An interventional study of Zidovudine and Sargramostim in HIV Infections and Cytopenias, sponsored by Sandoz. Completed at 1 site in United States. Open to participants aged 6 Months to 12 Years. Per ClinicalTrials.gov, last updated 2005-06-24.
Sponsored by Sandoz · Not applicable, Interventional, and Treatment
To assess the safety and efficacy of subcutaneous sargramostim ( granulocyte-macrophage colony-stimulating factor; GM-CSF ) in increasing and maintaining the granulocyte count in HIV-infected children who have developed granulocytopenia as a result of continuous intravenous ( CIV ) zidovudine ( AZT ). To assess the short-term and long-term effects of concomitant GM-CSF on other hematologic parameters. To assess the potential therapeutic benefit of concomitant GM-CSF and AZT on the natural history of HIV infection and associated infectious complications.
396 studies on the registry are indexed under Neutropenia; 57 are open to participants now.
Browse Neutropenia studies →Sandoz is the lead sponsor of 136 studies on the registry; none are open to participants now.
Of its 10 completed or terminated interventional studies of FDA-regulated products, 5 (50%) have results posted.
Counted across the registry records on this site, refreshed daily.
Concurrent Medication:
Allowed:
Patients must have:
Prior Medication:
Allowed within 48 hours of study entry:
Exclusion Criteria
Co-existing Condition:
Patients with the following conditions or symptoms are excluded:
Patients with the following are excluded:
Prior Medication:
Excluded within 48 hours of study entry:
Prior Treatment:
Excluded within 6 months of study entry:
This study is completed, as verified in Jan 1990. You cannot join it, but the record below documents what was studied.
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