viral, fungal, or protozoan pathogens or fever of 39 degrees C within 10 days of study entry, unless it is apparent that the fever is not due to a severe underlying infection. Concurrent Medication: Excluded within 4 weeks of study entry: Any investigational drug. Immunomodulating agents. Hormonal therapy. Cytolytic chemotherapeutic agents. Antiretroviral agent other than zidovudine (AZT). Excluded within 4 months of study entry: Suramin. Excluded within 3 months of study entry: Ribavirin. Patients with the following are excluded: Significant malabsorption. Tumor likely to require specific antitumor therapy during study. Other significant medical problems and conditions specified in Patient Exclusion Co-Existing Conditions. Uncorrected nutritional deficiencies that may contribute to neutropenia. Hypersensitivity to zidovudine (AZT) or other nucleoside analogs. Profound dementia or altered mental status that would prohibit the giving of informed consent. Prior Treatment: Excluded within 1 month of study entry: Transfusion. Excluded within 4 weeks of study entry: Radiation therapy to greater than 100 cm2 body area. Current drug or alcohol abuse. Unprotected sexual behavior or other activities which might introduce a new inoculation of HIV during the study. Patients must be willing to refrain from unprotected sexual or other activities which might introduce a new inoculum of HIV during the study.
Sites / Locations
- Natl Cancer Institute