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| Name | Class |
|---|---|
| Amgen | INDUSTRY |
Hypothesis: pegfilgrastim at 300 µg/kg in hematological steady state provides an efficient stem cell mobilization in children with malignancies
Design: phase 2 study.
Judgment criterion: percentage of children achieving at least 5x10e6 CD34 cells with a standard apheresis (less than 2 blood volume processed)
Patients: consecutively referred for HSC mobilization. At least 17 days after the previous chemotherapy. No hematological growth factor during the 8 previous days.
Mobilization: one sc injection of 300 µg/kg pegfilgrastim (Neulasta, Amgen)
Evaluation during the study: CD34 circulating cells from day 2 to day 7 ; AE recording
Judgment criterion: percentage of children achieving at least 5x10e6 CD34 cells with a standard apheresis (less than 2 blood volume processed)
Analysis: sequential Bayesian study
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Pegfilgrastim (drug) | Drug |
| Measure | Description | Time Frame |
|---|---|---|
| percentage of children achieving at least 5x10e6 CD34 cells with a standard apheresis (less than 2 blood volume processed) |
| Measure | Description | Time Frame |
|---|---|---|
| Side effects Number of apheresis required to achieved a graft of at least 5x10e6 CD34 cells |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Etienne Merlin, MD | University Hospital, Clermont-Ferrand | Principal Investigator |
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| ID | Term |
|---|---|
| D009369 | Neoplasms |
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| ID | Term |
|---|---|
| C455861 | pegfilgrastim |
| D004364 | Pharmaceutical Preparations |
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