Expired Study
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Bethesda, Maryland 20892


Purpose:

Background: - The drug filgrastim (rGCSF) increases the number of blood-forming cells in the bloodstream. These cells can be collected from donors bloodstreams and used for transplant. Studies have shown that rGCSF is present in the breast milk of nursing mothers who are taking it. Based on these studies, it is now recommended that a nursing mother should not breastfeed from the time she receives the first dose of the drug until 2 days after the final dose. Researchers want to study the amount of the drug and its effect on the cells present in donor blood and breast milk. They hope to better understand the effects of this drug on breast milk. Objectives: - To understand the effects of filgrastim on breast milk. Eligibility: - Women enrolled in NIH protocol 00-CC-0165 and currently breastfeeding. Design: - Participants will receive rGCSF daily for 5 days. They will have blood taken daily. - Participants will get a freezer bag containing 10 sterile, labeled containers for breast milk collection. - Participants will transfer some of the breast milk they pump into one of the containers. They will write the date and time the milk was collected on the container. They will freeze the samples. Any remaining milk should be disposed of. - Participants will bring the samples to NIH on the day of their stem cell collection procedure. - For days 1 and 2 after stem cell collection, participants will continue to collect and freeze breast milk samples and dispose of any remaining milk. - For days 3 5 after stem cell collection, participants will collect and freeze samples. They can also resume normal breastfeeding. - A research nurse will arrange to collect the samples.


Study summary:

Recombinant human granulocyte colony stimulating factor (rhGCSF) is routinely administered to volunteer peripheral blood stem cell (PBSC) donors in the National Marrow Donor Program (NMDP). Information about the excretion and pharmacokinetics of rhGCSF into human breast milk, however, is extremely limited. Two case reports exist, the first demonstrating only that subcutaneously administered rhGCSF is present in breast milk,1 and the second demonstrating that rhGCSF is not only present, but also remains in breast milk for two days after discontinuation of the medication.2 Based on the data from the latter case report, the NMDP suggests that donors abstain from breastfeeding during the administration of rhGCSF and for 48 hours after the last dose of rhGCSF is given. We intend to collect and test breast milk and peripheral blood from one volunteer NMDP donor during the course of her rhGCSF therapy and for 5 days thereafter, with the intention of better characterizing this rare and unique situation. Collected samples will be used for granulocyte colony stimulating factor (GCSF) quantitation and complete blood counts. Additionally, we will collect a single breast milk sample from three rhGCSF-na(SqrRoot) ve volunteers for use as negative control samples for assay calibration.


Criteria:

- INCLUSION CRITERIA: Women enrolled in NIH protocol 00-CC-0165 and currently breastfeeding.


NCT ID:

NCT02322151


Primary Contact:

Principal Investigator
Kathleen A Conry Cantilena, M.D.
National Institutes of Health Clinical Center (CC)


Backup Contact:

N/A


Location Contact:

Bethesda, Maryland 20892
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: November 18, 2017

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