Abstract | BACKGROUND: OBJECTIVE: To evaluate bleeding and thrombotic events occurring in chronic ITP patients during two phase 3, randomized, placebo-controlled, 24-week studies of romiplostim and during subsequent treatment in an open-label extension study. PATIENTS/METHODS: In the phase 3 trials, 125 patients were randomized to romiplostim or placebo; romiplostim dose was adjusted to maintain platelet counts of 50-200 x 10(9) L(-1). Patients who completed the phase 3 trials could enroll in the extension study in which all patients received romiplostim. RESULTS: In the phase 3 trials, a significantly greater percentage of patients treated with placebo (34%) had bleeding adverse events of moderate or greater severity than did patients treated with romiplostim (15%, P = 0.018). In the extension study, the incidence of bleeding adverse events of moderate or greater severity decreased from 23% of patients in the first 24 weeks to 12% after 24-48 weeks, remaining < or = 6% thereafter. The exposure-adjusted incidence of thrombotic events was 0.1 per 100 patient-weeks in the phase 3 studies, and 0.08 per 100 patient-weeks in the extension study where patients received romiplostim for up to 144 additional weeks. CONCLUSIONS: The incidence and severity of bleeding was decreased in chronic ITP patients treated with romiplostim compared with placebo, and the incidence of thrombotic events was not different between the two groups.
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Authors | T B Gernsheimer, J N George, L M Aledort, M D Tarantino, U Sunkara, D Matthew Guo, J L Nichol |
Journal | Journal of thrombosis and haemostasis : JTH
(J Thromb Haemost)
Vol. 8
Issue 6
Pg. 1372-82
(Jun 2010)
ISSN: 1538-7836 [Electronic] England |
PMID | 20230419
(Publication Type: Clinical Trial, Phase III, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Chemical References |
- Placebos
- Receptors, Fc
- Receptors, Thrombopoietin
- Recombinant Fusion Proteins
- Thrombopoietin
- romiplostim
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Topics |
- Chronic Disease
- Double-Blind Method
- Hemorrhage
(chemically induced)
- Humans
- Placebos
- Prospective Studies
- Receptors, Fc
(therapeutic use)
- Receptors, Thrombopoietin
(agonists)
- Recombinant Fusion Proteins
(adverse effects, therapeutic use)
- Thrombocytopenia
(drug therapy, physiopathology)
- Thrombopoietin
(adverse effects, therapeutic use)
- Thrombosis
(chemically induced)
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