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Xin Du,Daobin Zhou
Frontiers of Medicine 2016, Volume 10, Issue 4, Pages 437-443 doi: 10.1007/s11684-016-0472-9
A phase II study (A2202) was performed to evaluate the efficacy and safety of JAK inhibitor ruxolitinibRuxolitinib was given twice a day (bid) at a starting dose of 15 mg (n=25) or 20 mg (n=debilitating constitutional symptoms, as assessed by MFSAF v2.0, was observed in patients treated with ruxolitinibRuxolitinib treatment was generally well tolerated by Chinese patients.Ruxolitinib provided substantial reductions in splenomegaly and improvements in symptoms, and was well-tolerated
Keywords: JAK ruxolitinib Chinese patients myelofibrosis
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