Figures & data
Figure 1. Subject disposition (July 2008). *Reasons for discontinuation from the phase III studies have been reported elsewhereCitation11; †1 subject withdrew consent prior to receiving romiplostim.
![Figure 1. Subject disposition (July 2008). *Reasons for discontinuation from the phase III studies have been reported elsewhereCitation11; †1 subject withdrew consent prior to receiving romiplostim.](/cms/asset/d6c3c07c-e642-402a-9b56-f4925f998f01/yhem_a_11753998_f0001_b.jpg)
Figure 2. (A) Corticosteroid use decreased in romiplostim-treated patients during two, 6-month, phase III studies. Percentages calculated from n = number of subjects remaining on study at the start of the relevant time period. (B) Prednisone dose decreased in patients continuing to receive corticosteroids during the phase III studies. N = Number of subjects receiving prednisone-type corticosteroids during the phase III studies; n = number of subjects receiving prednisone-type corticosteroids at specified time point. (C) Corticosteroid use decreased significantly over time in patients treated with romiplostim for up to 3 years in an open-label extension study. n = number of subjects remaining on study.
![Figure 2. (A) Corticosteroid use decreased in romiplostim-treated patients during two, 6-month, phase III studies. Percentages calculated from n = number of subjects remaining on study at the start of the relevant time period. (B) Prednisone dose decreased in patients continuing to receive corticosteroids during the phase III studies. N = Number of subjects receiving prednisone-type corticosteroids during the phase III studies; n = number of subjects receiving prednisone-type corticosteroids at specified time point. (C) Corticosteroid use decreased significantly over time in patients treated with romiplostim for up to 3 years in an open-label extension study. n = number of subjects remaining on study.](/cms/asset/c2f1dc53-693c-4c4b-9721-a56545f5b71b/yhem_a_11753998_f0002_b.jpg)