16
Participants
Start Date
December 2, 2002
Primary Completion Date
July 19, 2004
Study Completion Date
July 19, 2004
Romiplostim
Administered subcutaneously on day 1 and on day 15 or 22 if the platelet count was ≤ 50 x 10⁹/L and not rising, peak platelet count was ≤ 450 x 10⁹/L and no serious adverse events related to treatment were observed.
Lead Sponsor
Amgen
INDUSTRY