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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

Primary Purpose

HIV Infections, Cytopenias

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Zidovudine
Sargramostim
Sponsored by
Sandoz
About
Eligibility
Locations
Outcomes
Full info

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

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

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

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
June 23, 2005
Sponsor
Sandoz
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1. Study Identification

Unique Protocol Identification Number
NCT00002006
Brief Title
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
Official Title
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
Study Type
Interventional

2. Study Status

Record Verification Date
January 1990
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Sandoz

4. Oversight

5. Study Description

Brief Summary
To assess the safety and efficacy of subcutaneously administered sargramostim ( granulocyte-macrophage colony-stimulating factor; GM-CSF ) in increasing and maintaining the neutrophil count in HIV-infected adults who have developed neutropenia as a result of receiving the antiretroviral agent, zidovudine ( AZT ). To assess the safety and efficacy of subcutaneously administered GM-CSF in increasing and maintaining the neutrophil count in HIV-infected adults with pre-existing neutropenia who are at high risk of developing hematologic intolerance while receiving the antiretroviral agent, AZT, for the first time. To assess the potential therapeutic benefit of concomitant GM-CSF and AZT on the natural history of HIV infection and associated infectious complications.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Cytopenias
Keywords
Neutropenia, Drug Interactions, Granulocyte-Macrophage Colony-Stimulating Factor, Acquired Immunodeficiency Syndrome, Zidovudine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Zidovudine
Intervention Type
Drug
Intervention Name(s)
Sargramostim

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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.
Facility Information:
Facility Name
Natl Cancer Institute
City
Bethesda
State/Province
Maryland
ZIP/Postal Code
20892
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
1742482
Citation
Levine JD, Allan JD, Tessitore JH, Falcone N, Galasso F, Israel RJ, Groopman JE. Recombinant human granulocyte-macrophage colony-stimulating factor ameliorates zidovudine-induced neutropenia in patients with acquired immunodeficiency syndrome (AIDS)/AIDS-related complex. Blood. 1991 Dec 15;78(12):3148-54.
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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

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