A Study of Stem Cells and Filgrastim

Sponsor
National Institute of Allergy and Infectious Diseases (NIAID) (NIH)
Overall Status
Completed
CT.gov ID
NCT00001071
Collaborator
(none)
24
2
12

Study Details

Study Description

Brief Summary

To determine the safety of stem cell harvesting after administration of filgrastim ( G-CSF ) to mobilize bone marrow stem cells into the peripheral blood in patients at various stages of HIV-1 infection as well as in HIV-negative volunteers. To determine the surface phenotypic and functional characteristics as well as the viral load in the stem cells obtained following this procedure.

Condition or Disease Intervention/Treatment Phase
N/A

Detailed Description

Patients and volunteers receive seven daily subcutaneous injections of G-CSF. On days 5 and 6 of drug administration, patients have peripheral blood mononuclear cells harvested by leukapheresis. HIV-positive patients are stratified into three cohorts based on CD4 count and presence of symptoms. If no increase in number of harvested stem cells and no grade 4 bone pain toxicity occur in two of the first three patients in a cohort, then the last three patients in that cohort will receive a dose escalation. Patients are followed for 24 weeks.

Study Design

Study Type:
Interventional
Primary Purpose:
Treatment
Official Title:
A Pilot Study of Stem Cell Mobilization and Harvesting From the Peripheral Blood Using Filgrastim
Actual Study Completion Date :
Oct 1, 1998

Outcome Measures

Primary Outcome Measures

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes

    Inclusion Criteria

    Concurrent Medication:
    Allowed:
    • PCP prophylaxis.

    • Antiretroviral therapy in patients with CD4 counts <= 500 cells/mm3.

    • Narcotic analgesics for grade 3/4 bone pain toxicity.

    Patients must have:
    • HIV infection.

    • HIV infected patients with CD4 count > 500 cells/mm3 must be asymptomatic. Patients with CD4 count 200-500 cells/mm3 may be either asymptomatic or symptomatic but must not have AIDS. Patients with CD4 count < 200 cells/mm3 may or may not have AIDS-defining conditions.

    • No antiretroviral therapy within the past 30 days in patients with asymptomatic disease and CD4 count > 500 cells/mm3.

    • Stable antiretroviral therapy for the past 60 days if CD4 count <= 500 cells/mm3.

    • Suitable venous access.

    Prior Medication:
    Allowed:
    • Prior antiretroviral therapy.

    Exclusion Criteria

    Co-existing Condition:
    Patients with the following symptoms or conditions are excluded:
    • Current malignancy.

    • Any medication condition that interferes with study evaluation.

    • Known hypersensitivity to E. coli-derived proteins (e.g., insulin, human growth hormones).

    Concurrent Medication:
    Excluded:
    • Acute treatment for serious opportunistic infection.

    • Systemic cytotoxic chemotherapy.

    Concurrent Treatment:
    Excluded:
    • Systemic radiation therapy.
    Patients with the following prior conditions are excluded:
    • Prior malignancy.

    • Leukapheresis or lymphopheresis within the past 180 days.

    • Significant active CNS disease or seizures within the past year.

    Prior Medication:
    Excluded:
    • G-CSF or GM-CSF within the past 6 months.

    • Investigational antiretrovirals within the past 30 days.

    • Treatment for opportunistic infection within the past 14 days.

    Active alcohol or substance abuse.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 UCLA CARE Center CRS Los Angeles California United States 90095
    2 University of Colorado Hospital CRS Aurora Colorado United States

    Sponsors and Collaborators

    • National Institute of Allergy and Infectious Diseases (NIAID)

    Investigators

    • Study Chair: Schooley R,
    • Study Chair: Miles S,
    • Study Chair: Pomerantz R,

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    National Institute of Allergy and Infectious Diseases (NIAID)
    ClinicalTrials.gov Identifier:
    NCT00001071
    Other Study ID Numbers:
    • ACTG 285
    • 11261
    First Posted:
    Aug 31, 2001
    Last Update Posted:
    Nov 4, 2021
    Last Verified:
    Oct 1, 2021
    Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID)
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 4, 2021