Table 1

Effect of romiplostim on bone marrow in rats

Week 5 (date of death)
Week 9 (date of death)
0 μg/kg romiplostim (n = 20)10 μg/kg romiplostim (n = 18)30 μg/kg romiplostim (n = 20)100 μg/kg romiplostim (n = 17)0 μg/kg romiplostim (n = 10)100 μg/kg romiplostim (n = 10)
Femur, n (%)       
    Fibrosis 1 (6) 4 (20) 9 (53) 
    Megakaryocyte hyperplasia 9 (50) 8 (40) 11 (65) 
    Hyperostosis 4 (20) 12 (71) 
Sternum, n (%)       
    Fibrosis 1 (5) 9 (53) 
    Megakaryocyte hyperplasia 8 (44) 8 (40) 10 (59) 
    Hyperostosis 3 (18) 
Mean platelet count, ×109/L 1077 2467 1917 1981 1165 1017 
Week 5 (date of death)
Week 9 (date of death)
0 μg/kg romiplostim (n = 20)10 μg/kg romiplostim (n = 18)30 μg/kg romiplostim (n = 20)100 μg/kg romiplostim (n = 17)0 μg/kg romiplostim (n = 10)100 μg/kg romiplostim (n = 10)
Femur, n (%)       
    Fibrosis 1 (6) 4 (20) 9 (53) 
    Megakaryocyte hyperplasia 9 (50) 8 (40) 11 (65) 
    Hyperostosis 4 (20) 12 (71) 
Sternum, n (%)       
    Fibrosis 1 (5) 9 (53) 
    Megakaryocyte hyperplasia 8 (44) 8 (40) 10 (59) 
    Hyperostosis 3 (18) 
Mean platelet count, ×109/L 1077 2467 1917 1981 1165 1017 

Romiplostim or placebo was administered subcutaneously 3 times per week for 4 weeks. Bone marrow samples were taken from animals killed either 3 days after the last dose of romiplostim (week 5) or after a 4-week recovery period (week 9).

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